Sex differences in the complications, care and clinical outcomes of patients with type 2 diabetes in the Exenatide Study of Cardiovascular Event Lowering (EXSCEL)

Author:

Green Jennifer B.1ORCID,Merrill Peter1,Lokhnygina Yuliya1,Mentz Robert J.1,Alfredsson Joakim2,Holman Rury R.3,

Affiliation:

1. Duke Clinical Research Institute, Duke University School of Medicine Durham North Carolina USA

2. Department of Cardiology and Department of Health, Medicine and Caring Sciences Linköping University Linköping Sweden

3. Diabetes Trials Unit, Radcliffe Department of Medicine University of Oxford Oxford UK

Abstract

AbstractAimTo examine sex differences in the characteristics and outcomes in participants with type 2 diabetes (T2D), with or without cardiovascular disease (CVD), randomized to once‐weekly exenatide (EQW) or placebo in the Exenatide Study of Cardiovascular Event Lowering (EXSCEL).Materials and MethodsBaseline characteristics were summarized and compared by sex. Cox proportional hazards regression models were used for clinical outcomes, including the primary composite outcome of cardiovascular (CV) death, non‐fatal myocardial infarction or non‐fatal stroke (MACE3). Models including sex‐by‐treatment interaction were used to evaluate differences in effects of EQW.ResultsOverall, 5603 women and 9149 men were followed for a median of 3.2 years. Women were younger (mean 61.4 vs. 62.2 years, P < .001) and had a shorter duration of diabetes (mean 12.9 vs. 13.2 years, P = .039) and less coronary artery disease (35.2% vs. 61.0%, P < .001) than men, but also a less favourable metabolic risk profile and lower use of cardioprotective medications. MACE3 occurred in 9.1% of women and 13.5% of men, corresponding to 2.82 versus 4.40 events/100 participant‐years (adjusted hazard ratio 0.80, 95% CI: 0.70‐0.93, P = .003). There was no difference in MACE3 with EQW compared with placebo, or evidence of heterogeneity of treatment effect by sex.ConclusionsThis analysis of a large population of individuals with T2D, with or without established CVD, identified between‐sex differences in clinical characteristics and care. Despite having worse management of CV risk factors, women had significantly lower rates of important CV events not attributable to the effects of study treatment.

Funder

Amylin Pharmaceuticals

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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