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胰岛素抵抗与内皮

Insulin resistance and the endothelium.

作者信息

Quiñones Manuel J, Nicholas Susanne B, Lyon Christopher J

机构信息

David Geffen School of Medicine at UCLA, University of California Los Angeles, Los Angeles, CA 90095, USA.

出版信息

Curr Diab Rep. 2005 Aug;5(4):246-53. doi: 10.1007/s11892-005-0018-z.

Abstract

Type 2 diabetes is a cardiovascular disease equivalent that is associated with accelerated atherosclerosis and significant mortality. However, the metabolic syndrome and prediabetes are associated with increased cardiovascular mortality, indicating that atherogenic vascular changes begin prior to the onset of overt diabetes. At the core of diabetes and the metabolic syndrome is insulin resistance (IR), which sets the stage for dyslipidemia, hypertension, and inflammation. Endothelial dysfunction is the first stage of the atherosclerosis process and results from exposure to cardiovascular risk factors, such as IR and diabetes. IR and atherosclerosis follow parallel paths as they progress in severity. Thiazolidinediones, angiotensin-converting enzyme inhibitors, angiotensin receptor-AT1 blockers, and statins are widely used in the treatment of diabetes. Emerging evidence indicates that these pharmacologic agents have added mechanisms of action, especially on the endothelium and in the prevention of diabetes.

摘要

2型糖尿病是一种等同于心血管疾病的病症,与动脉粥样硬化加速和显著死亡率相关。然而,代谢综合征和糖尿病前期与心血管死亡率增加相关,表明致动脉粥样硬化的血管变化在显性糖尿病发作之前就已开始。糖尿病和代谢综合征的核心是胰岛素抵抗(IR),它为血脂异常、高血压和炎症奠定了基础。内皮功能障碍是动脉粥样硬化过程的第一阶段,由暴露于心血管危险因素如IR和糖尿病引起。IR和动脉粥样硬化在严重程度进展过程中呈平行发展态势。噻唑烷二酮类、血管紧张素转换酶抑制剂、血管紧张素受体AT1阻滞剂和他汀类药物广泛用于糖尿病治疗。新出现的证据表明,这些药物具有额外的作用机制,尤其是对内皮以及在预防糖尿病方面。

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