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肥胖介导的胰岛素抵抗的生物标志物:聚焦于微小RNA

Biomarkers of obesity-mediated insulin resistance: focus on microRNAs.

作者信息

Cai Yichen, Liu Pan, Xu Yumei, Xia Yuguo, Peng Xiaowan, Zhao Haiyan, Chen Qiu

机构信息

Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, 610072, Sichuan, China.

School of Clinical Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Diabetol Metab Syndr. 2023 Aug 4;15(1):167. doi: 10.1186/s13098-023-01137-3.

Abstract

Obesity and metabolic syndromes are becoming increasingly prevalent worldwide. Insulin resistance (IR) is a common complication of obesity. However, IR occurrence varies across individuals with obesity and may involve epigenetic factors. To rationalize the allocation of healthcare resources, biomarkers for the early risk stratification of individuals with obesity should be identified. MicroRNAs (miRNAs) are closely associated with metabolic diseases and involved in epigenetic regulation. In this review, we have summarized the changes in miRNA expression in the peripheral circulation and tissues of patients and animals with obesity-associated IR over the last 5 years and identified several candidate biomarkers that predict obesity-related IR. There are areas for improvement in existing studies. First, more than the predictive validity of a single biomarker is required, and a biomarker panel needs to be formed. Second, miRNAs are often studied in isolation and do not form a network of signaling pathways. We believe that early biomarkers can help clinicians accurately predict individuals prone to obesity-related IR at an early stage. Epigenetic regulation may be one of the underlying causes of different clinical outcomes in individuals with obesity. Future studies should focus on objectively reflecting the differences in miRNA profile expression in individuals with obesity-related IR, which may help identify more reliable biomarkers. Understanding the metabolic pathways of these miRNAs can help design new metabolic risk prevention and management strategies, and support the development of drugs to treat obesity and metabolic disorders.

摘要

肥胖和代谢综合征在全球范围内正变得越来越普遍。胰岛素抵抗(IR)是肥胖的常见并发症。然而,IR的发生在肥胖个体中存在差异,可能涉及表观遗传因素。为了合理分配医疗资源,应确定肥胖个体早期风险分层的生物标志物。微小RNA(miRNA)与代谢性疾病密切相关,并参与表观遗传调控。在本综述中,我们总结了过去5年肥胖相关IR患者和动物外周循环及组织中miRNA表达的变化,并确定了几种预测肥胖相关IR的候选生物标志物。现有研究仍有改进空间。首先,需要的不仅仅是单一生物标志物的预测有效性,还需要形成一个生物标志物组合。其次,miRNA通常是单独研究的,没有形成信号通路网络。我们认为早期生物标志物可以帮助临床医生在早期准确预测易患肥胖相关IR的个体。表观遗传调控可能是肥胖个体不同临床结局的潜在原因之一。未来的研究应专注于客观反映肥胖相关IR个体中miRNA谱表达的差异,这可能有助于识别更可靠的生物标志物。了解这些miRNA的代谢途径有助于设计新的代谢风险预防和管理策略,并支持治疗肥胖和代谢紊乱药物的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/918f/10401761/3e966ccc68f3/13098_2023_1137_Fig1_HTML.jpg

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