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代谢综合征中内皮功能障碍的机制。

Mechanisms of endothelial dysfunction in the metabolic syndrome.

作者信息

Deedwania Prakash C

机构信息

Division of Cardiology, Department of Medicine, VA Central California Health Care System and University of California at San Francisco Program, 2615 East Clinton Avenue (111), Fresno, CA 93703, USA.

出版信息

Curr Diab Rep. 2003 Aug;3(4):289-92. doi: 10.1007/s11892-003-0019-8.

Abstract

Cardiovascular disease is a leading cause of death and disability in patients with diabetes or metabolic syndrome (MS). The available data suggest that many patients with diabetes or MS already have vascular abnormalities by the time they are diagnosed with their metabolic disorder. Endothelial dysfunction (ED), which is one of the initial steps in the process of vascular disease, is often present in patients with diabetes or MS. Although the precise mechanism(s) by which diabetes or MS causes ED remains to be elucidated, several possibilities exist. Hyperglycemia, hyperinsulinemia, increased oxidative stress, and diabetic dyslipidemia can all contribute to ED individually or in concert with one another. ED in the setting of diabetes or MS can subsequently result in the activation of a variety of pathways that alter vascular function and participate in the process of vascular remodeling and atherosclerosis. Because insulin resistance is the predominant mechanism responsible for various perturbations seen in MS or diabetes, it is essential to develop a therapeutic strategy that can improve insulin sensitivity with the hope that such interventions would reduce the risk of future cardiovascular events.

摘要

心血管疾病是糖尿病或代谢综合征(MS)患者死亡和残疾的主要原因。现有数据表明,许多糖尿病或MS患者在被诊断出患有代谢紊乱时就已经存在血管异常。内皮功能障碍(ED)是血管疾病过程中的初始步骤之一,在糖尿病或MS患者中经常存在。尽管糖尿病或MS导致ED的确切机制仍有待阐明,但存在几种可能性。高血糖、高胰岛素血症、氧化应激增加和糖尿病血脂异常都可能单独或相互协同导致ED。糖尿病或MS背景下的ED随后可导致多种途径的激活,这些途径会改变血管功能并参与血管重塑和动脉粥样硬化过程。由于胰岛素抵抗是MS或糖尿病中各种紊乱的主要机制,因此制定一种能够提高胰岛素敏感性的治疗策略至关重要,希望此类干预措施能够降低未来心血管事件的风险。

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