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Cardiovascular outcomes trials: a paradigm shift in the current management of type 2 diabetes
Cardiovascular Diabetology volume 21, Article number: 144 (2022)
Cardiovascular disease (CVD) is the leading cause of mortality and morbidity in patients with type 2 diabetes (T2D). Historical concerns about cardiovascular (CV) risks associated with certain glucose-lowering medications gave rise to the introduction of cardiovascular outcomes trials (CVOTs). Initially implemented to help monitor the CV safety of glucose-lowering drugs in patients with T2D, who either had established CVD or were at high risk of CVD, data that emerged from some of these trials started to show benefits. Alongside the anticipated CV safety of many of these agents, evidence for certain sodium–glucose transporter 2 (SGLT2) inhibitors and glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have revealed potential cardioprotective effects in patients with T2D who are at high risk of CVD events. Reductions in 3-point major adverse CV events (3P-MACE) and CV death have been noted in some of these CVOTs, with additional benefits including reduced risks of hospitalisation for heart failure, progression of renal disease, and all-cause mortality. These new data are leading to a paradigm shift in the current management of T2D, with international guidelines now prioritising SGLT2 inhibitors and/or GLP-1 RAs in certain patient populations. However, clinicians are faced with a large volume of CVOT data when seeking to use this evidence base to bring opportunities to improve CV, heart failure and renal outcomes, and even reduce mortality, in their patients with T2D. The aim of this review is to provide an in-depth summary of CVOT data—crystallising the key findings, from safety to efficacy—and to offer a practical perspective for physicians. Finally, we discuss the next steps for the post-CVOT era, with ongoing studies that may further transform clinical practice and improve outcomes for people with T2D, heart failure or renal disease.
The prevalence of type 2 diabetes (T2D) has continued to rise over recent years. It is estimated that by 2045 there will be 693 million people diagnosed with the condition worldwide . T2D poses significant health risks to individuals, with a two-fold increase in mortality compared with a population without diabetes , as well as an increasing global health economic burden . Associations between T2D and cardiovascular disease (CVD) are well established; CVD is the leading cause of mortality and morbidity in patients with T2D [2,3,4], and more than 30% of patients with T2D are diagnosed with CVD . The most common CVD manifestations in patients with T2D are peripheral arterial disease, ischaemic stroke, stable angina, heart failure (HF) and nonfatal myocardial infarction (MI) [3, 5]. A recent meta-analysis showed that patients with coexisting diabetes and HF have an increased risk of all-cause death, cardiovascular (CV) death and hospitalisation . Moreover, one in six patients with newly diagnosed T2D have evidence of silent MI associated with an increased risk of all-cause mortality (HR 1.26, 95% CI 1.06–1.50) and fatal MI (HR 1.49, 95% CI 1.15–1.94) . Reducing CV risk is a key part of T2D disease management .
Until around a decade ago, the standard of care for T2D involved the use of glucose-lowering drugs (GLDs) such as metformin, sulfonylureas, thiazolidinediones, meglitinides and α-glucosidase inhibitors . However, amid uncertainty about the CV safety of GLDs [9,10,11,12], in 2008 the U.S. Food and Drug Administration (FDA) updated its guidance, mandating the assessment of all new T2D therapies in long-term CV outcomes trials (CVOTs), in addition to the requirement for registrational studies demonstrating improvements in glycaemic control . In the meantime, newer GLD classes have become firmly established treatments for T2D, i.e. dipeptidyl peptidase-4 (DPP-4) inhibitors, glucagon like peptide-1 receptor agonists (GLP-1 RA) and sodium–glucose cotransporter-2 (SGLT2) inhibitors. To date, 18 CVOTs have been published for these newer GLDs (Fig. 1), which enrolled patients with T2D who had established CVD or were at high risk of CVD [13,14,15,16,17,18,19,20,21,22,23,24], and had to demonstrate a hazard ratio (HR) < 1.8 for major CV events (MACE; based on the upper bound of a two-sided 95% confidence interval [CI]). Most CVOTs included the key composite outcome of 3-point MACE (3P-MACE; comprising CV death, nonfatal MI and nonfatal stroke), with the exceptions of additional events in a 4P-MACE in the ELIXA trial of lixisenatide (hospitalisation for unstable angina) and in the AMPLITUDE-O trial of efpeglenatide (death from undetermined causes) [10, 25, 26]. Notably, some CVOTs have not only illustrated CV safety, but also reported cardioprotective benefits. The first of these was EMPA-REG OUTCOME, completed in 2015, which showed that the SGLT2 inhibitor empagliflozin reduced 3P-MACE and CV death in patients with T2D and established CVD . Hospitalisation for heart failure (HHF), all-cause mortality and progression of kidney disease were also reduced with empagliflozin [27,28,29]. Subsequently published CVOTs, as well as a small number of HF and renal outcomes studies, have added further paradigm-shifting evidence for improvements in CV, HHF and renal outcomes during treatment with other GLDs, such as the SGLT2 inhibitor canagliflozin, in patients with T2D (Table 1; Additional file 1: Table S1) [15, 16, 27, 30,31,32,33,34,35,36,37]. CVOT findings are now a major focus of updated treatment guidelines (Table 2) [38,39,40,41,42,43,44] and product labels .
The purpose of this review is to provide an expert summary that will help clinicians navigate the overwhelming wealth of CVOT data. We discuss how CVOTs can provide valuable insights for management in clinical practice, and consider remaining gaps in knowledge, as well as how diabetes CVOTs have led to further cardiorenal-focussed studies that seek to understand more about how some GLDs may improve outcomes for our patients.
Can we compare diabetes CVOTs?
In the absence of head-to-head studies, caution must be exercised when interpreting data from indirect comparison of CVOTs. Among the potential heterogeneity in trial designs and baseline characteristics, particular attention should be paid to differing baseline criteria for CVD diagnosis and CV risk in trial cohorts; patients with established CVD or CV risk factors at baseline may be more likely to progress through the continuum of CVD . The proportions of patients with established CVD varied substantially between the CVOTs. For instance, all patients in ELIXA had established CVD, compared with 31–83% in LEADER, SUSTAIN-6 and REWIND (Additional file 2: Figure S1). Other key baseline characteristics that varied substantially between the CVOTs included HF diagnosis and renal impairment. There have also been suggestions of differing outcomes by region or race/ethnicity in the CVOTs, and in the HF and renal outcome trials, although these studies were not powered to reliably detect differences between subgroups [27, 30, 32, 46]. For instance, as recently reported for the LEADER CVOT of the GLP-1 RA liraglutide, 3P-MACE HR (95% CI) ranged from 0.62 (0.37–1.04) in Asia to 1.01 (0.84–1.22) in North America, although there was a lack of clear statistical evidence of interaction between regions and the outcome (p = 0.20) [32, 47]. The task of assessing the profile of CV risk in CVOT populations is also complicated by the prevalence of unrecognised diabetic cardiac impairment in patients with T2D, which may include ischaemia, myocardial dysfunction and/or cardiac arrhythmia presenting with atypical symptoms . However, it is notable that post hoc analyses of EMPA-REG OUTCOME showed consistency of CV benefits with empagliflozin across patients with different baseline CV risk factors, including prior MI , prior stroke , Thrombolysis In Myocardial Infarction (TIMI) score , prior coronary artery bypass graft surgery , left ventricular hypertrophy , peripheral artery disease  and atrial fibrillation . Canagliflozin has also shown consistency in CV outcomes across subgroups, including in patients with different levels of albuminuria , and enhanced 3P-MACE in patients with prior diuretic usage .
From CV safety to CV efficacy in patients with T2D
DPP-4 inhibitors: no evidence for cardioprotection
The first T2D CVOTs to be reported, SAVOR-TIMI 53 and EXAMINE, assessed the CV safety of the DPP-4 inhibitors saxagliptin and alogliptin, respectively. Before publication of these two CVOTs in 2013, post hoc analyses of phase 2 and 3 trials suggested a trend for lower incidence of major CV events with DPP-4 inhibitors than with placebo or other comparators . Similarly, both CVOTs demonstrated non-inferiority in 3P-MACE for saxagliptin (HR [95% CI] 1.00 [0.89–1.12]) and alogliptin (HR [95% CI] 0.96 [upper < 1.16]), compared with placebo (Additional file 1: Table S1) [57, 58]. However, saxagliptin had a significantly elevated risk of HHF compared with placebo (HR [95% CI] 1.27 [1.07–1.51], p < 0.01)  and there was a suggestion of increased risk of HHF in patients treated with alogliptin vs placebo (HR [95% CI] 1.19 [0.90–1.58]), which led to the FDA issuing a safety warning for both alogliptin and saxagliptin . Overall, subsequent CVOTs for DPP-4 inhibitors (sitagliptin and linagliptin) have demonstrated acceptable CV safety, consistently showing a neutral effect on 3P-MACE [13, 14, 60]. CARMELINA (linagliptin) included a cohort with a majority of patients presenting with prevalent chronic kidney disease (CKD) at baseline (mean estimated glomerular filtration rate [eGFR], 55 mL/min/1.73 m2) . In the CAROLINA CVOT (mean eGFR at baseline, 77 mL/min/1.73 m2), linagliptin was non-inferior to glimepiride, based on 3P-MACE .
SGLT2 inhibitors: cardioprotection with empagliflozin and canagliflozin
Cardioprotective benefits of GLDs were first observed in the EMPA-REG OUTCOME trial, in which the SGLT2 inhibitor empagliflozin showed a 14% reduction in the risk of 3P-MACE compared with placebo (HR [95% CI] 0.86 [0.74–0.99], p = 0.04) in patients with T2D and established CVD . Among the components of 3P-MACE, the risk of CV death was reduced by 38% with empagliflozin (HR [95% CI] 0.62 [0.49–0.77], p < 0.001), while the impact on each of nonfatal stroke and nonfatal MI was neutral  (Table 1; Additional file 1: Table S1).
The canagliflozin CVOT programme, comprising CANVAS and CANVAS-R, also demonstrated a 14% reduction in 3P-MACE (HR [95% CI] 0.86 [0.75–0.97], p = 0.02) in patients with established CVD or high CV risk, although no significant reduction in CV deaths (HR [95% CI] 0.87 [0.72–1.06]) . The beneficial effect of canagliflozin on 3P-MACE was confirmed in patients with T2D and CKD in a subsequent renal outcomes trial, CREDENCE (HR [95% CI] 0.80 [0.67–0.95], p = 0.01), which also showed a trend towards a reduction in CV deaths that neared significance (HR [95% CI] 0.78 [0.61–1.00], p = 0.05) . CKD in patients with T2D has been strongly linked to CV events and mortality in CVOTs , although the prevalence of CKD in diabetes CVOTs was typically much lower than in CREDENCE [14, 36].
