Ibrahim Eiman, Burken Mya, Lastra Guido, Manrique-Acevedo Camila
Division of Endocrinology and Metabolism, Department of Medicine, University of Missouri, Columbia, Missouri, United States.
Harry S. Truman Memorial Veterans' Hospital, Columbia, Missouri, United States.
Am J Physiol Cell Physiol. 2025 Jan 1;328(1):C315-C322. doi: 10.1152/ajpcell.00765.2024. Epub 2024 Dec 13.
Cardiovascular disease (CVD) is the leading cause of death among individuals with type 2 diabetes (T2D), with women experiencing a disproportionate risk of events compared with men. Women have an amplified burden of cardiovascular risk factors once T2D is diagnosed. Incretin mimetics now plays a central role in managing cardiovascular risk by improving glycemic control, promoting weight loss, and potentially exerting direct cardioprotective effects. Similarly, sodium-glucose cotransporter-2 inhibitors contribute to CVD prevention through various nonglucose-lowering mechanisms. Both classes of medications are integral to personalized treatment strategies aimed at addressing the heightened cardiovascular risk faced by women with diabetes. This mini-review addresses possible mechanisms underlying the increased cardiovascular risk and explores the role of incretin mimetics and SGLT2 inhibitors in mitigating CVD in women with T2D. Emphasizing personalized and sex-specific approaches in diabetes care is crucial for optimizing treatment outcomes and improving cardiovascular health.
心血管疾病(CVD)是2型糖尿病(T2D)患者的主要死因,与男性相比,女性发生心血管事件的风险更高。一旦确诊T2D,女性心血管危险因素的负担就会加重。肠促胰岛素类似物现在通过改善血糖控制、促进体重减轻以及可能发挥直接的心脏保护作用,在管理心血管风险方面发挥着核心作用。同样,钠-葡萄糖协同转运蛋白2抑制剂通过各种非降糖机制有助于预防CVD。这两类药物都是旨在解决糖尿病女性面临的心血管风险增加问题的个性化治疗策略的组成部分。本综述探讨了心血管风险增加的潜在机制,并探讨了肠促胰岛素类似物和SGLT2抑制剂在减轻T2D女性心血管疾病方面的作用。强调糖尿病护理中的个性化和性别特异性方法对于优化治疗效果和改善心血管健康至关重要。