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Relation of insulin treatment for type 2 diabetes to the risk of major adverse cardiovascular events after acute coronary syndrome: an analysis of the BETonMACE randomized clinical trial

Cardiovascular Diabetology volume 20, Article number: 125 (2021) Cite this article

Abstract

Background

In stable patients with type 2 diabetes (T2D), insulin treatment is associated with elevated risk for major adverse cardiovascular events (MACE). Patients with acute coronary syndrome (ACS) and T2D are at particularly high risk for recurrent MACE despite evidence-based therapies. It is uncertain to what extent this risk is further magnified in patients with recent ACS who are treated with insulin. We examined the relationship of insulin use to risk of MACE and modification of that risk by apabetalone, a bromodomain and extra-terminal (BET) protein inhibitor.

Methods

The analysis utilized data from the BETonMACE phase 3 trial that compared apabetalone to placebo in patients with T2D, low HDL cholesterol, andACS. The primary MACE outcome (cardiovascular death, myocardial infarction, or stroke) was examined according to insulin treatment and assigned study treatment. Multivariable Cox regression was used to determine whether insulin use was independently associated with the risk of MACE.

Results

Among 2418 patients followed for median 26.5 months, 829 (34.2%) were treated with insulin. Despite high utilization of evidence-based treatments including coronary revascularization, intensive statin treatment, and dual antiplatelet therapy, the 3-year incidence of MACE in the placebo group was elevated among insulin-treated patients (20.4%) compared to those not-treated with insulin (12.8%, P = 0.0001). Insulin treatment remained strongly associated with the risk of MACE (HR 2.10, 95% CI 1.42–3.10, P = 0.0002) after adjustment for demographic, clinical, and treatment variables. Apabetalone had a consistent, favorable effect on MACE in insulin-treated and not insulin-treated patients.

Conclusion

Insulin-treated patients with T2D, low HDL cholesterol, and ACS are at high risk for recurrent MACE despite the use of evidence-based, contemporary therapies. A strong association of insulin treatment with risk of MACE persists after adjustment for other characteristics associated with MACE. There is unmet need for additional treatments to mitigate this risk.

Trial registration ClinicalTrials.gov NCT02586155, registered October 26, 2015

Introduction

Patients with acute coronary syndrome (ACS) are at high risk for additional major adverse cardiovascular events (MACE). Patients with type 2 diabetes comprise approximately 30% of those with ACS and experience up to twice the risk of recurrent MACE as those without type 2 diabetes [1,2,3].

Chronic insulin treatment is required in approximately 25% of patients with type 2 diabetes to control hyperglycemia [4]. Among patients with type 2 diabetes and ACS, approximately 35% receive chronic insulin treatment [5,6,7]. In patients with type 2 diabetes who have not had prior MACE or who have stable coronary heart disease, insulin use is associated with elevated risk of incident or recurrent MACE and death despite use of evidence-based cardiovascular therapies [8,9,10,11]. However, the extent to which insulin treatment is associated with elevated cardiovascular risk after ACS is uncertain. Moreover, no diabetes medication has been shown to reduce MACE after ACS. Medications that have shown favorable cardiovascular effects in stable patients have not been studied after ACS [metformin, sodium–glucose loop transporter-2 (SGLT2) inhibitors] and drugs in other classes that have been studied after ACS failed to show benefit [glucagon-like peptide-1 (GLP-1) receptor agonists, dipeptidyl peptidase-4 inhibitors] [6, 12].

Bromodomain and extra-terminal (BET) proteins are epigenetic regulators of gene transcription. Apabetalone is a selective BET protein inhibitor with potentially salutary effects on pathways implicated in inflammation, endothelial dysfunction, thrombosis, and vascular calcification [13,14,15]. These injurious processes are prognostically important in patients with ACS [16]. Phase 2 clinical data suggested that apabetalone might have favorable effects on MACE, particularly among those with type 2 diabetes [17]. Accordingly, the phase 3 BETonMACE trial [7] was designed to compare apabetalone with placebo in patients with type 2 diabetes and recent ACS. The present analysis used data from BETonMACE to determine the association of insulin use with risk of MACE after ACS in a contemporary cohort of patients receiving evidence-based background cardiovascular treatments. In addition, we evaluated the interaction of insulin use and apabetalone on that risk.

