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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
Cardiovascular Diabetologyvolume 18, Article number: 73 (2019)
The SUSTAIN 6 trial demonstrated that once-weekly semaglutide (0.5 and 1.0 mg) significantly reduced major adverse cardiovascular (CV) events (MACE) vs placebo in subjects with type 2 diabetes (T2D) and high CV risk. The effects of gender, age and baseline CV risk on outcomes are important considerations for further study.
Subjects were grouped according to gender, age (50–65 years and > 65 years), and CV risk profile at baseline (prior myocardial infarction [MI] or stroke vs no prior MI or stroke, and established CV disease [CVD] vs CV risk factors alone, including subjects with chronic kidney disease). Time to MACE and its individual components (CV death, nonfatal MI, nonfatal stroke), hospitalization for unstable angina or heart failure, and revascularization (coronary and peripheral) were analyzed for all subgroups. Additional analyses were performed for gender and age to investigate change from baseline in HbA1c and body weight, as well as tolerability.
A total of 3297 subjects were included. The majority of subjects (60.7%) were male; 43% were > 65 years of age; 41.5% had a history of MI or stroke; and 76.8% had established CVD. Compared with placebo, semaglutide reduced the risk of the first occurrence of MACE and each MACE component consistently across all subgroups (gender, age, and baseline CV risk profile). Revascularizations, HbA1c and body weight were also reduced consistently across all subgroups compared with placebo. Gastrointestinal adverse events in all treatment groups were more common among women than men, but rates of premature treatment discontinuation were similar for both genders.
In this post hoc analysis of SUSTAIN 6, once-weekly semaglutide vs placebo reduced the risk of MACE in all subjects included in the trial, regardless of gender, age, or baseline CV risk profile.
Trial registry Clinicaltrials.gov, Identifying number: NCT01720446, Date of registration: October 29, 2012
Cardiovascular disease (CVD) is the leading cause of morbidity and mortality in people with type 2 diabetes (T2D) [1, 2], and diabetes itself confers a substantial independent risk of coronary heart disease, stroke, and death from other vascular causes . Current diabetes guidelines recommend multifactorial CV risk management and the preferential use of a glucagon-like peptide-1 receptor agonist (GLP-1RA) or sodium–glucose cotransporter-2 inhibitor with proven CV benefits as a first choice add-on to metformin in patients with T2D and established atherosclerotic CVD [2, 4]. Semaglutide is a GLP-1 analogue approved as a once-weekly, subcutaneous treatment for T2D [5, 6]. The phase 3 SUSTAIN (Semaglutide Unabated Sustainability in Treatment of Type 2 Diabetes) clinical trial program evaluated the efficacy and safety of semaglutide in subjects with T2D in a range of patient populations across the continuum of diabetes care [7,8,9,10,11,12,13,14]. In the SUSTAIN 6 CV outcomes trial (CVOT), once-weekly semaglutide (0.5 or 1.0 mg) added to standard of care significantly reduced the occurrence of a first major adverse CV event (MACE: CV death, nonfatal myocardial infarction [MI], or nonfatal stroke) vs placebo over 2 years in 3297 subjects with T2D and high CV risk . Given the increasing emphasis on individualized patient care in the management of T2D , this post hoc analysis assessed the effects of gender, age, and baseline CV risk on the reduction of CV risk in the SUSTAIN 6 trial.
SUSTAIN 6 study design
The design of SUSTAIN 6 (clinicaltrials.gov NCT01720446) has been described previously . In brief, SUSTAIN 6 was a randomized, double-blind, placebo-controlled, parallel-group trial to evaluate once-weekly semaglutide 0.5 or 1.0 mg vs volume-matched placebo over a 104-week treatment period plus a 5-week follow-up period. The trial was conducted in compliance with the International Conference on Harmonisation Good Clinical Practice guidelines and the Declaration of Helsinki [15, 16]. The protocol was approved by local ethics committees and institutional review boards. Written informed consent was obtained from all subjects before trial commencement.
