Prevention of cardiovascular disease in women with type 2 diabetes: the role of incretin mimetics and sodium-glucose cotransporter-2 inhibitors.

IF 4.7 2区 生物学 Q2 CELL BIOLOGY American journal of physiology. Cell physiology Pub Date : 2025-01-01 Epub Date: 2024-12-13 DOI:10.1152/ajpcell.00765.2024
Eiman Ibrahim, Mya Burken, Guido Lastra, Camila Manrique-Acevedo
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Abstract

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.

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预防女性 2 型糖尿病患者的心血管疾病:诱导素模拟物和葡萄糖钠转运体-2抑制剂的作用
心血管疾病(CVD)是2型糖尿病(T2D)患者死亡的主要原因,与男性相比,女性经历的事件风险不成比例。一旦确诊为T2D,女性的心血管风险因素负担就会增加。肠促胰岛素模拟物现在通过改善血糖控制、促进体重减轻和潜在的直接心脏保护作用,在管理心血管风险方面发挥着核心作用。同样,钠-葡萄糖共转运蛋白2抑制剂通过各种非降糖机制有助于预防CVD。这两类药物都是个性化治疗策略的组成部分,旨在解决女性糖尿病患者面临的心血管风险增加。这篇小型综述探讨了心血管风险增加的可能机制,并探讨了促肠促胰岛素模拟物和SGLT2抑制剂在缓解女性T2D心血管疾病中的作用。在糖尿病护理中强调个性化和性别特异性方法对于优化治疗结果和改善心血管健康至关重要。
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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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