A recently reported meta-analysis of 11 clinical trials demonstrated cardiorenal benefits across the SGLT2 inhibitor class versus placebo. CV benefits included a 12% reduction in 3P-MACE (without significant heterogeneity; I2 = 21.2%, p = 0.19), based on six cardiorenal studies that reported this outcome, and a 16% reduction in CV death . However, these results should be caveated; there were differences in outcomes, study designs, patient populations, and medications across the cardiorenal studies included in the meta-analysis. The 12% reduction in 3P-MACE was based on data from EMPA-REG OUTCOME, CANVAS, CREDENCE, DECLARE-TIMI 58 (dapagliflozin), VERTIS CV (ertugliflozin) and SCORED (sotagliflozin). Notably, sotagliflozin has both SGLT1 and SGLT2 inhibitory activity and is not a licensed treatment for T2D (but is licensed for type 1 diabetes in Europe), and SCORED was a cardiorenal study (patients had T2D and CKD) that used a different 3P-MACE outcome (CV death, HHF and urgent visits for HF) than the other studies (CV death, nonfatal MI and nonfatal stroke). The dapagliflozin CVOT, DECLARE-TIMI 58, did not show a benefit in either 3P-MACE (HR [95% CI] 0.93 [0.84–1.03], p = 0.17) or CV deaths (0.98 [0.82–1.17]) [37, 62]. However, DECLARE-TIMI 58 had a very different profile of baseline characteristics to EMPA-REG OUTCOME and CANVAS, as a majority of patients had high CV risk but not established CVD, and there were fewer patients with CKD . Therefore, the different outcomes in DECLARE-TIMI 58, compared with EMPA-REG OUTCOME and CANVAS, may be due to differences in study design and cohort composition rather than intrinsic differences between the study drugs. Two HF and renal outcomes studies, designed to assess the effect of dapagliflozin vs placebo in patients with HF with reduced ejection fraction (HFrEF; DAPA-HF) or CKD (DAPA-CKD) with or without T2D, both reported trends towards reductions in CV death in the T2D subgroups (HR [95% CI] 0.79 [0.63–1.01] and 0.85 [0.59–1.21], respectively) [63, 64]. In the VERTIS CV study of ertugliflozin, all patients had established CVD at baseline, but no benefit was observed in 3P-MACE (HR [95% CI] 0.97 [0.85–1.11]) or CV death (HR [95% CI] 0.92 [0.77–1.11]) . These findings suggest that significant improvements in CV outcomes, which were observed in CVOTs of empagliflozin and canagliflozin, may not apply to all SGLT2 inhibitors.
GLP-1 RAs: cardioprotection with subcutaneous and long acting GLP-1 RAs, but inconclusive evidence for short-acting and oral long-acting medications
A meta-analysis of eight CVOTs recently demonstrated reductions in 3P/4P-MACE and CV death of 14% and 13%, respectively, across the GLP-1 RA class, compared with placebo . These findings were based on data from five studies of subcutaneously administered long-acting GLP-1 RAs (AMPLITUDE-O, LEADER, SUSTAIN-6, REWIND, and HARMONY OUTCOMES), a study of orally administered long-acting semaglutide (PIONEER-6) and two studies of subcutaneously administered short-acting GLP-1 RAs (ELIXA, EXSCEL). The FREEDOM-CVO non-inferiority study of continuously infused exenatide, which recently showed no CV benefits over placebo based on the primary outcome of 4P-MACE (HR [95% CI] 1.21 [0.90–1.63]), 3P-MACE and their individual component outcomes  (Additional file 1: Table S1), was not included in the meta-analysis.
Significant reductions in 3P/4P-MACE have been reported for all five of the CVOTs of subcutaneously administered long-acting GLP-1 RAs, including the recently reported AMPLITUDE-O study (efpeglenatide; HR [95% CI] 0.73 [0.58–0.92]; p < 0.01), LEADER (liraglutide; 0.87 [0.78–0.97], p = 0.01), SUSTAIN-6 (semaglutide; 0.74 [0.58–0.95], p = 0.02), REWIND (dulaglutide; 0.88 [0.79–0.99], p = 0.03), and HARMONY OUTCOMES (albiglutide; 0.78 [0.68–0.90], p < 0.01) (Table 1) [31, 32, 34, 35]. The latter GLP-1 RA, albiglutide, is no longer commercially available.
When the oral formulation of semaglutide was compared with placebo in the PIONEER-6 trial , a trend was observed towards reduction in 3P-MACE (HR [95% CI] 0.79 [0.57–1.11], p = 0.17). However, PIONEER-6 was a small study (N = 3183) of short duration, designed to rule out excess risk of 3P-MACE, and not powered to demonstrate superiority . Based on clinicaltrials.gov, a large CVOT investigating an oral formulation of semaglutide, the SOUL trial, is underway (estimated N = 9642). Primary and study completion are scheduled for July 2024.
Across the long-acting GLP-1 RA CVOTs, the outcomes for individual components of 3P-MACE were much less uniform than for the composite endpoint: only two of the five trials demonstrated a significant reduction in CV death, LEADER (liraglutide; HR [95% CI] 0.78 [0.66–0.93], p = 0.01) and PIONEER-6 (oral semaglutide; HR [95% CI] 0.49 [0.27–0.92], p = 0.03) [15, 32, 66]; however, neither study showed a significant reduction in nonfatal stroke or nonfatal MI, whereas SUSTAIN-6 (semaglutide) and REWIND (dulaglutide) significantly reduced the risk of nonfatal stroke, while HARMONY OUTCOMES (albiglutide) significantly reduced the risk of fatal or nonfatal MI [31, 34, 35].
Unlike the findings for long-acting GLP-1 RAs, the short-acting GLP-1 RA lixisenatide showed no significant CV benefits in the ELIXA study, taking into account 4P-MACE (HR [95% CI] 1.02 [0.89–1.17]; p = 0.81), its individual components, and HHF  (Additional file 1: Table S1). The EXSCEL study of prolonged-release exenatide, another short-acting GLP-1 RA, showed a trend towards a reduction in 3P-MACE that neared significance (HR [95% CI] 0.91 [0.83–1.00], p = 0.06)  although, as previously mentioned, no CV benefits were observed for continuously infused exenatide in the FREEDOM-CVO trial . In addition to the possibility of patients’ baseline characteristics affecting study outcomes, the differing results of the long- and short-acting GLP-1 RA CVOTs suggest that the kinetics of both receptor agonism and drug exposure may play roles in conferring cardioprotection. More research is needed to determine whether the documented differences between the pharmacokinetics, delivery and effects of short- and long-acting GLP-1 RAs  translate into differences in CV outcomes.
Can modern glucose-lowering drugs reduce all-cause mortality?
The data emerging from CVOTs means that clinicians can, for the first time, consider therapeutic options among GLDs that may reduce mortality and improve CV outcomes in certain patient groups. Unlike DPP-4 inhibitors, SGLT2 inhibitors and some GLP-1 RAs are associated with significant reductions in all-cause mortality (Table 1 and Additional file 1: Table S1).
SGLT2 inhibitors: evidence for reduced all-cause mortality
No significant reduction of all-cause death with dapagliflozin was seen in DECLARE-TIMI 58 (HR [95% CI] 0.93 [0.82–1.04]) . However, reductions in all-cause death were observed in DAPA-HF (HR [95% CI] 0.83 [0.71–0.97]) and in DAPA-CKD (0.69 [0.53–0.88]), in populations of patients with HFrEF or CKD, with or without T2D. These reductions in all-cause death were compatible with CV death outcomes in DAPA-HF (HR [95% CI] 0.82 [0.69–0.98]) and in DAPA-CKD (0.81 [0.58–1.12]) [68, 69].
Notably, EMPA-REG OUTCOME (empagliflozin) demonstrated a significantly reduced all-cause death rate (HR [95% CI] 0.68 [0.57–0.82]) (Additional file 1: Table S1), which was primarily driven by a reduced risk of CV death (Table 1) [27, 32]. Another study, EMPEROR-Reduced, was designed to assess the effect of empagliflozin vs placebo in patients with HFrEF, with or without T2D. In this patient population, trends towards reductions in CV death were reported in patients with T2D (HR [95% CI] 0.92 [0.71–1.20]) and without T2D (0.92 [0.68–1.24]) .
In the canagliflozin diabetes CVOT programme (CANVAS and CANVAS-R), no statistically significant reductions were detected in all-cause mortality (HR [95% CI] 0.87 [0.74–1.01]) or CV deaths (0.87 [0.72–1.06]) in patients with T2D .
GLP-1 RAs: evidence for reduced all-cause mortality
The LEADER CVOT demonstrated significantly reduced all-cause mortality with liraglutide vs placebo (HR [95% CI] 0.85 [0.74–0.97]) (Additional file 1: Table S1), compatible with reduced risk of CV death (Table 1) [27, 32]. A reduced risk of all-cause death in patients with T2D was also noted in EXSCEL (exenatide) (HR [95% CI] 0.86 [0.77–0.97]) and PIONEER-6 (oral semaglutide) (0.51 [0.31–0.84]), although these results were only nominally significant, owing to the hierarchical testing plans used [15, 33]. These reductions in all-cause death were accompanied by a trend towards reduction in CV death in EXSCEL (HR [95% CI] 0.88 [0.76–1.02]) and, as previously mentioned, by significant reduction in PIONEER-6 (0.49 [0.27–0.92], p = 0.03) (Additional file 1: Table S1).
Similarly, in the recently published AMPLITUDE-O CVOT (efpeglenatide), the trend towards reduction in CV death (HR [95% CI] 0.72 [0.50–1.03]) was compatible with all-cause mortality (0.78 [0.58–1.06]).
Treatment recommendations in relation to CV benefits and reduced all-cause mortality
In light of the significant benefits of certain SGLT2 inhibitors and GLP-1 RAs in reducing the risks of CV death and all-cause death in patients with T2D, major international guidelines have been updated to include evidence from CVOTs to help differentiate between the use of GLDs. The American College of Cardiology (ACC) , American Diabetes Association (ADA) and European Association for the Study of Diabetes (EASD) [42, 44], and the Europe Society of Cardiology (ESC) and EASD  guidelines all recommend specific treatments for patients with T2D and atherosclerotic CVD (ASCVD) based on CVOT data (Table 2). The general consensus between the guidelines is that patients diagnosed with T2D and CVD should be treated with an SGLT2 inhibitor or GLP-1 RA with proven CVD benefit, either as first add-on to metformin or as monotherapy. The ESC guidelines specifically recommend use of empagliflozin in patients with T2D and CVD to reduce the risk of death, while empagliflozin, canagliflozin, or dapagliflozin are recommended in patients with T2D and CVD, or at very high/high CV risk, to reduce CV events . Regarding choice of GLP-1 RA, the ESC and ACC guidelines recommend the use of dulaglutide, liraglutide or injectable semaglutide for patients with T2D and CVD, based on their CV benefits [38,39,40, 43].