A total of 3297 subjects with T2D (HbA1c ≥ 7%) were randomized to receive once-weekly semaglutide 0.5 or 1.0 mg or placebo for 104 weeks. Subjects were ≥ 50 years of age with established CVD (defined as previous CV, cerebrovascular, or peripheral vascular disease), chronic heart failure (New York Heart Association class II or III), or chronic kidney disease (CKD) of stage 3 or higher, or were ≥ 60 years of age with at least one CV risk factor (microalbuminuria or proteinuria, hypertension and left ventricular hypertrophy, left ventricular systolic or diastolic dysfunction or ankle–brachial index < 0.9). All subjects treated with semaglutide followed a fixed dose-escalation regimen, with a starting dose of 0.25 mg for 4 weeks that escalated to 0.5 mg for 4 weeks until the maintenance dose (0.5 or 1.0 mg) was reached.
The primary composite outcome (MACE) was the first occurrence of death from CV causes, nonfatal MI, or nonfatal stroke. Other outcomes included time to first hospitalization for unstable angina and heart failure, time to first revascularization (coronary or peripheral), and changes in HbA1c and weight. All outcomes were collected after 104 weeks of treatment.
This post hoc analysis examined the effect of gender, age (subjects aged 50–65 and > 65 years), and CV risk profile at baseline on time to first occurrence of MACE, the individual components of MACE (CV death, nonfatal MI, or nonfatal stroke), hospitalization for unstable angina or heart failure, and revascularization. Additional analyses were performed by gender and age to investigate changes from baseline in HbA1c and body weight, adverse events (AEs), and hypoglycemia, as defined by the American Diabetes Association (ADA) .
For comparison of outcomes between men and women, estimated hazard ratios (HRs) and associated confidence intervals (CIs) were determined by a Cox proportional hazards model with an interaction between treatment (semaglutide, placebo) and gender as a fixed factor. Efficacy and safety were assessed by age group using post hoc subgroup analyses of subjects ≤ 65 and > 65 years. Post-baseline responses for time to first occurrence of MACE, CV death, nonfatal MI, nonfatal stroke, hospitalization for unstable angina or heart failure, revascularization, and change from baseline in HbA1c and body weight were analyzed using a mixed model for repeated measurements with interaction between subgroup, randomized treatment, and baseline value as covariate. No adjustment for multiplicity was performed. A significance level for interaction of 5% was considered significant. To investigate more general linear and non-linear effects of age at baseline, individual outcomes and AEs were modelled as a function of age, controlling for randomized treatment and CVD at baseline via negative-binomial log regression (see “Post hoc analysis by age”). Analyses were based on pooled data using semaglutide 0.5 mg and 1.0 mg doses for MACE and its components, hospitalization due to angina or heart failure, revascularization, and AEs. HbA1c and body weight were reported separately for both semaglutide doses following the statistical methods used in the primary SUSTAIN 6 trial .
CV risk profile subgroups
To assess the effect of baseline CV risk profiles on outcomes, two separate subgroup analyses were performed: (1) for subjects who had experienced a prior MI or stroke compared with those who had not, and (2) for those with established CVD, defined as prior stroke, ischemic heart disease (including MI), peripheral arterial disease, ≥ 50% arterial stenosis in any artery, coronary revascularization (percutaneous coronary intervention or coronary artery bypass graft), or heart failure vs those with CV risk factors alone and no manifestations of CVD as defined above. The risk classification in the latter subgroup comparison differs from the prespecified group of evidence of CVD in SUSTAIN 6, in which subjects with CKD stage 3 or higher were included . In this post hoc analysis, however, subjects with CKD were included in the CV risk factor alone group to reflect the usual definition of established CVD used in clinical practice. Statistical analyses were carried out using Cox proportional hazards models for time to first MACE with treatment, and treatment by subgroup interaction, if applicable, as fixed factor(s). No adjustment for multiplicity was performed. A significance level for interaction of 5% was considered significant.
Post hoc analysis by gender
Among 3297 subjects in the SUSTAIN 6 study population, 2002 were male and 1295 were female (Table 1A). There were no clear differences in subject demographics or key baseline characteristics between men and women, with the exception of weight (men tended to be heavier) and smoking status (51.7 vs 26.1% and 56.1 vs 23.0% of men vs women had a history of smoking in the semaglutide and placebo groups, respectively). Similar proportions of male and female subjects completed the trial and treatment. MACE occurred in lower proportions of subjects treated with semaglutide vs placebo in both men and women, and this overall benefit was independent of gender (p = 0.45 for interaction) (Fig. 1). The same pattern was noted across the individual MACE components of CV death, nonfatal MI and nonfatal stroke; lower or similar proportions of both men and women experienced events with semaglutide vs placebo, and p-values for interaction were nonsignificant (p = 0.46, p = 0.34 and p = 0.74, respectively, for each endpoint) (Fig. 1). Gender had no apparent effect on first hospitalization for unstable angina (p = 0.35 for interaction) or heart failure (p = 0.55 for interaction), or time to first revascularization procedure (p = 0.50 for interaction; Fig. 2).