Methods

Study design

The design and principal results of the BETonMACE trial have been described [7, 18]. The study was approved by the responsible institutional review board at each participating site, and each patient gave written, informed consent. In brief, inclusion criteria were age at least 18 years, ACS within the preceding 7–90 days, low high-density lipoprotein cholesterol (HDL-C) levels, and a diagnosis of type 2 diabetes. Concomitant high-intensity statin therapy with atorvastatin 40–80 mg or rosuvastatin 20–40 mg daily was required unless a lower dose was medically indicated. Other concomitant treatments, including therapies for type 2 diabetes, were assessed at the randomization and subsequent visits. Patients with a prescription for any insulin product were considered to be insulin-treated. Eligible patients were randomized to treatment with apabetalone 100 mg twice daily or matching placebo. The trial continued until a blinded clinical events committee determined that at least 250 patients had experienced the primary MACE outcome (cardiovascular death, non-fatal myocardial infarction or non-fatal stroke). Secondary endpoints included hospitalization for heart failure. Adverse and serious adverse events, including hypoglycemia, were reported by investigators and categorized according to the Medical Dictionary for Regulatory Activities (MedDRA).

Statistical analysis

This was a post hoc analysis. Baseline characteristics were summarized as percentages for dichotomous data and means (SDs) for approximately normal or medians (IQRs) for non-normal continuous data. Characteristics were compared between patients with diabetes who were or were not treated with insulin during the trial using t-tests or Wilcoxson tests for continuous variables and chi-square tests for categorical variables.

The cumulative incidence of the primary MACE endpoint was described in each treatment group and insulin use subgroup with Kaplan–Meier survival analysis. Cox proportional hazards models were used to determine treatment hazard ratios (HR) with 95% confidence interval (CI) and interaction of study treatment and insulin treatment on MACE.

Cox regression models were used to determine whether insulin treatment was an independent predictor of MACE and hospitalization for heart failure in the placebo group. Model 1 was stratified for country and baseline statin allocation. Model 2 was adjusted for demographic variables (age, sex, race) and other characteristics that differed between insulin-treated and not insulin-treated patients including duration of diabetes; history of heart failure, myocardial infarction, or coronary revascularization procedure prior to the qualifying ACS; statin treatment intensity, and hemoglobin A1c. Model 3 was also adjusted for the variables in model 2 plus use of metformin, sulfonylureas, sodium–glucose cotransporter-2 (SGLT2) inhibitors, and glucagon-like peptide-1 (GLP-1) receptor agonists.

Heterogeneity in the absolute difference in risk of MACE with apabetalone versus placebo according to insulin treatment category was determined according to equation 5 for quantitative interaction in the treatise of Gail and Simon [19]. The occurrence of adverse events related to hypoglycemia in insulin-treated versus not insulin-treated patients and of MACE among those with or without hypoglycemia were compared with Fisher’s exact test. Other analyses were performed with R software, version 3.5.1 or higher (R Foundation for Statistical Computing). P-values less than 0.05 were considered statistically significant.

Results

The analysis cohort comprised 2418 patients who were randomized at 190 sites in 13 countries between November 2015 and July 2018, received at least one dose of study medication, and were followed for a median of 26.5 months. Overall, there were 274 primary MACE endpoints with 125 (10.9%) in the apabetalone group and 149 (12.4%) in the placebo group (treatment HR 0.82; 95% CI 0.65–1.04; P = 0.11) [7]. There were 78 patients with hospitalization for heart failure, with 29 (2.4%) in the apabetalone group and 49 (4.0%) in the placebo group (treatment HR 0.59; 95% CI 0.38–0.94; P = 0.03) [20].

Baseline characteristics of the analysis cohort are summarized in Table 1. There were 829 (34.3%) insulin-treated patients and 1589 (65.7%) who were not insulin-treated. Insulin-treated patients were more likely to be female, of non-white race, to have a longer duration of diabetes and a history of heart failure, to have a prior history of myocardial infarction or coronary revascularization, and to receive high-intensity statin treatment. Insulin-treated patients had higher baseline levels of fasting glucose and hemoglobin A1c than patients not treated with insulin. Insulin-treated patients were less likely to be treated with metformin or sulfonylureas, but more likely to be treated with SGLT2 inhibitors or GLP-1 receptor agonists.

Table 1 Baseline characteristics of the patients according to insulin treatment
Full size table

The Fig. 1 shows the cumulative incidence of MACE by insulin treatment category and study treatment group. Among patients assigned to placebo, Kaplan–Meier estimates of the incidence of MACE at 3 years were 20.4% in the insulin-treated subgroup and 12.8% in the not insulin-treated subgroup (relative risk 1.59; P = 0.0001). Apabetalone had a similar effect on the relative risk of MACE in the insulin-treated subgroup (treatment HR 0.80; 95% CI 0.57–1.14) and in the not insulin-treated subgroup (HR 0.85; 95% CI 0.61–1.18; Pinteraction = 0.78). However, due to the higher absolute risk of MACE in the former subgroup, the 3-year Kaplan–Meier estimate of the absolute difference in risk of MACE between apabetalone and placebo groups was twice as great (3.6%) as in the not insulin-treated subgroup (1.8%; P = 0.006 for heterogeneity).

