Sex Differences in Genomic Drivers of Adipose Distribution and Related Cardiometabolic Disorders: Opportunities for Precision Medicine.

H. Lumish, M. O'Reilly, M. Reilly
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引用次数: 39

Abstract

This review focuses on the human genetics, epidemiology, and molecular pathophysiology of sex differences in central obesity, adipose distribution, and related cardiometabolic disorders. Distribution of fat is important for cardiometabolic health, with peripheral fat depots having a protective effect and central visceral fat depots conferring a detrimental effect on health. There are important sex differences in fat distribution that are masked when studying body mass index as a measure of obesity. From epidemiological, murine, and in vitro studies, several mechanisms have been proposed to explain the sex differences in adipose distribution, including sex hormonal effects, cell-intrinsic properties, and the microenvironment in fat depots. More recently, human genetics have revealed hundreds of loci for central obesity providing disruptive opportunities for mechanistic discoveries and clinical translation. A striking feature is that over one-third of these loci have reproducible but poorly understood sexual dimorphic associations with central obesity, most having stronger effects in women. Understanding the genetic and molecular mechanisms of adipose distribution and its sexual dimorphism in humans provides a unique opportunity to advance mechanism-based, sex and gender aware, precision medicine for early identification of at-risk individuals, as well as novel therapeutic strategies for central obesity and cardiometabolic disorders.
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脂肪分布和相关心脏代谢疾病的基因组驱动因素的性别差异:精准医学的机会。
本文综述了人类遗传学、流行病学和中枢性肥胖、脂肪分布和相关心脏代谢疾病的性别差异的分子病理生理学。脂肪的分布对心脏代谢健康很重要,外周脂肪库具有保护作用,而中央内脏脂肪库对健康有不利影响。在研究体重指数作为肥胖的衡量标准时,脂肪分布的重要性别差异被掩盖了。从流行病学、小鼠和体外研究中,已经提出了几种机制来解释脂肪分布的性别差异,包括性激素效应、细胞内在特性和脂肪库的微环境。最近,人类遗传学揭示了数百个中心性肥胖的基因座,为机制发现和临床转化提供了破坏性的机会。一个显著的特征是,超过三分之一的这些基因座与中心性肥胖具有可重复的但鲜为人知的两性二态关联,其中大多数对女性有更强的影响。了解人类脂肪分布及其性别二态性的遗传和分子机制,为推进基于机制的、性别和性别意识的精准医学提供了一个独特的机会,可以早期识别高危个体,以及为中枢性肥胖和心脏代谢疾病提供新的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Editors and Editorial Board. Correction to: Role of LpL (Lipoprotein Lipase) in Macrophage Polarization In Vitro and In Vivo. Tribute to Paul M. Vanhoutte, MD, PhD (1940-2019). Correction to: 18F-Sodium Fluoride Imaging of Coronary Atherosclerosis in Ambulatory Patients With Diabetes Mellitus. Extracellular MicroRNA-92a Mediates Endothelial Cell-Macrophage Communication.
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