Beyond MACE: HF and renal findings
Many CVOTs have reported beyond the mandated 3P-MACE outcomes, elucidating additional benefits seen with some GLDs, including reducing the risk of HHF and slowing the progression of renal disease. For the most part, these have been secondary outcomes, although complementary dedicated HF and renal outcomes studies that included patients with and without T2D have recently been published for SGLT2 inhibitors [18, 36, 68, 69, 71, 72], while large-scale real-world outcomes studies have provided further insights [73,74,75,76,77,78,79,80,81,82].
SGLT2 inhibitors: evidence for reduced risk of HHF
Both dapagliflozin and empagliflozin are approved in Europe and the US for the treatment of patients with chronic HFrEF, based on published findings of dedicated HF outcomes studies, DAPA-HF and EMPEROR-Reduced (Fig. 2A, B) [69, 71, 83, 84]. In February and March 2022, empagliflozin also received FDA and European Commission approval for the treatment of patients with preserved EF (HFpEF), in light of encouraging findings from the recently reported EMPEROR-Preserved trial [85, 86], while the DELIVER trial of dapagliflozin in patients with HFpEF is ongoing . The recently completed EMPEROR-Preserved and ongoing DELIVER trials are covered in the ‘Where Next?’ section of this review.
In the DAPA-HF cohort of patients with HFrEF, only 40% of which had comorbid T2D, the relative risk reduction (RRR) for HHF was 30% with dapagliflozin in the overall population (Additional file 1: Table S1) ; when looking only at patients with T2D, the RRR observed was 24% . Very similar results were seen with empagliflozin in patients with HFrEF in EMPEROR-Reduced, with RRR of 31% in HHF for all patients and 33% when only looking at those with T2D [70, 71]. The results of a recent meta-analysis of patients with HFrEF from DAPA-HF and EMPEROR-Reduced demonstrated consistent CV benefits, based on a composite of HHF and CV death, for a range of patient subgroups including those with or without T2D and regardless of baseline eGFR (i.e. above or below 60 mL/min/1.73 m3) . The protection from HHF offered by SGLT2 inhibitors has now been reflected in international guidelines [38, 40, 42] and in several real-world studies (Fig. 2D) [73, 74, 77,78,79,80, 89, 90].
In addition to dedicated HF outcomes studies, a reduced risk of HHF in patients with T2D has also been demonstrated consistently in diabetes CVOTs and in renal outcomes studies across a range of SGLT2 inhibitors, including empagliflozin (EMPA-REG OUTCOME, RRR 35%) , canagliflozin (CANVAS/CANVAS-R, RRR 33%; CREDENCE, RRR 39%) [30, 36], dapagliflozin (DECLARE-TIMI 58, RRR 27%)  and ertugliflozin (VERTIS CV, RRR 30%) (Fig. 2A) . Indirect comparison of these findings is hampered by baseline HF not being well characterised in the CVOT patient cohorts, by variation in baseline characteristics between studies, and by lack of power to detect an impact on HHF. For instance, across the SGLT2 inhibitor CVOTs, the proportion of patients with HF diagnosed at baseline ranged from 10% in EMPA-REG OUTCOME to 24% in VERTIS CV (Fig. 2B; Additional file 1: Table S1) [16, 27, 30, 36, 37]. Nevertheless, these shortcomings have been at least partly overcome by dedicated HF outcomes trials.
SGLT2 inhibitors: evidence for renal benefits
Dapagliflozin recently became the first SGLT2 inhibitor approved in Europe for the treatment of patients with CKD, regardless of diabetes status, based on findings from the DAPA-CKD renal outcomes trial. Adding dapagliflozin to standard care was associated with significantly lower risk (HR [95% CI] 0.61 [0.51–0.72], p < 0.001) of a composite cardiorenal outcome (sustained decline in the eGFR of ≥ 50%, end-stage kidney disease, or death from renal or CV causes) and other renal benefits (Fig. 3A) [68, 91]. Another dedicated renal outcomes study (CREDENCE), in patients with T2D and comorbid CKD, also confirmed the profile of renal benefits with canagliflozin suggested by the CANVAS diabetes CVOT programme (Fig. 3A) . Improved renal outcomes have been noted consistently across CVOTs for SGLT2 inhibitors, both in terms of renal function and albuminuria. RRR in renal function outcomes were ≥ 35% across the class (Fig. 3A) [28, 36, 37, 92,93,94]. Progression of albuminuria was also consistently slowed with SGLT2 inhibitors (Fig. 3A) [28, 30, 36, 93, 95]. In the SCORED cardiorenal study (sotagliflozin), there was a trend towards benefit (HR [95% CI] 0.71 [0.46–1.08]) for a composite of renal outcomes (first occurrence of a sustained decrease of ≥ 50% in eGFR from baseline for ≥ 30 days, long-term dialysis, renal transplantation, or sustained eGFR of < 15 mL/min/1.73 m2 for ≥ 30 days) in patients with T2D and comorbid CKD . Note that sotagliflozin is not a licensed treatment for T2D and has both SGLT1 and SGLT2 inhibitory activity.
GLP-1 RAs: potential reduction in HHF and evidence for some renal benefits
While GLP-1 RA CVOTs demonstrated improvements in some renal outcomes relating to albuminuria, neutral effects were typically seen on the hard endpoint of renal function (Fig. 3A) and, when reported, on HHF (Additional file 1: Table S1) [23, 31, 34, 96]. However, the recently published AMPLITUDE-O CVOT demonstrated RRRs of 39% for HF, 32% for incident macroalbuminuria, and 32% for a composite renal outcome (incident macroalbuminuria, ≥ 30% increase in UACR from baseline, sustained ≥ 40% decrease in eGFR for ≥ 30 days, renal-replacement therapy for ≥ 90 days, and sustained eGFR of < 15 mL/min/1.73 m2 for ≥ 30 days) with efpeglenatide vs placebo . A trend towards a decrease with efpeglenatide (HR [95% CI] 0.77 [0.57–1.02], p = 0.07) was reported for another renal composite outcome (≥ 40% decrease in eGFR for ≥ 30 days, end-stage kidney disease, or death from any cause) . REWIND (dulaglutide) also showed benefits for some, but not all, measures of kidney function .
DPP-4 inhibitors: neutral effect on HHF, in general, and evidence for modest renal benefits
CVOTs investigating DPP-4 inhibitors have generally shown neutral effects on HHF and modest renal benefits in terms of reduced albuminuria [20, 98,99,100]. In CARMELINA, linagliptin demonstrated a modest reduction in time to first occurrence of albuminuria progression vs placebo (RRR 14%) (Fig. 3A) . In SAVOR-TIMI 53, saxagliptin showed beneficial albuminuria results (RRR not reported)  but also an elevation in HHF , while EXAMINE (alogliptin) reported a trend towards increased HHF .
Treatment recommendations in relation to HF and renal benefits
The prevalence of renal impairment across diabetes CVOTs varied considerably, being particularly high in CARMELINA (linagliptin), hampering conclusions about how renal effects may compare between GLDs (Fig. 3B) [14, 20, 101]. However, the totality of evidence from CVOTs and renal outcomes studies shows conclusively that patients with T2D experience superior renal benefits with SGLT2 inhibitors than with DPP-4 inhibitors and currently approved GLP-1 RAs.
Moreover, despite the limitations of CVOTs for assessing HF and renal outcomes, the evidence for HF and renal benefits with SGLT2 inhibitors was deemed sufficient by professional societies to update guidelines, even before the emergence of results from dedicated HF and renal studies. As such, SGLT2 inhibitors are recommended as either first add-on, concomitant to metformin, or as a monotherapy in patients with T2D and HF or CKD in guidelines that include the ADA and EASD joint Consensus Report on the Management of Hyperglycaemia 2019 , the ADA’s Standards of Medical Care in Diabetes 2022 , the European Renal Association (ERA)—European Dialysis and Transplant Association (EDTA) 2019 guidelines , and the Kidney Disease Improving Global Outcomes (KDIGO) 2020 guidelines on diabetes management in CKD  (Figs. 2C, 3C).
Other clinical considerations
In addition to considering the impact of GLDs on cardiorenal outcomes from CVOTs and related studies, there are also other practical reasons to prescribe DPP-4 inhibitors, GLP-1 RAs, and SGLT2 inhibitors. For instance, all three therapeutic classes are associated with relatively low risk of hypoglycaemic events, while patients treated GLP-1 RAs and SGLT2 inhibitors may benefit from weight loss [15, 27, 30, 32, 57, 103].
Clinical inertia to the use of SGLT2 inhibitors and GLP-1 RAs
Many patients with CV risk still do not receive SGLT2 inhibitors or GLP-1 RAs as part of their GLD regimen, even though these medications are recommended for CVD prevention in the treatment guidelines. DPP-4 inhibitors are more widely used than SGLT2 inhibitors or GLP-1 RAs, despite comparable costs to SGLT2 inhibitors and the lack of evidence that DPP-4 inhibitors improve cardiorenal outcomes . The successful implementation of CVOT insights and new guidelines into clinical practice, and consequent improvements in patient outcomes, will rely heavily on implementation programmes and educational tools [38, 105].
Despite significant advancements in the treatment strategies available to patients with T2D (and endorsement in updated guidelines), outstanding questions are being addressed by ongoing research. Given that some CVOTs have populations entirely (or almost entirely) comprised of patients with established CVD, while other CVOTs also included patients at high risk of CVD events, greater insight into cardiorenal outcomes in these respective patient groups would be beneficial. Additional efficacy data for other patient subgroups would also be welcome, including investigation of potential differences in CV outcomes by region/ethnicity , and further investigation of GLDs in populations without T2D. Questions also remain regarding cost-effectiveness in particular patient subgroups, although SGLT2 inhibitors, GLP-1 RAs and DPP-4 inhibitors are generally considered to be cost-effective compared with insulin, thiazolidinediones and sulfonylureas in patients with T2D [106, 107].
Another avenue being explored is the potential value of combining different classes of GLD therapies; SGLT2 inhibition combined with GLP-1 RAs may have synergistic effects on HbA1c level, blood pressure, body weight, and CV outcomes [108, 109]. Regarding combination therapy with metformin, results from the GRADE randomised trial were presented at the EASD 2021 annual meeting; patients (N = 5047) received either glimepiride (sulfonylurea), sitagliptin (DPP-4 inhibitor), liraglutide (GLP-1 RA), or insulin glargine (clinicaltrials.gov identifier: NCT01794143). Incidence of CVD (MACE, HHF, unstable angina, revascularisation) was lowest with liraglutide, while microvascular (kidney and neuropathy) outcomes were comparable across the four treatment groups. The worst metabolic outcomes were observed with the combination of sitagliptin and metformin; the sitagliptin and glimepiride groups both met the primary outcome (≥ 7% HbA1c) more frequently, and earlier in time, than the glargine and liraglutide groups. Conversely, it is worth noting that linagliptin, another DPP-4 inhibitor, was significantly better than glimepiride regarding two key metabolic outcomes in the CAROLINA CVOT (both were composite outcomes that included maintenance of HbA1c at ≤ 7.0%, without > 2% weight gain) .