Fig. 1
figure 1

Cumulative incidence of MACE by study treatment group and insulin treatment category. Kaplan–Meier plots showing the cumulative incidence of MACE in the apabetalone and placebo groups, according to insulin treatment category. Hazard ratio are calculated by Cox proportional hazards models, stratified by country (countries with fewer than 100 patients combined) and statin agent (atorvastatin or rosuvastatin). Solid lines, insulin-treated. Dashed lines, not insulin-treated. MACE, major adverse cardiovascular events. Apabetalone had a larger effect on absolute risk of MACE among insulin-treated than not insulin-treated patients (quantitative interaction P = 0.006)

Full size image

Table 2 shows the results of Cox proportional hazards models relating insulin treatment to the risk of MACE and hospitalization for heart failure in the placebo group. Insulin use was a significant predictor of MACE in unadjusted and adjusted models. In fully adjusted Model 3 the use of insulin was associated with a HR for MACE of 2.10 (95% CI 1.42–3.10; P = 0.0002). Insulin use was also a significant predictor of hospitalization for heart failure with HR 2.34 (95% CI 1.19–4.60; P = 0.01) in the fully adjusted model.

Table 2 Cox proportional hazards models for the association of insulin treatment with risk of MACE and hospitalization for heart failure in the placebo group
Full size table

The incidence of treatment-emergent adverse events (TEAE) (i.e., adverse events that developed or worsened during randomized treatment) was greater in patients treated with insulin than in those not treated with insulin (79% versus 62%), with the difference driven by cardiovascular (28% versus 20%) and hematologic (7% versus 3%) events. Similarly, serious TEAE (those that were fatal, life-threatening, required or prolonged hospitalization, or led to disability) occurred in 39% of insulin-treated versus 23% of not insulin-treated patients. TEAE rates were similar in apabetalone versus placebo groups among patients treated with insulin (77% versus 82%) or not treated with insulin (64% versus 61%) as were serious TEAE rates.

Adverse events related to hypoglycemia were more common in insulin-treated patients (n = 26, 3.1%) than in patients not treated with insulin (n = 11, 0.7%, P < 0.001). There was 1 serious adverse event related to hypoglycemia, in an insulin-treated patient. The number of patients with a hypoglycemia-related adverse event was similar with apabetalone or placebo (17 vs. 20). Hypoglycemia did not appear to account for the increased risk of MACE in insulin-treated patients. Among the 26 insulin-treated patients with a hypoglycemia-related adverse event, MACE occurred in 5 (19.2%). Among the 803 insulin-treated patients without a hypoglycemia-related adverse event, MACE occurred in 124 (15.4%, P = 0.58).

Discussion

Insulin treatment has been associated with elevated risk for incident or recurrent MACE in patients with type 2 diabetes without or with established, stable atherosclerotic cardiovascular disease [8,9,10,11]. Patients with ACS are at high risk of further ischemic cardiovascular events. This risk is magnified approximately twofold among patients with type 2 diabetes [1,2,3]. The present analysis demonstrates that risk is even further magnified in insulin-treated patients with type 2 diabetes and ACS, with a 3-year incidence of cardiovascular death, myocardial infarction, or stroke of approximately 20%. This elevated risk persists despite high utilization of contemporary, evidence-based treatments for ACS including coronary revascularization, intensive statin therapy, inhibitors of the renin-angiotensin system, and dual anti-platelet agents and with good control of blood pressure and low-density lipoprotein cholesterol levels. Insulin use was also associated with a significantly increased risk of hospitalization for heart failure, even after adjustment for prior heart failure.

Insulin treatment was associated with other characteristics generally associated with high cardiovascular risk, including prior myocardial infarction, coronary revascularization, and heart failure and longer duration of diabetes. In particular, a longer duration of diabetes may be associated with more severe or extensive atherosclerosis [21,22,23]. Insulin use was also associated with higher levels of hemoglobin A1c and fasting glucose and lower utilization of metformin and sulfonylureas. On the other hand, insulin use was also associated with greater utilization of SGLT2 inhibitors and GLP-1 receptor agonists which might be expected to reduce risk of recurrent MACE and heart failure events. However, adjustment for all of these variables and demographic characteristics did not diminish the strength of association of insulin treatment with risk of MACE and hospitalization for heart failure. We cannot exclude the possibility that other, unidentified covariates account in part for the remaining association.

