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肥胖与肺动脉高压:病理生理机制综述

Obesity and pulmonary hypertension: a review of pathophysiologic mechanisms.

作者信息

Friedman Scott E, Andrus Bruce W

机构信息

Section of Cardiology, Heart and Vascular Center, Dartmouth-Hitchcock Medical Center, Lebanon, NH 03756, USA ; Department of Medicine, Geisel School of Medicine at Dartmouth, Hanover, NH 03755, USA.

出版信息

J Obes. 2012;2012:505274. doi: 10.1155/2012/505274. Epub 2012 Sep 3.

Abstract

Pulmonary hypertension (PH) is a potentially life-threatening condition arising from a wide variety of pathophysiologic mechanisms. Effective treatment requires a systematic diagnostic approach to identify all reversible mechanisms. Many of these mechanisms are relevant to those afflicted with obesity. The unique mechanisms of PH in the obese include obstructive sleep apnea, obesity hypoventilation syndrome, anorexigen use, cardiomyopathy of obesity, and pulmonary thromboembolic disease. Novel mechanisms of PH in the obese include endothelial dysfunction and hyperuricemia. A wide range of effective therapies exist to mitigate the disability of PH in the obese.

摘要

肺动脉高压(PH)是一种由多种病理生理机制引起的潜在危及生命的疾病。有效的治疗需要系统的诊断方法来识别所有可逆机制。其中许多机制与肥胖患者相关。肥胖患者PH的独特机制包括阻塞性睡眠呼吸暂停、肥胖低通气综合征、食欲抑制剂的使用、肥胖性心肌病和肺血栓栓塞性疾病。肥胖患者PH的新机制包括内皮功能障碍和高尿酸血症。有多种有效的治疗方法可减轻肥胖患者PH的残疾程度。

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