Circulating microRNAs Showed Specific Responses according to Metabolic Syndrome Components and Sex of Adults from a Population-Based Study
Paula N. Brandão-Lima,
Gabrielli B. de Carvalho,
Tanyara B. Payolla,
Flávia M. Sarti,
Regina M. Fisberg,
Fiona C. Malcomson,
John C. Mathers,
Marcelo M. Rogero
Affiliations
Paula N. Brandão-Lima
Department of Nutrition, School of Public Health, University of São Paulo, 715 Dr. Arnaldo Avenue, Pacaembu 01246-904, Brazil
Gabrielli B. de Carvalho
Department of Nutrition, School of Public Health, University of São Paulo, 715 Dr. Arnaldo Avenue, Pacaembu 01246-904, Brazil
Tanyara B. Payolla
Department of Nutrition, School of Public Health, University of São Paulo, 715 Dr. Arnaldo Avenue, Pacaembu 01246-904, Brazil
Flávia M. Sarti
School of Arts, Sciences and Humanities, University of São Paulo, 1000 Arlindo Bettio Avenue, Sao Paulo 03828-000, Brazil
Regina M. Fisberg
Department of Nutrition, School of Public Health, University of São Paulo, 715 Dr. Arnaldo Avenue, Pacaembu 01246-904, Brazil
Fiona C. Malcomson
Human Nutrition & Exercise Research Centre, Centre for Healthier Lives, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK
John C. Mathers
Human Nutrition & Exercise Research Centre, Centre for Healthier Lives, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK
Marcelo M. Rogero
Department of Nutrition, School of Public Health, University of São Paulo, 715 Dr. Arnaldo Avenue, Pacaembu 01246-904, Brazil
MicroRNAs (miRNAs) regulate several metabolic pathways and are potential biomarkers for early risk prediction of metabolic syndrome (MetS). Our aim was to evaluate the levels of 21 miRNAs in plasma according to MetS components and sex in adults. We employed a cross-sectional study of 192 adults aged 20 to 59 years old from the 2015 Health Survey of São Paulo with Focus in Nutrition. Data showed reduced levels of miR-16 and miR-363 in women with MetS; however, men with one or more risk factors showed higher levels of miR-let-7c and miR-30a. Individuals with raised waist circumference showed higher levels of miR-let-7c, miR-122, miR-30a, miR-146a, miR-15a, miR-30d and miR-222. Individuals with raised blood pressure had higher miR-30a, miR-122 and miR-30a levels. Plasma levels of four miRNAs (miR-16, miR-363, miR-375 and miR-486) were lower in individuals with low HDL-cholesterol concentrations. In addition, plasma levels of five miRNAs (miR-122, miR-139, miR-let-7c, miR-126 and miR-30a) were increased in individuals with high fasting plasma glucose and/or insulin resistance. Our results suggest that the pattern of miRNA levels in plasma may be a useful early biomarker of cardiometabolic components of MetS and highlight the sex differences in the plasma levels of miRNAs in individuals with MetS.