Insulin may also have direct adverse cardiovascular effects. Exogenous insulin therapy may cause hypoglycemia and in turn increased risk of MACE and death [24,25,26]. Insulin also promotes pathologic cell growth and proliferation in the arterial wall [27]. Intravascular ultrasound shows that insulin-treated patients with coronary artery disease have smaller external elastic membrane and lumen volumes than patients not treated with insulin, resulting in greater percent atheroma volume for a given total atheroma volume [28]. In a favorable direction, insulin treatment reduces the concentration of circulating free fatty acids [29] and thereby might attenuate deleterious effects of elevated free fatty acids on endothelial function, intensity of inflammation, blood pressure, and sudden cardiac death [30, 31].

The only randomized, prospective trial evaluating effects of long-term insulin treatment on risk of MACE following ACS in patients with type 2 diabetes indicated no benefit and the possibility of harm. The Diabetes Mellitus Insulin Glucose Infusion in Acute Myocardial Infarction 2 (DIGAMI-2) trial comprised 1253 patients of whom 947 were randomly assigned to insulin-based or conventional glucose control at hospital discharge after receiving 24 h of insulin–glucose infusion in hospital. Two year mortality was high but did not differ significantly between groups (23.4% versus 21.2%) [32]. In extended follow-up at a median 4.1 years, insulin-based treatment was also associated with a non-significant excess of deaths (odds ratio 1.30, 95% CI 0.93–1.81) and with a significant excess of non-fatal MACE (odds ratio 1.89, 95% CI 1.35–2.63) [33]. Other diabetes drugs evaluated in large randomized, placebo-controlled trials in patients with ACS also failed to show benefit, including lixisenatide [6], alogliptin [12], and aleglitazar [5].

Limitations

Limitations include the fact that the analysis was conducted on a post hoc basis and the trial had limited power to draw inference on event rates and treatment effects in subgroups. Cox models were adjusted for characteristics that differed between patients who were or were not treated with insulin. However, the possibility of residual confounding by unmeasured clinical or laboratory variables cannot be excluded. Changes in the doses of diabetes medications were not ascertained. Only 3.1% of insulin-treated patients had an investigator-reported adverse event related to hypoglycemia and these patients accounted for only 5 MACE events; however, some hypoglycemic events may not have been reported and may have contributed to a higher rate of MACE in insulin-treated patients. Patients in the BETonMACE trial were randomized 7–90 days after the qualifying ACS event; i.e., at hospital discharge or thereafter. The current analysis therefore does not consider potential effects of insulin use during hospitalization for ACS and associated revascularization procedures [34]. Patients in the trial had low levels of HDL cholesterol; it is uncertain whether findings were influenced by this selection criterion.

Conclusion

Insulin treatment is required in many patients with type 2 diabetes and ACS. Notwithstanding the above limitations, insulin use is strongly associated with risks of recurrent MACE and hospitalization for heart failure following ACS, even after adjustment for other characteristics associated with these risks and despite widespread use of evidence-based therapies including coronary revascularization, intensive statin treatment, inhibitors of the renin–angiotensin system, and dual-antiplatelet agents. Because no diabetes drug has shown cardiovascular benefit in patients with recent ACS, the present observations highlight a need for new treatments to reduce MACE and heart failure events in this very high-risk setting.

Apabetalone is a selective BET protein inhibitor with potentially salutary effects on pathways implicated in inflammation, endothelial dysfunction, thrombosis, and vascular calcification [13,14,15]. In patients with type 2 diabetes, low HDL cholesterol, and recent ACS, the BETonMACE study showed a trend to decreased risk of MACE with apabetalone and fewer heart failure hospitalizations compared to placebo [7, 20]. The large absolute difference in the incidence of MACE with apabetalone versus placebo among insulin-treated patients suggests that this group might derive benefit and warrants further study.

Data availability

The authors declare that the data supporting the findings of this study are available within the article.

Abbreviations

ACS:

Acute coronary syndrome

BET:

Bromodomain and extra-terminal domain

DIGAMI-2:

Diabetes Mellitus Insulin Glucose Infusion in Acute Myocardial Infarction 2

GLP-1:

Glucagon-like peptide-1

MACE:

Major adverse cardiovascular events

SGLT2:

Sodium–glucose cotransporter-2

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Acknowledgements

The authors thank the investigators, study site staff, and patient volunteers who participated in the study.

Funding

The BETonMACE trial was funded by Resverlogix Corporation.

