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肥胖、代谢综合征与骨关节炎——更新综述

Obesity, Metabolic Syndrome, and Osteoarthritis-An Updated Review.

机构信息

Department of Biotechnology, Faculty of Science & Humanities, SRM Institute of Science and Technology, Kattankulathur, Chengalpattu District, Tamil Nadu, 603203, India.

Molecular Biology Division, Indian Council of Medical Research - National Institute of Nutrition, Hyderabad, Telangana, 500007, India.

出版信息

Curr Obes Rep. 2023 Sep;12(3):308-331. doi: 10.1007/s13679-023-00520-5. Epub 2023 Aug 14.

Abstract

PURPOSE OF REVIEW

Metabolic syndrome (MetS), also called the 'deadly quartet' comprising obesity, diabetes, dyslipidemia, and hypertension, has been ascertained to have a causal role in the pathogenesis of osteoarthritis (OA). This review is aimed at discussing the current knowledge on the contribution of metabolic syndrome and its various components to OA pathogenesis and progression.

RECENT FINDINGS

Lately, an increased association identified between the various components of metabolic syndrome (obesity, diabetes, dyslipidemia, and hypertension) with OA has led to the identification of the 'metabolic phenotype' of OA. These metabolic perturbations alongside low-grade systemic inflammation have been identified to inflict detrimental effects upon multiple tissues of the joint including cartilage, bone, and synovium leading to complete joint failure in OA. Recent epidemiological and clinical findings affirm that adipokines significantly contribute to inflammation, tissue degradation, and OA pathogenesis mediated through multiple signaling pathways. OA is no longer perceived as just a 'wear and tear' disease and the involvement of the metabolic components in OA pathogenesis adds up to the complexity of the disease. Given the global surge in obesity and its allied metabolic perturbations, this review aims to throw light on the current knowledge on the pathophysiology of MetS-associated OA and the need to address MetS in the context of metabolic OA management. Better regulation of the constituent factors of MetS could be profitable in preventing MetS-associated OA. The identification of key roles for several metabolic regulators in OA pathogenesis has also opened up newer avenues in the recognition and development of novel therapeutic agents.

摘要

目的综述

代谢综合征(MetS)也被称为“致命四重奏”,包括肥胖、糖尿病、血脂异常和高血压,已被确定在骨关节炎(OA)的发病机制中起因果作用。本综述旨在讨论代谢综合征及其各种成分对 OA 发病机制和进展的贡献的最新知识。

最近的发现

最近,代谢综合征的各种成分(肥胖、糖尿病、血脂异常和高血压)与 OA 之间的关联增加,导致 OA 的“代谢表型”的确定。这些代谢紊乱以及低度全身炎症已被确定对关节的多个组织(包括软骨、骨和滑膜)造成有害影响,导致 OA 中的关节完全失效。最近的流行病学和临床发现证实,脂肪因子通过多种信号通路显著促进炎症、组织降解和 OA 发病机制。OA 不再仅仅被认为是一种“磨损”疾病,代谢成分在 OA 发病机制中的参与增加了疾病的复杂性。鉴于肥胖及其相关代谢紊乱在全球范围内的激增,本综述旨在阐明代谢综合征相关 OA 的病理生理学的最新知识,以及在代谢性 OA 管理中需要解决代谢综合征的问题。更好地调节 MetS 的组成因素可能有助于预防 MetS 相关的 OA。一些代谢调节剂在 OA 发病机制中的关键作用的确定也为 OA 发病机制的识别和新型治疗药物的开发开辟了新途径。

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