Obesity, insulin resistance and comorbidities? Mechanisms of association.

Ana Valeria B Castro, Cathryn M Kolka, Stella P Kim, Richard N Bergman
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引用次数: 196

Abstract

Overall excess of fat, usually defined by the body mass index, is associated with metabolic (e.g. glucose intolerance, type 2 diabetes mellitus (T2DM), dyslipidemia) and non-metabolic disorders (e.g. neoplasias, polycystic ovary syndrome, non-alcoholic fat liver disease, glomerulopathy, bone fragility etc.). However, more than its total amount, the distribution of adipose tissue throughout the body is a better predictor of the risk to the development of those disorders. Fat accumulation in the abdominal area and in non-adipose tissue (ectopic fat), for example, is associated with increased risk to develop metabolic and non-metabolic derangements. On the other hand, observations suggest that individuals who present peripheral adiposity, characterized by large hip and thigh circumferences, have better glucose tolerance, reduced incidence of T2DM and of metabolic syndrome. Insulin resistance (IR) is one of the main culprits in the association between obesity, particularly visceral, and metabolic as well as non-metabolic diseases. In this review we will highlight the current pathophysiological and molecular mechanisms possibly involved in the link between increased VAT, ectopic fat, IR and comorbidities. We will also provide some insights in the identification of these abnormalities.

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肥胖、胰岛素抵抗和合并症?联想机制。
脂肪总体过量,通常由体重指数定义,与代谢性疾病(如葡萄糖耐受不良、2型糖尿病、血脂异常)和非代谢性疾病(如肿瘤、多囊卵巢综合征、非酒精性脂肪性肝病、肾小球病、骨质疏松等)有关。然而,脂肪组织在全身的分布比其总量更能预测这些疾病发展的风险。例如,腹部和非脂肪组织(异位脂肪)的脂肪积累与发生代谢和非代谢紊乱的风险增加有关。另一方面,观察结果表明,以臀部和大腿围围大为特征的外周性肥胖个体具有更好的葡萄糖耐量,降低了T2DM和代谢综合征的发病率。胰岛素抵抗(IR)是肥胖(尤其是内脏疾病)与代谢性和非代谢性疾病之间关联的主要罪魁祸首之一。在这篇综述中,我们将重点介绍VAT增加、异位脂肪、IR和合并症之间可能涉及的当前病理生理和分子机制。我们还将提供一些识别这些异常的见解。
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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