Department of Internal Medicine, Cardiovascular Division, Washington University School of Medicine, St Louis, MO 63110, USA; Department of Genetics, Washington University School of Medicine, St Louis, MO 63110, USA; McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO 63110, USA.
Department of Medicine, Division of Metabolism, Endocrinology and Nutrition, University of Washington Medicine Diabetes Institute, University of Washington School of Medicine, Seattle, WA 98109, USA.
Trends Mol Med. 2020 Aug;26(8):744-757. doi: 10.1016/j.molmed.2020.03.011. Epub 2020 May 15.
Type 1 and type 2 diabetes mellitus (T1DM and T2DM) increase the risk of atherosclerotic cardiovascular disease (CVD), resulting in acute cardiovascular events, such as heart attack and stroke. Recent clinical trials point toward new treatment and prevention strategies for cardiovascular complications of T2DM. New antidiabetic agents show unexpected cardioprotective benefits. Moreover, genetic and reverse translational strategies have revealed potential novel targets for CVD prevention in diabetes, including inhibition of apolipoprotein C3 (APOC3). Modeling and pharmacology-based approaches to improve insulin action provide additional potential strategies to combat CVD. The development of new strategies for improved diabetes and lipid control fuels hope for future prevention of CVD associated with diabetes.
1 型和 2 型糖尿病(T1DM 和 T2DM)会增加动脉粥样硬化性心血管疾病(CVD)的风险,导致急性心血管事件,如心脏病发作和中风。最近的临床试验指出了针对 T2DM 心血管并发症的新治疗和预防策略。新型抗糖尿病药物显示出意想不到的心脏保护益处。此外,遗传和反向转化策略揭示了糖尿病心血管疾病预防的潜在新靶点,包括抑制载脂蛋白 C3(APOC3)。改善胰岛素作用的建模和药理学方法为对抗 CVD 提供了额外的潜在策略。新策略的发展旨在改善糖尿病和血脂控制,为未来预防与糖尿病相关的 CVD 带来希望。