Elucidating mechanisms of action in relation to cardiorenal protection
Questions remain about the mechanism of action of SGLT2 inhibitors and GLP-RAs, particularly in relation to the cardiorenal benefits observed in some diabetes CVOTs [110,111,112] (Additional file 2: Fig. S2). Cardio- and reno-protective effects are unlikely to be solely explained by the mechanisms used by these drugs to lower blood glucose levels, as the same effects are not seen with drugs that have stronger antihyperglycaemic actions , and were not dependent upon the degree of HbA1c reduction [113,114,115]. Moreover, while direct comparisons cannot be made without head-to-head trials, some outcomes in diabetes CVOTs have been within the range expected for cardiorenal therapies such as statins, aspirin and antihypertensives , despite being added on top of a standard of care that often included these therapies (Fig. 4). Consequently, new theories around the modes of action for SGLT2 inhibitors and GLP-1 RAs are being hypothesised [112, 117,118,119], although as yet it remains unclear which mechanism(s) are responsible, or whether there is any mechanistic overlap between cardiorenal benefits with SGLT2 inhibitors and GLP-1 RAs.
Proposed, sometimes contradictory, mechanisms for cardiorenal protective effects with SGLT2 inhibitors include enhancement of fuel supply through the production of ketones (the “thrifty substrate” hypothesis) [118, 119]; an induction of tissue-protective, energy-preserving metabolic states similar to those seen with animal hibernation [112, 117]; haemodynamic volume effects (SGLT2 inhibitors are predicted to produce a twofold greater reduction in interstitial fluid volume compared with blood volume) ; improved cardiac remodelling, increased provascular progenitor cells and decreased ischaemia/reperfusion injury ; off-target inhibition of the cardiac Na+/H+ exchanger, thus reducing cardiac cytosolic sodium in animal models ; and possible direct influences of SGLT2 inhibitors on inflammatory responses . More exhaustive lists of speculated mechanisms have been reviewed elsewhere .
For GLP-1 RAs, proposed mechanisms of action include an anti-atherothrombotic effect, as well as amelioration of inflammatory markers, resulting in the enhanced retardation of atherosclerosis [60, 124].
Recently completed and ongoing HF and renal studies
Recently completed and ongoing dedicated HF and renal studies (Fig. 5A) will provide more evidence on each agent to inform clinical decisions where reducing CV, HF or renal risk is a consideration. Similarly, by including both patients with and without T2D (Fig. 5B, C), these studies suggest that patients without T2D can benefit from certain GLDs where they have a history of HF or CKD [13, 36, 69, 125, 126]—however, evidence from these studies will remain relevant to patients with T2D and their treating physicians, due to the prevalence of comorbid HF and CKD and the CV–renal–metabolic axis .
Among ongoing and recently completed HF outcomes trials, studies on patients with HFpEF (Figs. 2A, B and 5C) such as EMPEROR-Preserved phase 3 trial , are of particular interest, as no agent of any class has previously shown a clear and unambiguous benefit for this indication . Notably, EMPEROR-Preserved recently met its primary endpoint—empagliflozin significantly reduced the risk of the composite of CV death and HHF in adults with HFpEF > 40%, with or without diabetes [85, 86]. Reductions in the risk of various HF events were observed for inpatients and outpatients . Although empagliflozin appeared to have less of a reno-protective effect in patients with HFpEF than with HFrEF, further analyses of EMPEROR-Preserved indicate that this may be related to the endpoint definition used (which excluded renal death and included ≥ 40% decrease in eGFR), with positive findings when using the renal endpoint from the DAPA-HF trial (which included renal death and ≥ 50% decrease in eGFR) [130, 131]. In an editorial, the author noted that findings for dapagliflozin in the DELIVER trial, in patients with HFpEF > 40%, are also keenly awaited .
Exploring the full potential of SGLT2 inhibitors and GLP-1 RAs: differentiating between clinical trials and the need for real-world evidence
As evidence from renal and HF outcomes studies emerges to add to the wealth of data from CVOTs, the challenge will be to integrate the learnings from an ever-increasing number of studies, and from disparate populations, into clinical practice. Clinicians are faced with untangling many differences in trial design and patient characteristics, and an absence of any direct head-to-head insights. When making evidence-based therapy decisions, it is important to consider trials with relevant study populations, and in particular to bear in mind patients’ diabetes status, as well as CV, HF and renal risk (i.e. factors that should be reflected by licensing approvals for individual medications and up-to-date treatment guidelines). For example, many patients in dedicated HF studies do not have diabetes and, depending on the study, have either HFrEF or HFpEF (Fig. 5C), while patients in the dedicated renal outcomes studies have markedly different renal impairment, albuminuria and diabetes selection criteria between studies (Fig. 5B). This may explain differences seen in outcomes for CV death between some diabetes CVOTs and renal and HF studies. By contrast, HHF outcomes have consistently pointed to a benefit with SGLT2 inhibitors, regardless of the population characteristics. Continuing guideline updates can help clinicians to navigate the commonalities and distinguishing features among the complexity of evidence, such as the current recommendations to distinguish between ASCVD, CKD and HF settings when making treatment decisions in T2D.
To capture cardiorenal outcomes in the full breadth of patients encountered in clinical practice, we may need to look beyond clinical trials to real-world evidence studies, in order to confirm that CVOT findings are consistent in more diverse populations reflective of patients in the clinic . These studies can also help to establish health care resource utilisation benefits, and provide cost implications for the use of SGLT2 inhibitor and GLP-1 RA therapies in everyday practice . Early real-world evidence studies have already begun to confirm a consistent reduction of HHF with SGLT2 inhibitors, and ongoing studies are set to provide more comprehensive insights .
The paradigm shift that began with EMPA-REG OUTCOME and LEADER has led to SGLT2 inhibitors and GLP-1 RA being recognised not only in international diabetes guidelines, but also as an important consideration for patients with T2D in CVD prevention [28,29,30, 76, 77], HF [133,134,135] and CKD [41, 102] guidelines, where it has been suggested that these agents should be considered early in the course of diabetes management. These developments highlight the shift in treatment goals for T2D, from primarily focusing on the management of hyperglycaemia to a greater appreciation of the importance of managing cardiorenal risk, to reduce the high rates of CV deaths and cardiorenal hospitalisations in patients with T2D. However, SGLT2 inhibitors are not currently approved for primary prevention of cardiorenal comorbidities in T2D; additional evidence on outcomes in this setting may help us to explore the full potential of these agents.
Conclusions: saving lives with CVOTs
CVOTs designed to evaluate the CV safety of GLDs have highlighted clinical findings far greater than might have been originally expected. Providing a plethora of information on potentially unexpected outcomes, they have led to a paradigm shift that began with EMPA-REG OUTCOME and LEADER, and continued with subsequent CVOTs and now HF and renal outcomes studies [13, 60]. Despite the underlying mechanisms of such findings remaining a matter of theoretical postulation [60, 110,111,112, 124], the contribution of CVOTs as new evidence to the diabetes treatment armamentarium highlights a new era of standard treatment practices; endorsed by international guidelines such as ADA and EASD, to highlight the potential of SGLT2 inhibitors and GLP-1 RAs to improve cardiorenal outcomes for patients with T2D [38, 40]. In the post-CVOT era, people living with T2D are now able to benefit from treatments that can provide a therapeutic effect across the cardio-renal metabolic axis of T2D, while their physicians have options to achieve clinically meaningful reductions in CV, HF and renal outcomes, and even to reduce mortality (Fig. 6).
Availability of data and materials
Not applicable—new data or materials were used for this manuscript.
American College of Cardiology
American Diabetes Association
Atherosclerotic cardiovascular disease
Body mass index
Cardiovascular outcomes trial
European Association for the Study of Diabetes
European Dialysis and Transplant Association
Estimated glomerular filtration rate
European Renal Association
Europe Society of Cardiology
End-stage renal disease
European Renal and Cardiovascular Medicine
U.S. Food and Drug Administration
- GLP-1 RA:
Glucagon-like peptide-1 receptor agonist
Heart failure with preserved ejection fraction
Heart failure with reduced ejection fraction
Hospitalisation for heart failure
Kidney Disease Improving Global Outcomes
Major adverse cardiovascular events
Relative risk reduction
Sodium–glucose transporter 2
Type 2 diabetes
Thrombolysis In Myocardial Infarction
3-Point major adverse cardiovascular events
4-Point major adverse cardiovascular events
Cho NH, Shaw JE, Karuranga S, Huang Y, da Rocha Fernandes JD, Ohlrogge AW, et al. IDF Diabetes Atlas: global estimates of diabetes prevalence for 2017 and projections for 2045. Diabetes Res Clin Pract. 2018;138:271–81.
Nwaneri C, Cooper H, Bowen-Jones D. Mortality in type 2 diabetes mellitus: magnitude of the evidence from a systematic review and meta-analysis. Br J Diabetes Vasc Dis. 2013;13:192–207.
Almourani R, Chinnakotla B, Patel R, Kurukulasuriya LR, Sowers J. Diabetes and cardiovascular disease: an update. Curr Diabetes Rep. 2019;19:161.
Einarson TR, Acs A, Ludwig C, Panton UH. Prevalence of cardiovascular disease in type 2 diabetes: a systematic literature review of scientific evidence from across the world in 2007–2017. Cardiovasc Diabetol. 2018;17:83.
Shah AD, Langenberg C, Rapsomaniki E, Denaxas S, Pujades-Rodriguez M, Gale CP, et al. Type 2 diabetes and incidence of cardiovascular diseases: a cohort study in 1·9 million people. Lancet Diabetes Endocrinol. 2015;3:105–13.
Dauriz M, Mantovani A, Bonapace S, Verlato G, Zoppini G, Bonora E, et al. Prognostic impact of diabetes on long-term survival outcomes in patients with heart failure: a meta-analysis. Diabetes Care. 2017;40:1597–605.
Davis TME, Coleman RL, Holman RR, UKPDS Group. Prognostic significance of silent myocardial infarction in newly diagnosed type 2 diabetes mellitus: United Kingdom Prospective Diabetes Study (UKPDS) 79. Circulation. 2013;127:980–7.
White JR. A brief history of the development of diabetes medications. Diabetes Spectr. 2014;27:82–6.
