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多囊卵巢综合征中的代谢组学生物标志物:证据综述

Metabolomic Biomarkers in Polycystic Ovary Syndrome: A Review of the Evidence.

作者信息

Alesi Simon, Ghelani Drishti, Mousa Aya

机构信息

Monash Centre for Health Research and Implementation (MCHRI), School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.

出版信息

Semin Reprod Med. 2021 Jul;39(3-04):102-110. doi: 10.1055/s-0041-1729841. Epub 2021 May 4.

Abstract

Polycystic ovary syndrome (PCOS) is an endocrinologic condition affecting one in five women of reproductive age. PCOS is often characterized by disruptions to the menstrual cycle, development of male-pattern hair growth (hirsutism), and polycystic ovary morphology. Recently, PCOS has been linked to metabolic dysfunction, with 40 to 80% of women characterized as overweight or obese. Despite these well-known negative health effects of PCOS, 75% of sufferers remain undiagnosed. This is most likely due to the variability in symptom presentation and the lack of a definitive test for the condition. Metabolomics, which is a platform used to analyze and characterize a large number of metabolites, has recently been proposed as a potential tool for investigating the metabolic pathways that could be involved in the pathophysiology of PCOS. In doing so, novel biomarkers could be identified to improve diagnosis and treatment of PCOS. This review aims to summarize the findings of recent metabolomic studies that highlight metabolic-specific molecules which are deranged in PCOS, to identify potential biomarkers for the condition. Current limitations for metabolomic studies are discussed, as well as future directions to progress the field toward further validation and integration into clinical practice.

摘要

多囊卵巢综合征(PCOS)是一种影响五分之一育龄女性的内分泌疾病。PCOS的特征通常是月经周期紊乱、出现男性型毛发增多(多毛症)以及多囊卵巢形态。最近,PCOS与代谢功能障碍有关,40%至80%的女性被归类为超重或肥胖。尽管PCOS有这些众所周知的负面健康影响,但75%的患者仍未被诊断出来。这很可能是由于症状表现的变异性以及缺乏针对该疾病的确定性检测方法。代谢组学是一个用于分析和表征大量代谢物的平台,最近已被提议作为一种潜在工具,用于研究可能参与PCOS病理生理学的代谢途径。通过这样做,可以识别出新的生物标志物,以改善PCOS的诊断和治疗。本综述旨在总结近期代谢组学研究的结果,这些研究突出了在PCOS中紊乱的代谢特异性分子,以确定该疾病的潜在生物标志物。讨论了代谢组学研究的当前局限性,以及该领域朝着进一步验证并整合到临床实践发展的未来方向。

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