Central Obesity and Insulin Resistance in the Cardiometabolic Syndrome: Pathways to Preclinical Cardiovascular Structure and Function

Johanna R. Klaus PhD, Barry E. Hurwitz PhD, Maria M. Llabre PhD,  Jay S. Skyler MD, Ronald B. Goldberg MD, Jennifer B. Marks MD,  Martin S. Bilsker MD, Neil Schneiderman PhD
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引用次数: 27

Abstract

The cardiometabolic syndrome (CMS) has been an organizing conceptual framework for subclinical cardiovascular pathophysiology. Using cross-sectional data from 338 healthy men and women aged 18 to 55 years, the study examined the role of central adiposity and insulin sensitivity and assessed potential relationships with other metabolic indices (insulin sensitivity, glucose tolerance, fibrinolysis, lipidemia, endothelial function, and inflammation) and measures of cardiac structure and function (cardiac mass, compliance and contractility, myocardial oxygen demand, and blood pressure). Structural equation modeling analyses, which controlled for sex, age, and race, demonstrated good fit to the data. The derived relationships provided a physiologically consistent model of CMS, with an initiating role for central adiposity and insulin resistance. The model accounted for 30% and 82% of the variance in diastolic blood pressure and myocardial oxygen demand, respectively. The findings suggest predominant pathways through which subclinical metabolic processes may exert pathogenic impact on the heart and vasculature.

中心肥胖和胰岛素抵抗在心脏代谢综合征:途径到临床前心血管结构和功能
心血管代谢综合征(CMS)已成为亚临床心血管病理生理学的组织概念框架。利用338名年龄在18至55岁之间的健康男性和女性的横断面数据,该研究检查了中心性肥胖和胰岛素敏感性的作用,并评估了与其他代谢指标(胰岛素敏感性、葡萄糖耐量、纤维蛋白溶解、血脂、内皮功能和炎症)和心脏结构和功能测量(心脏质量、顺应性和收缩性、心肌需氧量和血压)的潜在关系。结构方程模型分析,控制性别,年龄和种族,证明了良好的拟合数据。推导出的关系提供了一个生理上一致的CMS模型,具有中心肥胖和胰岛素抵抗的初始作用。该模型分别解释了舒张压和心肌需氧量差异的30%和82%。研究结果表明,亚临床代谢过程可能通过主要途径对心脏和血管系统产生致病影响。
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