Post hoc analysis by age
In the SUSTAIN 6 study, 1879 subjects were 50–65 years of age and 1418 were > 65 years (Table 1B). There were no clear differences in subject demographics or key baseline characteristics between groups. Duration of diabetes was greater in subjects > 65 years compared with those ≤ 65 years (16.4 vs 12.6 years for the semaglutide group and 15.2 vs 12.4 years for the placebo group). Similar proportions of subjects in each age group completed the trial and treatment. HRs for time to first confirmed MACE were all below 1.0 for subjects treated with semaglutide vs placebo, irrespective of age (p = 0.92 for interaction, Fig. 1). Results were consistent for the individual components of MACE across age groups (Fig. 1; p = 0.35, p = 0.42, and p = 0.45 for interaction, respectively, for CV death, nonfatal MI, and nonfatal stroke). Age had no apparent effect on first hospitalization due to unstable angina (p = 0.16 for interaction), heart failure (p = 0.26 for interaction) or revascularization procedures (p = 0.97 for interaction; Fig. 2). A series of regression analyses were conducted to assess more general linear and nonlinear trends for the incidence of MACE by age; since no significant effects were found, these have not been reported further (see Additional file 1).
Post hoc analysis by CV risk
Pooled key baseline characteristics, CV risk factors, and manifestation of CVD at baseline for the two CV subgroups [subjects with prior MI or stroke vs no prior MI or stroke and subjects with established CVD vs risk factors only (including CKD)] are shown in Table 1C. In total, 1367 subjects had a history of MI or stroke (vs 1930 without prior history) and 2533 had established CVD (vs 764 with CV risk factors only).
Hazard ratios for time to first confirmed MACE were all below 1.0 in subjects treated with semaglutide vs placebo, irrespective of baseline CV risk profile (Fig. 3). Similar results were observed across the individual components of MACE, with the exception of CV death in subjects with a prior MI or stroke or with established CVD (p = 0.22 for interaction between subjects with prior MI or stroke vs no prior MI or stroke; p = 0.52 for interaction between subjects with established CVD vs risk factors only) (Fig. 2).
In the SUSTAIN 6 trial, there was no difference in hospitalization for angina or heart failure between semaglutide and placebo , and this result was independent of baseline CV risk profile (Fig. 2). The between-group interaction for unstable angina in subjects with prior MI or stroke compared with no prior MI or stroke was significant (p = 0.02 for interaction), with a significant reduction in hospitalization for unstable angina for semaglutide vs placebo in subjects with no prior MI or stroke (p = 0.03). No significant interactions were noted for hospitalization for heart failure between the various risk groups (Fig. 2; p = 0.59 for interaction between subjects with prior MI or stroke vs no prior MI or stroke and p = 0.93 for interaction between subjects with established CVD vs CV risk factors only).
Semaglutide reduced time to first revascularization vs placebo in the overall study; this result was observed regardless of baseline CV risk profile, with no significant differences between subgroups (p = 0.25 for interaction between subjects with prior MI or stroke vs no prior MI or stroke and p = 0.27 for interaction between subjects with established CVD vs CV risk factors only).
Reductions in HbA1c and body weight by gender and age
Significantly greater reductions in HbA1c were achieved by subjects treated with semaglutide than by those receiving placebo, and this decrease was consistent for both genders (ETD for semaglutide 0.5 and 1.0 mg vs placebo: − 0.65% [95% CI − 0.80; − 0.49] and − 0.96% [95% CI − 1.11; − 0.81], respectively in males and − 0.75% [95% CI − 0.94; − 0.56] and − 1.09% [95% CI − 1.28; − 0.89], respectively in females; Fig. 4a) and across age groups (ETDs for semaglutide 0.5 and 1.0 mg vs placebo were − 0.72% [95% CI − 0.88; − 0.56] and − 1.13% [95% CI − 1.29; − 0.97], respectively, in ≤ 65 years, and − 0.66% [95% CI − 0.84; − 0.47] and − 0.85% [95% CI − 1.03; − 0.67], respectively, in > 65 years; Fig. 4b). The p-values for all comparisons between gender and age groups were nonsignificant.