Griffin SJ, Leaver JK, Irving GJ. Impact of metformin on cardiovascular disease: a meta-analysis of randomised trials among people with type 2 diabetes. Diabetologia. 2017;60:1620–9.
Hinnen D, Kruger DF. Cardiovascular risks in type 2 diabetes and the interpretation of cardiovascular outcome trials. Diabetes Metab Syndr Obes Targets Ther. 2019;12:447–55.
American Diabetes Association. Implications of the United Kingdom prospective diabetes study. Diabetes Care. 2002;25(Supplement 1):S28-32.
Udell JA, Cavender MA, Bhatt DL, Chatterjee S, Farkouh ME, Scirica BM. Glucose-lowering drugs or strategies and cardiovascular outcomes in patients with or at risk for type 2 diabetes: a meta-analysis of randomised controlled trials. Lancet Diabetes Endocrinol. 2015;3:356–66.
Schernthaner G, Drexel H, Moshkovich E, Zilaitiene B, Martinka E, Czupryniak L, et al. SGLT2 inhibitors in T2D and associated comorbidities—differentiating within the class. BMC Endocr Disord. 2019;19:64.
Schernthaner G, Wanner C, Jurišić-Eržen D, Guja C, Gumprecht J, Jarek-Martynowa IR, et al. CARMELINA: an important piece of the DPP-4 inhibitor CVOT puzzle. Diabetes Res Clin Pract. 2019;153:30–40.
Husain M, Birkenfeld AL, Donsmark M, Dungan K, Eliaschewitz FG, Franco DR, et al. Oral semaglutide and cardiovascular outcomes in patients with type 2 diabetes. N Engl J Med. 2019;381:841–51.
Cannon CP, McGuire DK, Cherney DZI, Dagogo-Jack S, Pratley RE. Results of the eValuation of ERTugliflozin EffIcacy and Safety CardioVascular Outcomes Trial (VERTIS CV). In: p. Symposium.
Pratley RE. Implications of cardiovascular outcome trials with injectable antidiabetic agents. J Diabetes. 2018;10:801–3.
Bhatt DL, Szarek M, Steg PG, Cannon CP, Leiter LA, McGuire DK, et al. Sotagliflozin in patients with diabetes and recent worsening heart failure. N Engl J Med. 2021;384:117–28.
Bertsch T, McKeirnan K. ITCA 650. Clin Diabetes Publ Am Diabetes Assoc. 2018;36:265–7.
Rosenstock J, Perkovic V, Johansen OE, Cooper ME, Kahn SE, Marx N, et al. Effect of linagliptin vs placebo on major cardiovascular events in adults with type 2 diabetes and high cardiovascular and renal risk: The CARMELINA randomized clinical trial. JAMA. 2019;321:69–79.
Rosenstock J, Kahn SE, Johansen OE, Zinman B, Espeland MA, Woerle HJ, et al. Effect of linagliptin vs glimepiride on major adverse cardiovascular outcomes in patients with type 2 diabetes: The CAROLINA randomized clinical trial. JAMA. 2019;322:1155.
Green JB, Bethel MA, Armstrong PW, Buse JB, Engel SS, Garg J, et al. Effect of sitagliptin on cardiovascular outcomes in type 2 diabetes. N Engl J Med. 2015;373:232–42.
Gerstein HC, Sattar N, Rosenstock J, Ramasundarahettige C, Pratley R, Lopes RD, et al. Cardiovascular and renal outcomes with efpeglenatide in type 2 diabetes. N Engl J Med. 2021;385:896–907.
Ruff CT, Baron M, Im K, O’Donoghue ML, Fiedorek FT, Sabatine MS. Subcutaneous infusion of exenatide and cardiovascular outcomes in type 2 diabetes: a non-inferiority randomized controlled trial. Nat Med. 2022;28:89–95.
Regier EE, Venkat MV, Close KL. More than 7 years of hindsight: revisiting the FDA’s 2008 guidance on cardiovascular outcomes trials for type 2 diabetes medications. Clin Diabetes. 2016;34:173–80.
Pfeffer MA, Claggett B, Diaz R, Dickstein K, Gerstein HC, Køber LV, et al. Lixisenatide in patients with type 2 diabetes and acute coronary syndrome. N Engl J Med. 2015;373:2247–57.
Zinman B, Wanner C, Lachin JM, Fitchett D, Bluhmki E, Hantel S, et al. Empagliflozin, cardiovascular outcomes, and mortality in type 2 diabetes. N Engl J Med. 2015;373:2117–28.
Wanner C, Inzucchi SE, Lachin JM, Fitchett D, von Eynatten M, Mattheus M, et al. Empagliflozin and progression of kidney disease in type 2 diabetes. N Engl J Med. 2016;375:323–34.
Fitchett D, Zinman B, Wanner C, Lachin JM, Hantel S, Salsali A, et al. Heart failure outcomes with empagliflozin in patients with type 2 diabetes at high cardiovascular risk: results of the EMPA-REG OUTCOME® trial. Eur Heart J. 2016;37:1526–34.
Neal B, Perkovic V, Mahaffey KW, de Zeeuw D, Fulcher G, Erondu N, et al. Canagliflozin and cardiovascular and renal events in type 2 diabetes. N Engl J Med. 2017;377:644–57.
Marso SP, Bain SC, Consoli A, Eliaschewitz FG, Jódar E, Leiter LA, et al. Semaglutide and cardiovascular outcomes in patients with type 2 diabetes. N Engl J Med. 2016;375:1834–44.
Marso SP, Daniels GH, Brown-Frandsen K, Kristensen P, Mann JFE, Nauck MA, et al. Liraglutide and cardiovascular outcomes in type 2 diabetes. N Engl J Med. 2016;375:311–22.
Holman RR, Bethel MA, Mentz RJ, Thompson VP, Lokhnygina Y, Buse JB, et al. Effects of once-weekly exenatide on cardiovascular outcomes in type 2 diabetes. N Engl J Med. 2017;377:1228–39.
Gerstein HC, Colhoun HM, Dagenais GR, Diaz R, Lakshmanan M, Pais P, et al. Dulaglutide and cardiovascular outcomes in type 2 diabetes (REWIND): a double-blind, randomised placebo-controlled trial. Lancet Lond Engl. 2019;394:121–30.
Hernandez AF, Green JB, Janmohamed S, D’Agostino RB, Granger CB, Jones NP, et al. Albiglutide and cardiovascular outcomes in patients with type 2 diabetes and cardiovascular disease (Harmony Outcomes): a double-blind, randomised placebo-controlled trial. Lancet Lond Engl. 2018;392:1519–29.
Perkovic V, Jardine MJ, Neal B, Bompoint S, Heerspink HJL, Charytan DM, et al. Canagliflozin and renal outcomes in type 2 diabetes and nephropathy. N Engl J Med. 2019;380:2295–306.
Wiviott SD, Raz I, Bonaca MP, Mosenzon O, Kato ET, Cahn A, et al. Dapagliflozin and cardiovascular outcomes in type 2 diabetes. N Engl J Med. 2019;380:347–57.
Cosentino F, Grant PJ, Aboyans V, Bailey CJ, Ceriello A, Delgado V, et al. 2019 ESC guidelines on diabetes, pre-diabetes, and cardiovascular diseases developed in collaboration with the EASD. Eur Heart J. 2020;41:255–323.
Das SR, Everett BM, Birtcher KK, Brown JM, Cefalu WT, Januzzi JL, et al. 2018 ACC Expert consensus decision pathway on novel therapies for cardiovascular risk reduction in patients with type 2 diabetes and atherosclerotic cardiovascular disease. J Am Coll Cardiol. 2018;72:3200–23.
Davies MJ, D’Alessio DA, Fradkin J, Kernan WN, Mathieu C, Mingrone G, et al. Management of hyperglycaemia in type 2 diabetes, 2018. A consensus report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD). Diabetologia. 2018;2018(61):2461–98.
Kidney Disease: Improving Global Outcomes (KDIGO) Diabetes Work Group. KDIGO 2020 clinical practice guideline for diabetes management in chronic kidney disease. Kidney Int. 2020;98:S1-115.
Buse JB, Wexler DJ, Tsapas A, Rossing P, Mingrone G, Mathieu C, et al. 2019 update to: Management of hyperglycaemia in type 2 diabetes, 2018. A consensus report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD). Diabetologia. 2020;63:221–8.
Das SR, Everett BM, Birtcher KK, Brown JM, Januzzi JL, Kalyani RR, et al. 2020 Expert consensus decision pathway on novel therapies for cardiovascular risk reduction in patients with type 2 diabetes. J Am Coll Cardiol. 2020;76:1117–45.
American Diabetes Association Professional Practice Committee. 9. Pharmacologic approaches to glycemic treatment: Standards of Medical Care in Diabetes—2022. Diabetes Care. 2022;45 Supplement_1:S125–43.
Chrysant SG. Stopping the cardiovascular disease continuum: focus on prevention. World J Cardiol. 2010;2:43.
Lam CSP, Ferreira JP, Pfarr E, Sim D, Tsutsui H, Anker SD, et al. Regional and ethnic influences on the response to empagliflozin in patients with heart failure and a reduced ejection fraction: the EMPEROR-Reduced trial. Eur Heart J. 2021;42:4442–51.
Nielsen HK, DeChiaro S, Goldman B. Evaluation of consistency of treatment response across regions—the LEADER trial in relation to the ICH E17 guideline. Front Med. 2021;8:662775.
Schernthaner G, Lotan C, Baltadzhieva-Trendafilova E, Ceponis J, Clodi M, Ducena K, et al. Unrecognised cardiovascular disease in type 2 diabetes: is it time to act earlier? Cardiovasc Diabetol. 2018;17:145.
Fitchett D, Inzucchi SE, Cannon CP, McGuire DK, Scirica BM, Johansen OE, et al. Empagliflozin reduced mortality and hospitalization for heart failure across the spectrum of cardiovascular risk in the EMPA-REG OUTCOME trial. Circulation. 2019;139:1384–95.
Verma S, Mazer CD, Fitchett D, Inzucchi SE, Pfarr E, George JT, et al. Empagliflozin reduces cardiovascular events, mortality and renal events in participants with type 2 diabetes after coronary artery bypass graft surgery: subanalysis of the EMPA-REG OUTCOME® randomised trial. Diabetologia. 2018;61:1712–23.
Verma S, Mazer CD, Bhatt DL, Raj SR, Yan AT, Verma A, et al. Empagliflozin and cardiovascular outcomes in patients with type 2 diabetes and left ventricular hypertrophy: a subanalysis of the EMPA-REG OUTCOME trial. Diabetes Care. 2019;42:e42–4.
Verma S, Mazer CD, Al-Omran M, Inzucchi SE, Fitchett D, Hehnke U, et al. Cardiovascular outcomes and safety of empagliflozin in patients with type 2 diabetes mellitus and peripheral artery disease: a subanalysis of EMPA-REG OUTCOME. Circulation. 2018;137:405–7.
