Circulating microRNA Related to Cardiometabolic Risk Factors for Metabolic Syndrome: A Systematic Review

被引:7
作者
Brandao-Lima, Paula N. [1 ]
de Carvalho, Gabrielli B. [1 ]
Payolla, Tanyara B. [1 ]
Sarti, Flavia M. [2 ]
Rogero, Marcelo M. [1 ]
机构
[1] Univ Sao Paulo, Sch Publ Hlth, Dept Nutr, 715 Dr Arnaldo Ave, BR-01246904 Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, Sch Arts, Sci & Humanities, 1000 Arlindo Bettio Ave, BR-03828000 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
miRNA; serum; plasma; obesity; type; 2; diabetes; metabolic syndrome; INSULIN-RESISTANCE; OBESITY; SERUM; INFLAMMATION; EXPRESSION; ATHEROSCLEROSIS; IDENTIFICATION; ASSOCIATION; BIOMARKERS; CHILDREN;
D O I
10.3390/metabo12111044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNA regulates multiple pathways in inflammatory response, adipogenesis, and glucose and lipid metabolism, which are involved in metabolic syndrome (MetS). Thus, this systematic review aimed at synthesizing the evidence on the relationships between circulating microRNA and risk factors for MetS. The systematic review was registered in the PROSPERO database (CRD42020168100) and included 24 case-control studies evaluating microRNA expression in serum/plasma of individuals >= 5 years old. Most of the studies focused on 13 microRNAs with higher frequency and there were robust connections between miR-146a and miR-122 with risk factors for MetS, based on average weighted degree. In addition, there was an association of miR-222 with adiposity, lipid metabolism, glycemic metabolism, and chronic inflammation and an association of miR-126, miR-221, and miR-423 with adiposity, lipid, and glycemic metabolism. A major part of circulating microRNA was upregulated in individuals with risk factors for MetS, showing correlations with glycemic and lipid markers and body adiposity. Circulating microRNA showed distinct expression profiles according to the clinical condition of individuals, being particularly linked with increased body fat. However, the exploration of factors associated with variations in microRNA expression was limited by the variety of microRNAs investigated by risk factor in diverse studies identified in this systematic review.
引用
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页数:22
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