Greater weight loss was observed with semaglutide 0.5 and 1.0 mg compared with placebo in both genders (ETD − 2.86 kg [95% CI − 3.52; − 2.19] and − 3.68 kg [95% CI − 4.33; − 3.03] in males and − 3.04 kg [95% CI − 3.85; − 2.23] and − 5.27 kg [95% CI − 6.11; − 4.43] in females; Fig. 4c) and in subjects ≤ 65 and > 65 years of age (ETDs for semaglutide 0.5 and 1.0 mg vs placebo: − 2.90 kg [95% CI − 3.58; − 2.23] and − 3.87 kg [− 4.56; − 3.18], respectively, and − 3.02 kg [− 3.82; − 2.22] and − 4.72 kg [− 5.50; − 3.95], respectively; Fig. 4d). The p-values for all between-group comparisons were nonsignificant.
Adverse effects by gender and age
Similar proportions of men and women reported AEs across treatment groups (Fig. 5). Proportions of serious AEs were comparable between semaglutide and placebo for males (32.5 vs 36.2%) and females (27.9 vs 33.0%). The most frequently reported AEs were gastrointestinal (GI) in nature, and they occurred more often with semaglutide than placebo in both males and females. Female subjects reported more GI AEs in all groups compared with men (55.6 vs 48.5% for semaglutide and 37.7 vs 32.0% for placebo). Comparable proportions of men and women prematurely discontinued treatment due to AEs (12.5 and 13.9%, respectively). A similar proportion of males and females reported hypoglycemia (symptomatic as well as severe) with semaglutide as well as placebo treatment.
To investigate the potential effects of age on AEs, a series of regression analyses were conducted. One in-trial AE type was chosen (GI events) and tested both for treatment-dependent and treatment-independent linear and non-linear effects of age on AE incidence; no clear or consistent patterns or significant effects were found (see Additional file 1).
Treatment guidelines recommend the use of antidiabetes agents with proven CV benefits as second-line therapy in T2D populations with CVD [2, 4, 18]. All currently approved injectable GLP-1RAs have demonstrated CV safety (non-inferiority) in CVOTs [12, 19,20,21,22,23], but only four have demonstrated both CV safety and superiority relative to standard of care [12, 20, 22, 23]. While there appears to be a class effect among human-based GLP-1 analogs with respect to CV benefit, additional studies are needed to further elucidate whether CV protective effects are provided by all GLP-1RAs [24, 25].
Semaglutide has demonstrated a consistent effect with respect to glycemic efficacy and safety in T2D populations across the spectrum of care [7,8,9,10,11,12,13,14, 26,27,28]. In SUSTAIN 6, subjects with T2D at high CV risk treated with semaglutide had a 26% lower risk of the primary composite outcome of first MACE (death from CV causes, nonfatal MI, or nonfatal stroke) vs those receiving placebo over 2 years (p = 0.02 for superiority [post hoc]) . Results of this post hoc analysis of the SUSTAIN 6 trial suggest the beneficial effects of semaglutide vs placebo were similar for men and women, for both younger (50–65 years) and older (> 65) populations studied, and for subjects with varying CV risk profiles at baseline. Similar results were observed with another once-weekly GLP-1RA (exenatide), in which subgroup analyses showed a consistent reduction in MACE across a range of baseline characteristics, including gender, age, and previous CV events . Gender is an important determinant of CV risk within T2D . Historically, women have reached target values for modifiable CV risk factors, including HbA1c, systolic and diastolic blood pressure, and lipid levels, less frequently than men [31,32,33]. In the present post hoc analysis, the decreased risk of first occurrence of MACE associated with semaglutide treatment vs placebo demonstrated in SUSTAIN 6  was comparable for both genders, and overall event rates were similar or lower for women than men. Given the scarcity of available evidence for the effects of T2D treatment on CV outcomes in women and the increased emphasis on CV risk reduction , additional analysis of CV outcome trials in T2D by gender could help individualize optimal care and risk management for all patients with a history of or risk factors for CVD.