Böhm M, Slawik J, Brueckmann M, Mattheus M, George JT, Ofstad AP, et al. Efficacy of empagliflozin on heart failure and renal outcomes in patients with atrial fibrillation: data from the EMPA-REG OUTCOME trial. Eur J Heart Fail. 2020;22:126–35.
Neuen BL, Ohkuma T, Neal B, Matthews DR, de Zeeuw D, Mahaffey KW, et al. Effect of canagliflozin on renal and cardiovascular outcomes across different levels of albuminuria: data from the CANVAS Program. J Am Soc Nephrol. 2019;30:2229–42.
Yu J, Arnott C, Neuen BL, Heersprink HL, Mahaffey KW, Cannon CP, et al. Cardiovascular and renal outcomes with canagliflozin according to baseline diuretic use: a post hoc analysis from the CANVAS Program. ESC Heart Fail. 2021;8:1482–93.
Scheen AJ. Cardiovascular effects of gliptins. Nat Rev Cardiol. 2013;10:73–84.
Scirica BM, Bhatt DL, Braunwald E, Steg PG, Davidson J, Hirshberg B, et al. Saxagliptin and cardiovascular outcomes in patients with type 2 diabetes mellitus. N Engl J Med. 2013;369:1317–26.
White WB, Cannon CP, Heller SR, Nissen SE, Bergenstal RM, Bakris GL, et al. Alogliptin after acute coronary syndrome in patients with type 2 diabetes. N Engl J Med. 2013;369:1327–35.
Rosano G, Seferović P. Hypoglycaemic agents in patients with heart failure. Int Cardiovasc Forum J. 2019. https://doi.org/10.17987/icfj.v18i0.623.
Nagahisa T, Saisho Y. Cardiorenal protection: potential of SGLT2 inhibitors and GLP-1 receptor agonists in the treatment of type 2 diabetes. Diabetes Ther Res Treat Educ Diabetes Relat Disord. 2019;10:1733–52.
Giugliano D, Longo M, Scappaticcio L, Bellastella G, Maiorino MI, Esposito K. SGLT-2 inhibitors and cardiorenal outcomes in patients with or without type 2 diabetes: a meta-analysis of 11 CVOTs. Cardiovasc Diabetol. 2021;20:236.
Zelniker TA, Wiviott SD, Raz I, Im K, Goodrich EL, Bonaca MP, et al. SGLT2 inhibitors for primary and secondary prevention of cardiovascular and renal outcomes in type 2 diabetes: a systematic review and meta-analysis of cardiovascular outcome trials. Lancet Lond Engl. 2019;393:31–9.
Wheeler DC, Stefánsson BV, Jongs N, Chertow GM, Greene T, Hou FF, et al. Effects of dapagliflozin on major adverse kidney and cardiovascular events in patients with diabetic and non-diabetic chronic kidney disease: a prespecified analysis from the DAPA-CKD trial. Lancet Diabetes Endocrinol. 2021;9:22–31.
Petrie MC, Verma S, Docherty KF, Inzucchi SE, Anand I, Belohlávek J, et al. Effect of dapagliflozin on worsening heart failure and cardiovascular death in patients with heart failure with and without diabetes. JAMA. 2020;323:1353–68.
Giugliano D, Scappaticcio L, Longo M, Caruso P, Maiorino MI, Bellastella G, et al. GLP-1 receptor agonists and cardiorenal outcomes in type 2 diabetes: an updated meta-analysis of eight CVOTs. Cardiovasc Diabetol. 2021;20:189.
Mountfort K. ADA 2019 Oral Semaglutide—The PIONEER Program Trials. https://www.touchendocrinology.com/insight/ada-2019-oral-semaglutide-the-pioneer-program-trials/. Accessed 17 Aug 2021.
Aroda VR. A review of GLP-1 receptor agonists: evolution and advancement, through the lens of randomised controlled trials. Diabetes Obes Metab. 2018;20(Suppl 1):22–33.
Heerspink HJL, Stefánsson BV, Correa-Rotter R, Chertow GM, Greene T, Hou F-F, et al. Dapagliflozin in patients with chronic kidney disease. N Engl J Med. 2020;383:1436–46.
McMurray JJV, Solomon SD, Inzucchi SE, Køber L, Kosiborod MN, Martinez FA, et al. Dapagliflozin in patients with heart failure and reduced ejection fraction. N Engl J Med. 2019;381:1995–2008.
Anker SD, Butler J, Filippatos G, Khan MS, Marx N, Lam CSP, et al. Effect of empagliflozin on cardiovascular and renal outcomes in patients with heart failure by baseline diabetes status: results from the EMPEROR-Reduced trial. Circulation. 2021;143:337–49.
Packer M, Anker SD, Butler J, Filippatos G, Pocock SJ, Carson P, et al. Cardiovascular and renal outcomes with empagliflozin in heart failure. N Engl J Med. 2020;383:1413–24.
Bhatt DL, Szarek M, Pitt B, Cannon CP, Leiter LA, McGuire DK, et al. Sotagliflozin in patients with diabetes and chronic kidney disease. N Engl J Med. 2021;384:129–39.
Schernthaner G, Karasik A, Abraitienė A, Ametov AS, Gaàl Z, Gumprecht J, et al. Evidence from routine clinical practice: EMPRISE provides a new perspective on CVOTs. Cardiovasc Diabetol. 2019;18:115.
Patorno E, Pawar A, Franklin JM, Najafzadeh M, Déruaz-Luyet A, Brodovicz KG, et al. Empagliflozin and the risk of heart failure hospitalization in routine clinical care. Circulation. 2019;139:2822–30.
Pasternak B, Wintzell V, Melbye M, Eliasson B, Svensson A-M, Franzén S, et al. Use of sodium-glucose co-transporter 2 inhibitors and risk of serious renal events: Scandinavian cohort study. BMJ. 2020;369:m1186.
Heerspink HJL, Karasik A, Thuresson M, Melzer-Cohen C, Chodick G, Khunti K, et al. Kidney outcomes associated with use of SGLT2 inhibitors in real-world clinical practice (CVD-REAL 3): a multinational observational cohort study. Lancet Diabetes Endocrinol. 2020;8:27–35.
Filion KB, Lix LM, Yu OH, Dell’Aniello S, Douros A, Shah BR, et al. Sodium glucose cotransporter 2 inhibitors and risk of major adverse cardiovascular events: multi-database retrospective cohort study. BMJ. 2020;370:m3342.
Idris I, Zhang R, Mamza JB, Ford M, Morris T, Banerjee A, et al. Lower risk of hospitalisation for heart failure, kidney disease and death with sodium glucose co-transporter-2 compared to dipeptidyl peptidase-4 inhibitors in type 2 diabetes regardless of prior cardiovascular or kidney disease: a retrospective cohort study in UK primary care. Diabetes Obes Metab. 2021;23:2207–14.
Lam CSP, Karasik A, Melzer-Cohen C, Cavender MA, Kohsaka S, Norhammar A, et al. Association of sodium-glucose cotransporter-2 inhibitors with outcomes in type 2 diabetes with reduced and preserved left ventricular ejection fraction: analysis from the CVD-REAL 2 study. Diabetes Obes Metab. 2021;23:1431–5.
Cavender MA, Norhammar A, Birkeland KI, Jørgensen ME, Wilding JP, Khunti K, et al. SGLT-2 inhibitors and cardiovascular risk: an analysis of CVD-REAL. J Am Coll Cardiol. 2018;71:2497–506.
Udell JA, Yuan Z, Rush T, Sicignano NM, Galitz M, Rosenthal N. Cardiovascular outcomes and risks after initiation of a sodium glucose cotransporter 2 inhibitor: results from the EASEL population-based cohort study (evidence for cardiovascular outcomes with sodium glucose cotransporter 2 inhibitors in the real world). Circulation. 2018;137:1450–9.
Udell JA, Yuan Z, Ryan P, Rush T, Sicignano NM, Galitz M, et al. Cardiovascular outcomes and mortality after initiation of canagliflozin: analyses from the EASEL Study. Endocrinol Diabetes Metab. 2020;3:e00096.
AstraZeneca. Forxiga approved in the EU for heart failure. https://www.astrazeneca.com/media-centre/press-releases/2020/forxiga-approved-in-the-eu-for-heart-failure.html. Accessed 14 Sept 2021.
Boehringer Ingelheim. Jardiance® (empagliflozin) approved in Europe for the treatment of heart failure with reduced ejection fraction. https://www.boehringer-ingelheim.com/press-release/reduced-heart-failure-treatment-approval-europe#:~:text=%20Jardiance%20%C2%AE%20%28empagliflozin%29%20approved%20in%20Europe%20for,with%20insufficiently%20controlled%20type%202%20diabetes...%20More%20. Accessed 14 Sept 2021.
Boehringer Ingelheim. Breakthrough results for empagliflozin confirm EMPEROR-Preserved as first and only successful trial for heart failure with preserved ejection fraction. https://www.boehringer-ingelheim.com/press-release/emperor-preserved-heart-failure-toplineresults. Accessed 17 Aug 2021.
Anker SD, Butler J, Filippatos G, Ferreira JP, Bocchi E, Böhm M, et al. Empagliflozin in heart failure with a preserved ejection fraction. N Engl J Med. 2021;385:1451–61.
Drazner MH. SGLT2 inhibition in heart failure with a preserved ejection fraction—a win against a formidable foe. N Engl J Med. 2021;385:1451–61.
Zannad F, Ferreira JP, Pocock SJ, Anker SD, Butler J, Filippatos G, et al. SGLT2 inhibitors in patients with heart failure with reduced ejection fraction: a meta-analysis of the EMPEROR-Reduced and DAPA-HF trials. Lancet Lond Engl. 2020;396:819–29.
Kosiborod M, Cavender MA, Fu AZ, Wilding JP, Khunti K, Holl RW, et al. Lower risk of heart failure and death in patients initiated on sodium-glucose cotransporter-2 inhibitors versus other glucose-lowering drugs: The CVD-REAL study (comparative effectiveness of cardiovascular outcomes in new users of sodium-glucose cotransporter-2 inhibitors). Circulation. 2017;136:249–59.
Kosiborod M, Lam CSP, Kohsaka S, Kim DJ, Karasik A, Shaw J, et al. Cardiovascular events associated with SGLT-2 inhibitors versus other glucose-lowering drugs: the CVD-REAL 2 study. J Am Coll Cardiol. 2018;71:2628–39.
Taylor P. AZ gets European approvals for Forxiga in chronic kidney disease. https://pharmaphorum.com/news/az-gets-european-approvals-for-forxiga-in-chronic-kidney-disease. Accessed 17 Aug 2021.
