Change in circulating microRNA profile of obese children indicates future risk of adult diabetes

Xianwei Cui(Nanjing Maternity and Child Health Care Hospital), Lianghui You(Nanjing Maternity and Child Health Care Hospital), Lijun Zhu(Nanjing Maternity and Child Health Care Hospital), Xing Wang(Nanjing Maternity and Child Health Care Hospital), Yahui Zhou(Nanjing Maternity and Child Health Care Hospital), Yun Li(Nanjing Maternity and Child Health Care Hospital), Juan Wen(Nanjing Maternity and Child Health Care Hospital), Yankai Xia(Nanjing Medical University), Xinru Wang(Nanjing Maternity and Child Health Care Hospital), Chenbo Ji(Nanjing Maternity and Child Health Care Hospital), Xirong Guo(Nanjing Maternity and Child Health Care Hospital)
Metabolism
September 29, 2017
Cited by 149Open Access
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Abstract

PURPOSE: Childhood obesity increases susceptibility to type 2 diabetes (T2D) in adults. Circulating microRNAs (miRNAs) in serum have been proposed as potential diagnostic biomarkers, and they may contribute to the progression toward T2D. Here, we investigated the possibility of predicting the future risk of adult T2D in obese children by using circulating miRNAs. BASIC PROCEDURES: We performed miRNA high-throughput sequencing to screen relevant circulating miRNAs in obese children. The expression patterns of targeted miRNAs were further explored in obese children and adults with T2D. To investigate the underlying contributions of these miRNAs to the development of T2D, we detected the impacts of the candidate miRNAs on preadipocyte proliferation, insulin secretion by pancreatic β-cell, and glucose uptake by skeletal muscle cells. MAIN FINDINGS: Three miRNAs (miR-486, miR-146b and miR-15b), whose expression in the circulation was most dramatically augmented in obese children and adult T2D patients, were selected for further investigation. Of these 3 miRNAs, miR-486 was implicated in accelerating preadipocyte proliferation and myotube glucose intolerance, miR-146b and miR-15b were engaged in the suppression of high concentration glucose-induced pancreatic insulin secretion, and they all contributed to the pathological processes of obesity and T2D. PRINCIPAL CONCLUSIONS: Our results provide a better understanding of the role of circulating miRNAs, particularly miR-486, miR-146b and miR-15b, in predicting the future risk of T2D in obese children.


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