Cardiovascular risk reduction in populations > 65 years deserves considerable attention alongside the efficacy and safety associated with any intervention. However, trials specifically examining the effect of antihyperglycemic treatment on CV events in older populations are lacking. In this analysis, treatment with semaglutide reduced the risk of a MACE and its components in subjects aged 50‒65 and > 65 years. Further subgroup analysis in subjects > 75 years could not be conducted due to insufficient numbers for accurate assessment. A post hoc analysis from the LEADER (Liraglutide Effect and Action in Diabetes: Evaluation of Cardiovascular Outcome Results) trial examined the effects of liraglutide vs placebo in subjects aged ≥ 75 years (n = 836) and in those aged 60–74 years (n = 6183) . Treatment with liraglutide led to a greater MACE risk reduction in subjects aged ≥ 75 years (HR: 0.66 [95% CI 0.49; 0.89]) compared with those aged 60‒74 years (HR: 0.95; [95% CI 0.83; 1.09]) (p = 0.05 for interaction).
A pre-existent history of MI or stroke is an important CV risk determinant in subjects with T2D [35, 36]. Therefore, the present post hoc analysis divided subjects based on clinically relevant factors (prior MI or stroke vs no prior MI or stroke and established CVD vs risk factors alone) to allow for exploration of CV outcomes across these CV risk subgroups. Semaglutide demonstrated a consistent reduction in MACE and its components vs placebo, regardless of baseline CV risk profile. These results may be compared with those of a post hoc analysis of the LEADER trial, which demonstrated similar incidence rates of MACE in the liraglutide vs placebo group in subjects with a relatively low baseline CV risk (defined as isolated CKD, hypertension with left ventricular hypertrophy, New York Heart Association Class II or III heart failure, and left ventricular systolic or diastolic dysfunction) . Given the low number of subjects and CV events for subjects without established CVD in both analyses, however, these results should be interpreted with caution. The REWIND (Researching Cardiovascular Events with a Weekly Incretin in Diabetes) trial assessed the effect of dulaglutide, a GLP-1RA, vs placebo added to standard of care in 9901 subjects with T2D. In this trial, the majority of subjects did not have established CVD at baseline, and the highly anticipated results from the trial will add to the body of evidence on the potential role for GLP-1RAs on CV risk reduction in a broad range of individuals with T2D .
The current analysis evaluated the tolerability of semaglutide across genders and both age groups (50‒65 and > 65 years). Overall, a higher proportion of women reported GI AEs compared with men, although the rate difference between semaglutide and placebo groups was similar for both. Of note, the rate of premature treatment discontinuation due to AEs was comparable between genders, suggesting that the higher reported occurrence of GI AEs in women did not result in increased drug discontinuation. While it is necessary to examine the safety of semaglutide in older populations with T2D, especially in those at risk for retinopathy or kidney complications, these points are not discussed in this analysis and will be explored in future trials [39, 40].
Limitations of the current analysis include the relatively short duration of follow-up (2.1 years) and the relatively small number of MACE, both in the semaglutide group (108/1648 subjects; 6.6%) and in subjects randomized to receive placebo (146/1649 subjects; 8.9%), leading to weaker statistical power in the subgroup results. In addition, the older age group in SUSTAIN 6 included both those with established CVD and those with CV risk factors alone, while the younger group of subjects included only those with established CVD. These differences limit the ability to make assumptions about the consistency of clinical benefit in older T2D populations at high CV risk. However, when CV risk composition of all subjects in these groups was explored in this subgroup analysis, the results suggested a similarity irrespective of age. Finally, considering the nature of subgroup analyses and the risk of false positive effects with a large number of comparisons , any conclusions should be interpreted cautiously and in the context of all available data in the literature.
In this post hoc analysis of the SUSTAIN 6 trial, once-weekly semaglutide vs placebo reduced the risk of MACE in all subjects regardless of gender, age (50‒65 and > 65 years), or baseline CV risk profile (prior MI or stroke vs no prior MI or stroke or established CVD vs CV risk factors alone). In addition, similar reductions in HbA1c and weight were observed with semaglutide compared with placebo across gender and age groups, and safety profiles were comparable between men and women and in subjects above or below the age of 65 years.
Availability of data and materials
The subject level analysis data sets for the research presented in the publication are available from the corresponding author on reasonable request.
American Diabetes Association
chronic kidney disease
estimated treatment difference
glucagon-like peptide-1 receptor agonist
major adverse cardiac event
type 2 diabetes
American Diabetes Association. Standards of medical care in diabetes 2018. Diabetes Care. 2018;41(Suppl 1):S1–135.