Perkovic V, de Zeeuw D, Mahaffey KW, Fulcher G, Erondu N, Shaw W, et al. Canagliflozin and renal outcomes in type 2 diabetes: results from the CANVAS Program randomised clinical trials. Lancet Diabetes Endocrinol. 2018;6:691–704.
On behalf of the VERTIS CV Investigators, Cherney DZI, Charbonnel B, Cosentino F, Dagogo-Jack S, McGuire DK, et al. Effects of ertugliflozin on kidney composite outcomes, renal function and albuminuria in patients with type 2 diabetes mellitus: an analysis from the randomised VERTIS CV trial. Diabetologia. 2021;64:1256–67.
Cherney DZI, Cosentino F, Dagogo-Jack S, McGuire DK, Pratley R, Frederich R, et al. Ertugliflozin and slope of chronic eGFR: prespecified analyses from the randomized VERTIS CV trial. Clin J Am Soc Nephrol. 2021;16:1345–54.
Raz I, Wiviott SD, Yanuv I, Rozenberg A, Zelniker TA, Cahn A, et al. 244-OR: Effects of dapagliflozin on the urinary albumin-to-creatinine ratio in patients with type 2 diabetes: a predefined analysis from the DECLARE-TIMI 58 randomised, placebo-controlled trial. Diabetes. 2019;68(Supplement 1):244-OR.
Mann JFE, Ørsted DD, Brown-Frandsen K, Marso SP, Poulter NR, Rasmussen S, et al. Liraglutide and renal outcomes in type 2 diabetes. N Engl J Med. 2017;377:839–48.
Gerstein HC, Colhoun HM, Dagenais GR, Diaz R, Lakshmanan M, Pais P, et al. Dulaglutide and renal outcomes in type 2 diabetes: an exploratory analysis of the REWIND randomised, placebo-controlled trial. Lancet. 2019;394:131–8.
Sakai Y, Suzuki A, Mugishima K, Sumi Y, Otsuka Y, Otsuka T, et al. Effects of alogliptin in chronic kidney disease patients with type 2 diabetes. Intern Med. 2014;53:195–203.
Cornel JH, Bakris GL, Stevens SR, Alvarsson M, Bax WA, Chuang L-M, et al. Effect of sitagliptin on kidney function and respective cardiovascular outcomes in type 2 diabetes: outcomes from TECOS. Diabetes Care. 2016;39:2304–10.
Mosenzon O, Leibowitz G, Bhatt DL, Cahn A, Hirshberg B, Wei C, et al. Effect of Saxagliptin on renal outcomes in the SAVOR-TIMI 53 trial. Diabetes Care. 2017;40:69–76.
Rosenstock J, Perkovic V, Alexander JH, Cooper ME, Marx N, Pencina MJ, et al. Rationale, design, and baseline characteristics of the CArdiovascular safety and Renal Microvascular outcomE study with LINAgliptin (CARMELINA®): a randomized, double-blind, placebo-controlled clinical trial in patients with type 2 diabetes and high cardio-renal risk. Cardiovasc Diabetol. 2018;17:39.
Sarafidis P, Ferro CJ, Morales E, Ortiz A, Malyszko J, Hojs R, et al. SGLT-2 inhibitors and GLP-1 receptor agonists for nephroprotection and cardioprotection in patients with diabetes mellitus and chronic kidney disease. A consensus statement by the EURECA-m and the DIABESITY working groups of the ERA-EDTA. Nephrol Dial Transplant. 2019;34:208–30.
Brown E, Heerspink HJL, Cuthbertson DJ, Wilding JPH. SGLT2 inhibitors and GLP-1 receptor agonists: established and emerging indications. Lancet. 2021;398:262–76.
Schernthaner G, Shehadeh N, Ametov AS, Bazarova AV, Ebrahimi F, Fasching P, et al. Worldwide inertia to the use of cardiorenal protective glucose-lowering drugs (SGLT2i and GLP-1 RA) in high-risk patients with type 2 diabetes. Cardiovasc Diabetol. 2020;19:185.
Piepoli MF, Hoes AW, Agewall S, Albus C, Brotons C, Catapano AL, et al. 2016 European Guidelines on cardiovascular disease prevention in clinical practice: The Sixth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of 10 societies and by invited experts)Developed with the special contribution of the European Association for Cardiovascular Prevention & Rehabilitation (EACPR). Eur Heart J. 2016;37:2315–81.
Hong D, Si L, Jiang M, Shao H, Ming W, Zhao Y, et al. Cost effectiveness of sodium-glucose cotransporter-2 (SGLT2) inhibitors, glucagon-like peptide-1 (GLP-1) receptor agonists, and dipeptidyl peptidase-4 (DPP-4) inhibitors: a systematic review. Pharmacoeconomics. 2019;37:777–818.
Hung A, Jois B, Lugo A, Slejko JF. Cost-effectiveness of diabetes treatment sequences to inform step therapy policies. Am J Manag Care. 2020;26:e76-83.
Arnott C, Neuen BL, Heerspink HJL, Figtree GA, Kosiborod M, Lam CS, et al. The effects of combination canagliflozin and glucagon-like peptide-1 receptor agonist therapy on intermediate markers of cardiovascular risk in the CANVAS program. Int J Cardiol. 2020;318:126–9.
Goncalves E, Bell DSH. Combination treatment of SGLT2 Inhibitors and GLP-1 receptor agonists: symbiotic effects on metabolism and cardiorenal risk. Diabetes Ther. 2018;9:919–26.
Hallow KM, Greasley PJ, Helmlinger G, Chu L, Heerspink HJ, Boulton DW. Evaluation of renal and cardiovascular protection mechanisms of SGLT2 inhibitors: model-based analysis of clinical data. Am J Physiol Renal Physiol. 2018;315:F1295–306.
Packer M. SGLT2 inhibitors produce cardiorenal benefits by promoting adaptive cellular reprogramming to induce a state of fasting mimicry: a paradigm shift in understanding their mechanism of action. Diabetes Care. 2020;43:508–11.
Sloan LA. Review of glucagon-like peptide-1 receptor agonists for the treatment of type 2 diabetes mellitus in patients with chronic kidney disease and their renal effects. J Diabetes. 2019;11:938–48.
Inzucchi SE, Kosiborod M, Fitchett D, Wanner C, Hehnke U, Kaspers S, et al. Improvement in cardiovascular outcomes with empagliflozin is independent of glycemic control. Circulation. 2018;138:1904–7.
Cooper ME, Inzucchi SE, Zinman B, Hantel S, von Eynatten M, Wanner C, et al. Glucose control and the effect of empagliflozin on kidney outcomes in type 2 diabetes: an analysis from the EMPA-REG OUTCOME trial. Am J Kidney Dis. 2019;74:713–5.
The LEADER Publication Committee on behalf of the LEADER Trial Investigators, Zinman B, Nauck MA, Bosch-Traberg H, Frimer-Larsen H, Ørsted DD, et al. Liraglutide and glycaemic outcomes in the LEADER trial. Diabetes Ther. 2018;9:2383–92.
Cefalu WT, Kaul S, Gerstein HC, Holman RR, Zinman B, Skyler JS, et al. Cardiovascular outcomes trials in type 2 diabetes: where do we go from here? Reflections from a Diabetes Care Editors’ Expert Forum. Diabetes Care. 2018;41:14–31.
Avogaro A, Fadini GP, Del Prato S. Reinterpreting cardiorenal protection of renal sodium-glucose cotransporter 2 inhibitors via cellular life history programming. Diabetes Care. 2020;43:501–7.
Ferrannini E, Mark M, Mayoux E. CV protection in the EMPA-REG OUTCOME trial: a “thrifty substrate” hypothesis. Diabetes Care. 2016;39:1108–14.
Mudaliar S, Alloju S, Henry RR. Can a shift in fuel energetics explain the beneficial cardiorenal outcomes in the EMPA-REG OUTCOME study? A unifying hypothesis. Diabetes Care. 2016;39:1115–22.
Hallow KM, Helmlinger G, Greasley PJ, McMurray JJV, Boulton DW. Why do SGLT2 inhibitors reduce heart failure hospitalization? A differential volume regulation hypothesis. Diabetes Obes Metab. 2018;20:479–87.
Lopaschuk GD, Verma S. Mechanisms of cardiovascular benefits of sodium glucose co-transporter 2 (SGLT2) inhibitors. JACC Basic Transl Sci. 2020;5:632–44.
Uthman L, Baartscheer A, Bleijlevens B, Schumacher CA, Fiolet JWT, Koeman A, et al. Class effects of SGLT2 inhibitors in mouse cardiomyocytes and hearts: inhibition of Na+/H+ exchanger, lowering of cytosolic Na+ and vasodilation. Diabetologia. 2018;61:722–6.
Yaribeygi H, Butler AE, Atkin SL, Katsiki N, Sahebkar A. Sodium-glucose cotransporter 2 inhibitors and inflammation in chronic kidney disease: Possible molecular pathways. J Cell Physiol. 2018;234:223–30.
Sposito AC, Berwanger O, de Carvalho LSF, Saraiva JFK. GLP-1RAs in type 2 diabetes: mechanisms that underlie cardiovascular effects and overview of cardiovascular outcome data. Cardiovasc Diabetol. 2018;17:157.
Mosenzon O, Wiviott SD, Cahn A, Rozenberg A, Yanuv I, Goodrich EL, et al. Effects of dapagliflozin on development and progression of kidney disease in patients with type 2 diabetes: an analysis from the DECLARE-TIMI 58 randomised trial. Lancet Diabetes Endocrinol. 2019;7:606–17.
Wanner C, Lachin JM, Inzucchi SE, Fitchett D, Mattheus M, George J, et al. Empagliflozin and clinical outcomes in patients with type 2 diabetes mellitus, established cardiovascular disease, and chronic kidney disease. Circulation. 2018;137:119–29.
Herrington WG, Preiss D, Haynes R, von Eynatten M, Staplin N, Hauske SJ, et al. The potential for improving cardio-renal outcomes by sodium-glucose co-transporter-2 inhibition in people with chronic kidney disease: a rationale for the EMPA-KIDNEY study. Clin Kidney J. 2018;11:749–61.
Kjeldsen SE, von Lueder TG, Smiseth OA, Wachtell K, Mistry N, Westheim AS, et al. Medical therapies for heart failure with preserved ejection fraction. Hypertens Dallas Tex. 1979;75:23–32.
Packer M, Butler J, Zannad F, Filippatos G, Ferreira JP, Pocock SJ, et al. Effect of empagliflozin on worsening heart failure events in patients with heart failure and a preserved ejection fraction: the EMPEROR-Preserved trial. Circulation. 2021;144:1284–94.
Packer M, Zannad F, Butler J, Filippatos G, Ferreira JP, Pocock SJ, et al. Influence of endpoint definitions on the effect of empagliflozin on major renal outcomes in the EMPEROR-Preserved trial. Eur J Heart Fail. 2021;23:1798–9.