Author information

Authors and Affiliations

  1. Division of Cardiology, University of Colorado School of Medicine, 1700 N. Wheeling St. (Cardiology 111B), Aurora, CO, 80045, USA

    Gregory G. Schwartz

  2. Victorian Heart Institute, Monash University, Melbourne, Australia

    Stephen J. Nicholls

  3. Cicarrone Center for the Prevention of Cardiovascular Disease, Johns Hopkins University School of Medicine, Baltimore, MD, USA

    Peter P. Toth

  4. CGH Medical Center Sterling, Sterling, IL, USA

    Peter P. Toth

  5. Resverlogix Corporation, Calgary, AB, Canada

    Michael Sweeney, Christopher Halliday, Jan O. Johansson, Norman C. W. Wong & Ewelina Kulikowski

  6. Division of Nephrology and Hypertension, University of California Irvine, Orange, CA, USA

    Kamyar Kalantar-Zadeh

  7. Department of Medicine, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY, USA

    Henry N. Ginsberg

  8. Imperial Centre for Cardiovascular Disease Prevention, Imperial College, London, UK

    Kausik K. Ray

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  1. Gregory G. Schwartz
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Contributions

Conception of this work: GGS. Design of the clinical trial: GGS, SJN, PPT, JJ, MS, NCWW, KKZ, HNG, KKR. Acquisition of the data: GGS, SJN, PPT, JJ, MS, NCWW, KKZ, HNG, KKR. Analysis of the data: CH. Interpretation of the data: All. Drafting of the manuscript: GGS. Critical revision of the manuscript: All. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Gregory G. Schwartz.

Ethics declarations

Ethics approval and consent to participate

The BETonMACE trial was approved by the responsible institutional review board at each participating site and each patient gave written, informed consent.

Consent for publication

All authors have reviewed and approved the content of this manuscript for publication. A portion of this work was presented in abstract form at the American Heart Association Scientific Sessions, November 2020.

Competing interests

GGS has received research support to the University of Colorado from AstraZeneca, Resverlogix, Roche, Sanofi, and The Medicines Company. He is coinventor of pending US patent 62/806,313 (“Methods for Reducing Cardiovascular Risk”) assigned in full to the University of Colorado. SJN reports research grants from AstraZeneca, Amgen, Anthera, Eli Lilly, Esperion, Novartis, Cerenis, The Medicines Company, Resverlogix, InfraReDx, Roche, Sanofi-Regeneron and LipoScience and honoraria from AstraZeneca, Akcea, Eli Lilly, Anthera, Omthera, Merck, Takeda, Resverlogix, Sanofi-Regeneron, CSL Behring, Esperion, Boehringer Ingelheim. PPT reports speaker bureau compensation from Amarin, Amgen, Esperion, Merck, Novo-Nordisk; consultant compensation from Amarin, Amgen, bio89, Novartis, and Theravance. CH, JJ, EK, MS, and NCWW are employees of Resverlogix Corporation. KKZ has received honoraria from Abbott, Abbvie, ACI Clinical, Akebia, Alexion, Amgen, Ardelyx, Astra-Zeneca, Aveo, Braun, Cara Therapeutics, Chugai, Cytokinetics, Daiichi, DaVita, Fresenius, Genentech, Haymarket Media, Hospira, Kabi, Keryx, Kissei, Novartis, Pfizer, Regulus, Relypsa, Resverlogix, Dr. Schaer, Sandoz, Sanofi, Shire, Vifor, UpToDate, and ZS-Pharma. HNG has received research support from AstraZeneca, Amgen, Pfizer and honoraria from Astrazeneca, Amgen, Pfizer, Merck, Kowa, Resverlogix, Regeneron, Sanofi. KKR reports honoraria from Resverlogix, Aegerion, Amgen, Pfizer, AstraZeneca, Cerenis, Akcea, The Medicines Company, Kowa, Novartis, Cipla, Eli Lilly, Algorithm, Takeda, Boehringer Ingelheim, Abbvie, Silence Therapeutics, Dr. Reddys, Bayer, Daiichi Sankyo, Esperion, Zuelling Pharma, Sanofi-Regeneron and Merck and grants from Sanofi-Regeneron and Merck.

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Schwartz, G.G., Nicholls, S.J., Toth, P.P. et al. Relation of insulin treatment for type 2 diabetes to the risk of major adverse cardiovascular events after acute coronary syndrome: an analysis of the BETonMACE randomized clinical trial. Cardiovasc Diabetol 20, 125 (2021). https://doi.org/10.1186/s12933-021-01311-9

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Keywords

  • Acute coronary syndrome
  • Diabetes
  • Epigenetics
  • BET proteins

Cardiovascular Diabetology

ISSN: 1475-2840