American Diabetes Association. Cardiovascular disease and risk management: standards of medical care in diabetes 2019. Diabetes Care. 2019;42(Suppl 1):S103–23.
Sarwar N, Gao P, Seshasai SR, Gobin R, Kaptoge S, Di Angelantonio E, et al. Diabetes mellitus, fasting blood glucose concentration, and risk of vascular disease: a collaborative meta-analysis of 102 prospective studies. Lancet. 2010;375:2215–22.
Davies MJ, D’Alessio DA, Fradkin J, Kernan WN, Mathieu C, Mingrone G, et al. Management of hyperglycemia in type 2 diabetes, 2018. A consensus report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD). Diabetes Care. 2018;2018(41):2669–701.
Lau J, Bloch P, Schäffer L, Pettersson I, Spetzler J, Kofoed J, et al. Discovery of the once-weekly glucagon-like peptide-1 (GLP-1) analogue semaglutide. J Med Chem. 2015;58:7370–80.
Ozempic marketing authorisation 2018. https://www.ema.europa.eu/en/medicines/human/EPAR/ozempic. Accessed 7 May 2019.
Sorli C, Harashima SI, Tsoukas GM, Unger J, Karsbøl JD, Hansen T, et al. Efficacy and safety of once-weekly semaglutide monotherapy versus placebo in patients with type 2 diabetes (SUSTAIN 1): a double-blind, randomised, placebo-controlled, parallel-group, multinational, multicentre phase 3a trial. Lancet Diabetes Endocrinol. 2017;5:251–60.
Ahrén B, Masmiquel L, Kumar H, Sargin M, Karsbøl JD, Jacobsen SH, et al. Efficacy and safety of once-weekly semaglutide versus once-daily sitagliptin as an add-on to metformin, thiazolidinediones, or both, in patients with type 2 diabetes (SUSTAIN 2): a 56-week, double-blind, phase 3a, randomised trial. Lancet Diabetes Endocrinol. 2017;5:341–54.
Ahmann AJ, Capehorn M, Charpentier G, Dotta F, Henkel E, Lingvay I, et al. Efficacy and safety of once-weekly semaglutide versus exenatide ER in subjects with type 2 diabetes (SUSTAIN 3): a 56-week, open-label, randomized clinical trial. Diabetes Care. 2018;41:258–66.
Aroda VR, Bain SC, Cariou B, Piletić M, Rose L, Axelsen M, et al. Efficacy and safety of once-weekly semaglutide versus once-daily insulin glargine as add-on to metformin (with or without sulfonylureas) in insulin-naive patients with type 2 diabetes (SUSTAIN 4): a randomised, open-label, parallel-group, multicentre, multinational, phase 3a trial. Lancet Diabetes Endocrinol. 2017;5:355–66.
Rodbard HW, Lingvay I, Reed J, de la Rosa R, Rose L, Sugimoto D, et al. Semaglutide added to basal insulin in type 2 diabetes (SUSTAIN 5): a randomized, controlled trial. J Clin Endocrinol Metab. 2018;103:2291–301.
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.
Pratley RE, Aroda VR, Lingvay I, Lüdemann J, Andreassen C, Navarria A, et al. Semaglutide versus dulaglutide once weekly in patients with type 2 diabetes (SUSTAIN 7): a randomised, open-label, phase 3b trial. Lancet Diabetes Endocrinol. 2018;6:275–86.
Zinman B, Bhosekar V, Busch R, Holst I, Ludvik B, Thielke D, et al. Semaglutide once weekly as add-on to SGLT-2 inhibitor therapy in type 2 diabetes (SUSTAIN 9): a randomised, placebo controlled trial. Lancet Diab Endocrinol. 2019;7:356–67.
International Conference on Harmonisation-World Health Organization Guideline for Good Clinical Practice. ICH harmonised tripartite guideline good clinical practice 2016. https://www.ich.org/products/guidelines/efficacy/efficacy-single/article/integrated-addendum-good-clinical-practice.html. Accessed 22 Mar 2019.
World Medical Association. World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects. JAMA. 2013;310:2191–4.
Seaquist ER, Anderson J, Childs B, Cryer P, Dagogo-Jack S, Fish L, et al. Hypoglycemia and diabetes: a report of a workgroup of the American Diabetes Association and the Endocrine Society. Diabetes Care. 2013;36:1384–95.