Packer M, Butler J, Zannad F, Pocock SJ, Filippatos G, Ferreira JP, et al. Empagliflozin and major renal outcomes in heart failure. N Engl J Med. 2021;385:1531–3.
Ali A, Bain S, Hicks D, Newland Jones P, Patel DC, Evans M, et al. SGLT2 inhibitors: cardiovascular benefits beyond HbA1c-translating evidence into practice. Diabetes Ther Res Treat Educ Diabetes Relat Disord. 2019;10:1595–622.
Seferović PM, Fragasso G, Petrie M, Mullens W, Ferrari R, Thum T, et al. Heart failure association of the European Society of Cardiology: Update on sodium–glucose co-transporter 2 inhibitors in heart failure. Eur J Heart Fail. 2020;22:1984–6.
Seferović PM, Fragasso G, Petrie M, Mullens W, Ferrari R, Thum T, et al. Sodium–glucose co-transporter 2 inhibitors in heart failure: beyond glycaemic control. A position paper of the Heart Failure Association of the European Society of Cardiology. Eur J Heart Fail. 2020;22:1495–503.
Seferović PM, Coats AJS, Ponikowski P, Filippatos G, Huelsmann M, Jhund PS, et al. European Society of Cardiology/Heart Failure Association position paper on the role and safety of new glucose-lowering drugs in patients with heart failure. Eur J Heart Fail. 2020;22:196–213.
Hramiak I, Vilsbøll T, Gumprecht J, Silver R, Hansen T, Pettersson J, et al. Semaglutide treatment and renal function in the SUSTAIN 6 trial. Can J Diabetes. 2018;42:S42.
Tuttle K, Cherney D, Hadjadj S, Idorn T, Mosenzon O, Perkovic V, et al. MO051 Effects of semaglutide on chronic kidney disease outcomes: a post hoc pooled analysis from the SUSTAIN 6 and PIONEER 6 trials. Nephrol Dial Transplant. 2020;35(Supplement 3):gfaa140.MO051.
Leiter LA, Bain SC, Hramiak I, Jódar E, Madsbad S, Gondolf T, et al. Cardiovascular risk reduction with once-weekly semaglutide in subjects with type 2 diabetes: a post hoc analysis of gender, age, and baseline CV risk profile in the SUSTAIN 6 trial. Cardiovasc Diabetol. 2019;18:73.
Cannon CP, Pratley R, Dagogo-Jack S, Mancuso J, Huyck S, Masiukiewicz U, et al. Cardiovascular outcomes with ertugliflozin in type 2 diabetes. N Engl J Med. 2020;383:1425–35.
McMurray JJV, Wheeler DC, Stefánsson BV, Jongs N, Postmus D, Correa-Rotter R, et al. Effect of dapagliflozin on clinical outcomes in patients with chronic kidney disease, with and without cardiovascular disease. Circulation. 2021;143:438–48.
Neuen BL, Ohkuma T, Neal B, Matthews DR, de Zeeuw D, Mahaffey KW, et al. Cardiovascular and renal outcomes with canagliflozin according to baseline kidney function. Circulation. 2018;138:1537–50.
Cannon CP, McGuire DK, Pratley R, Dagogo-Jack S, Mancuso J, Huyck S, et al. Design and baseline characteristics of the eValuation of ERTugliflozin effIcacy and Safety CardioVascular outcomes trial (VERTIS-CV). Am Heart J. 2018;206:11–23.
Keech A, Colquhoun D, Best J, Kirby A, Simes RJ, Hunt D, et al. Secondary prevention of cardiovascular events with long-term pravastatin in patients with diabetes or impaired fasting glucose: results from the LIPID trial. Diabetes Care. 2003;26:2713–21.
Costa J, Borges M, David C, Vaz CA. Efficacy of lipid lowering drug treatment for diabetic and non-diabetic patients: meta-analysis of randomised controlled trials. BMJ. 2006;332:1115–24.
Ludwig L, Darmon P, Guerci B. Computing and interpreting the number needed to treat for cardiovascular outcomes trials: perspective on GLP-1 RA and SGLT-2i therapies. Cardiovasc Diabetol. 2020;19:65.
Newman DH. Aspirin to prevent cardiovascular disease in patients with known heart disease or strokes. https://www.thennt.com/nnt/aspirin-for-cardiovascular-prevention-after-prior-heart-attack-or-stroke/. Accessed 1 Mar 2022.
Huang ES, Meigs JB, Singer DE. The effect of interventions to prevent cardiovascular disease in patients with type 2 diabetes mellitus. Am J Med. 2001;111:633–42.
Williams DM, Evans M. Dapagliflozin for heart failure with preserved ejection fraction: will the DELIVER study deliver? Diabetes Ther Res Treat Educ Diabetes Relat Disord. 2020;11:2207–19.
Anker SD, Butler J, Filippatos GS, Jamal W, Salsali A, Schnee J, et al. Evaluation of the effects of sodium-glucose co-transporter 2 inhibition with empagliflozin on morbidity and mortality in patients with chronic heart failure and a preserved ejection fraction: rationale for and design of the EMPEROR-Preserved trial. Eur J Heart Fail. 2019;21:1279–87.
Rhee JJ, Jardine MJ, Chertow GM, Mahaffey KW. Dedicated kidney disease-focused outcome trials with sodium-glucose cotransporter-2 inhibitors: lessons from CREDENCE and expectations from DAPA-HF, DAPA-CKD, and EMPA-KIDNEY. Diabetes Obes Metab. 2020;22(Suppl 1):46–54.
Anker SD, Butler J, Filippatos G, Shahzeb Khan M, Ferreira JP, Bocchi E, et al. Baseline characteristics of patients with heart failure with preserved ejection fraction in the EMPEROR-Preserved trial. Eur J Heart Fail. 2020;22:2383–92.
Qureshi WT, Zhang Z-M, Chang PP, Rosamond WD, Kitzman DW, Wagenknecht LE, et al. Silent myocardial infarction and long-term risk of heart failure. J Am Coll Cardiol. 2018;71:1–8.
Yoneyama K, Venkatesh BA, Wu CO, Mewton N, Gjesdal O, Kishi S, et al. Diabetes mellitus and insulin resistance associate with left ventricular shape and torsion by cardiovascular magnetic resonance imaging in asymptomatic individuals from the multi-ethnic study of atherosclerosis. J Cardiovasc Magn Reson. 2018;20:53.
Editorial support was provided by Fortis Pharma Communications, with financial support by Boehringer Ingelheim (BI). The opinions expressed are entirely the authors’ own and the only involvement of BI was to have sight of the manuscript for accuracy and support with the initial literature search from Lucie Hosch, an employee of BI.
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MJD reported board membership and consultancy fees from Novo Nordisk, Sanofi-Aventis, Lilly, Merck, Sharp & Dohme, Boehringer Ingelheim, AstraZeneca, Servier, and Janssen. MJD reported institutional grants from Novo Nordisk, Sanofi-Aventis, Lilly, Boehringer Ingelheim and Janssen. MJD reported payment for lectures or speaker bureaus from Novo Nordisk, Sanofi-Aventis, Lilly, Merck, Sharp & Dohme, Boehringer Ingelheim, AstraZeneca, Janssen, Mitsubishi Tanabe Pharma, and Takeda Pharmaceuticals International.
HD declares no conflicts of interest.
FRJ has received consulting honoraria from Boehringer Ingelheim, Mundipharma, Astra Zeneca, Novo Nordisk, MSD, Lilly, and Sanofi.DKM has had leadership roles in clinical trials for AstraZeneca, Boehringer Ingelheim, Eisai, Esperion, GlaxoSmithKline, Janssen, Lexicon, Merck & Co., Inc., Novo Nordisk, CSL Behring, and Sanofi USA; and has received consultancy fees from AstraZeneca, Boehringer Ingelheim, Lilly USA, Merck & Co., Inc., Pfizer, Novo Nordisk, Metavant, Afimmune, and Sanofi.
ZP has received consulting honoraria from Boehringer Ingelheim, Novo Nordisk, and Sanofi.
PMS has received honorarium for lectures for Medtronic, Abbott, Servier, Astra Zeneca, and Respicardia; Boehringer Ingelheim consultancy agreement and honorarium for lecture, Novartis consultancy agreement and honorarium for lecture, Vifor Pharma consultancy agreement.
CW has received personal fees from Boehringer Ingelheim, Akebia, AstraZeneca, Bayer, Eli Lilly, GlaxoSmithKline, Gilead, Merck Sharpe Dohme, Mundipharma, Sanofi-Genzyme, and Vifor Fresenius.
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Expanded details of CVOTs, renal and HF studies in patients with T2D. Overview of diabetes CVOTs, renal outcomes studies and HF studies with glucose-lowering drugs in patients with T2D, including key outcomes and baseline characteristics [15, 16, 18, 20,21,22, 26,27,28,29,30,31,32,33,34,35,36,37, 49,50,51,52,53,54,55, 57,58,59, 62, 63, 68,69,70,71,72, 92, 99, 125].
Continuum of CV risk in T2D. T2D is a risk factor for CVD, and several other risk factors are also often present in patients with T2D, as recognised by guidelines such as those of the ESC . Glucose levels alone can be independently linked to progression of CAD . While progression of cardiac disease is thus a feature of T2D, it may in some cases go undetected due to atypical symptom presentation or so-called ‘silent’ manifestations [152, 153], in the proposed ‘unrecognised diabetic cardiac impairment’ phenomenon . Ultimately, overt CVD or heart failure may develop, both of which are prevalent among people living with T2D [4, 48, 152]. CAD, coronary artery disease; CVD, cardiovascular disease; ESC, European Society of Cardiology; MACE, major adverse cardiovascular events; T2D, type 2 diabetes. Figure S2. What to expect next from CVOT-related research. The results of CVOTs have raised several questions that are now being addressed in clinical and scientific studies, chief among which is: how do glucose-lowering drugs produce glucose-independent beneficial effects on cardiorenal outcomes? CVOT, cardiovascular outcomes trial; GLP-1, glucagon like peptide-1; GLP-1 RA, GLP-1 receptor agonist; SGLT2, sodium–glucose transporter 2.
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Davies, M.J., Drexel, H., Jornayvaz, F.R. et al. Cardiovascular outcomes trials: a paradigm shift in the current management of type 2 diabetes. Cardiovasc Diabetol 21, 144 (2022). https://doi.org/10.1186/s12933-022-01575-9
- Cardiovascular disease
- Cardiovascular outcomes trials
- Chronic kidney disease
- Cardiovascular safety
- Heart failure
- Glucose-lowering drug
- GLP-1 RAs
- Type 2 diabetes
- SGLT2 inhibitors