Shehadeh N, Raz I, Nakhleh A. Cardiovascular benefit in the limelight: shifting type 2 diabetes treatment paradigm towards early combination therapy in patients with overt cardiovascular disease. Cardiovasc Diabetol. 2018;17:117.
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.
Marso SP, Daniels GH, Brown-Frandsen K, Kristensen P, Mann JF, 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.
Hernandez AF, Green JB, Janmohamed S, D’Agostino RB Sr, 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. 2018;392:1519–29.
Eli Lilly Press release, 2018. Trulicity® (dulaglutide) demonstrates superiority in reduction of cardiovascular events for broad range of people with type 2 diabetes. https://investor.lilly.com/node/39796/pdf. Accessed May 2018.
Zhang Z, Chen X, Lu P, Zhang J, Xu Y, He W, et al. Incretin-based agents in type 2 diabetic patients at cardiovascular risk: compare the effect of GLP-1 agonists and DPP-4 inhibitors on cardiovascular and pancreatic outcomes. Cardiovasc Diabetol. 2017;16:31.
Li Y, Rosenblit PD. Glucagon-like peptide-1 receptor agonists and cardiovascular risk reduction in type 2 diabetes mellitus: is it a class effect? Curr Cardiol Rep. 2018;20:113.
Witkowski M, Wilkinson L, Webb N, Weids A, Glah D, Vrazic H. A systematic literature review and network meta-analysis comparing once-weekly semaglutide with other GLP-1 receptor agonists in patients with type 2 diabetes previously receiving 1–2 oral anti-diabetic drugs. Diabetes Ther. 2018;9:1149–67.
Aroda V, Ahmann A, Cariou B, Chow F, Davies MJ, Jódar E, et al. Comparative efficacy, safety, and cardiovascular outcomes with once-weekly subcutaneous semaglutide in the treatment of type 2 diabetes: insights from the SUSTAIN 1–7 trials. Diabetes Metab. 2019. https://doi.org/10.1016/j.diabet.2018.12.001 (Epub ahead of print).
Mishriky BM, Cummings DM, Powell JR, Sewell KA, Tanenberg RJ. Comparing once-weekly semaglutide to incretin-based therapies in patients with type 2 diabetes: a systematic review and meta-analysis. Diabetes Metab. 2019;45:102–9.
Mentz RJ, Bethel MA, Merrill P, Lokhnygina Y, Buse JB, Chan JC, et al. Effect of once-weekly exenatide on clinical outcomes according to baseline risk in patients with type 2 diabetes mellitus: insights from the EXSCEL trial. J Am Heart Assoc. 2018;7:e009304.
Peters SA, Huxley RR, Woodward M. Diabetes as risk factor for incident coronary heart disease in women compared with men: a systematic review and meta-analysis of 64 cohorts including 858,507 individuals and 28,203 coronary events. Diabetologia. 2014;57:1542–51.
Gouni-Berthold I, Berthold HK, Mantzoros CS, Böhm M, Krone W. Sex disparities in the treatment and control of cardiovascular risk factors in type 2 diabetes. Diabetes Care. 2008;31:1389–91.
Kautzky-Willer A, Kamyar MR, Gerhat D, Handisurya A, Stemer G, Hudson S, et al. Sex-specific differences in metabolic control, cardiovascular risk, and interventions in patients with type 2 diabetes mellitus. Gend Med. 2010;7:571–83.
Sekerija M, Poljicanin T, Erjavec K, Liberati-Cizmek AM, Prasek M, Metelko Z. Gender differences in the control of cardiovascular risk factors in patients with type 2 diabetes—a cross-sectional study. Intern Med. 2012;51:161–6.
Gilbert MP, Bain SC, Franek E, Jodar-Gimeno E, Nauck MA, Pratley R, et al. Effect of liraglutide on cardiovascular outcomes in elderly patients: a post hoc analysis of a randomized controlled trial. Ann Intern Med. 2018. https://doi.org/10.7326/m18-1569.
National Diabetes Statistics Report. 2017. https://www.cdc.gov/diabetes/pdfs/data/statistics/national-diabetes-statistics-report.pdf. Accessed 7 May 2019.
Bhatt DL, Eagle KA, Ohman EM, Hirsch AT, Goto S, Mahoney EM, et al. Comparative determinants of 4-year cardiovascular event rates in stable outpatients at risk of or with atherothrombosis. JAMA. 2010;304:1350–7.
Verma S, Poulter NR, Bhatt DL, Bain SC, Buse JB, Leiter LA, et al. Effects of liraglutide on cardiovascular outcomes in patients with type 2 diabetes mellitus with or without history of myocardial infarction or stroke. Circulation. 2018;138:2884–94.
Gerstein HC, Colhoun HM, Dagenais GR, Diaz R, Lakshmanan M, Pais P, et al. Design and baseline characteristics of participants in the Researching cardiovascular Events with a Weekly INcretin in Diabetes (REWIND) trial on the cardiovascular effects of dulaglutide. Diabetes Obes Metab. 2018;20:42–9.
NCT03811561. https://clinicaltrials.gov/ct2/show/NCT03811561. Accessed 7 May 2019.
NCT03819153. https://clinicaltrials.gov/ct2/show/NCT03819153. Accessed 7 May 2019.
Wang R, Lagakos SW, Ware JH, Hunter DJ, Drazen JM. Statistics in medicine—reporting of subgroup analyses in clinical trials. N Engl J Med. 2007;357:2189–94.
We thank all the patients, investigators, and trial-site staff members who were involved in the conduct of the trial; and Sherri Vanderveen, AXON Communications, for medical writing and editorial assistance (funded by Novo Nordisk).
This study was supported by Novo Nordisk A/S, Denmark. The funding sources contributed to the design and conduct of the trial, the analysis and interpretation of the data, review and approval of the manuscript.
Ethics approval and consent to participate
The protocol was approved by local ethics committees and institutional review boards at each participating center. All subjects provided written informed consent.
Consent for publication
During the conduct of the study, L.A.L. received research grants to his institution from Novo Nordisk. Outside of the submitted work, he has received grants and/or personal fees for advisory panels, speakers’ bureaus, and research support from AstraZeneca, Boehringer Ingelheim, Eli Lilly, Janssen Pharmaceuticals, Merck, Novo Nordisk, and Sanofi. He also reports research grants from GlaxoSmithKline and personal fees for advisory panels from Servier.
Outside the submitted work, S.C.B. has received honoraria, teaching, and research sponsorship/grants from Abbott, AstraZeneca, Boehringer Ingelheim, Cellnovo, Eli Lilly, Merck Sharp & Dohme, Novo Nordisk, and Sanofi-aventis, Cardiff University, Doctors.net, Elsevier, Onmedica, Omnia-Med, Medscape, All-Wales Medicines Strategy Group, National Institute for Health and Care Excellence (NICE) UK, and Glycosmedia.
Outside the submitted work, I.H. reports research grants and/or personal fees from AstraZeneca/Bristol-Myers Squibb, Boehringer Ingelheim, Dexcom, Eli Lilly, GlaxoSmithKline, Insulet Corp, Janssen Pharmaceuticals, Lexicon Pharmaceuticals, Medtronic, Merck & Co Inc, Population Health Research Institute, Roche Pharma, Sanofi, and Takeda.
E.J. reports grants and personal fees from Novo Nordisk during the conduct of the study. He also reports grants and personal fees as a consultant and/or speaker from Amgen, AstraZeneca, Boehringer Ingelheim, Faes Farma, Fresenius, Janssen Pharmaceuticals, Eli Lilly, Merck Sharp & Dohme, Novartis, Novo Nordisk, Pfizer, Sanofi, Shire, and UCB.
Outside of the submitted work, S.M. has received honoraria and/or lecture fees from AstraZeneca, Boehringer Ingelheim, Bristol-Meyers Squibb, Eli Lilly, Intarcia Therapeutics, Johnson & Johnson, Merck Sharp & Dohme, Novartis, Novo Nordisk, and Sanofi Aventis. He has also received a research grant from Novo Nordisk and Boehringer Ingelheim.
T.G., T.H., and I.H. report that they are full-time employees of Novo Nordisk A/S.
I.L. received research grants to her institution and consulting fees from Novo Nordisk during the conduct of the study. Outside the submitted work, she has received grants and/or personal fees from AstraZeneca, Boehringer Ingelheim, Eli Lilly, GI Dynamics, Intarcia, Mannkind, Merck, Mylan, Novartis, NovoNordisk, Pfizer, Sanofi, TARGETPharma, and Valeritas.
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