Early Second-Trimester Serum MiRNA Profiling Predicts Gestational Diabetes Mellitus

Chun Zhao(Nanjing Maternity and Child Health Care Hospital), Jing Dong(Nanjing Medical University), Tao Jiang(Nanjing Maternity and Child Health Care Hospital), Zhonghua Shi(Nanjing Maternity and Child Health Care Hospital), Bin Yu, Yun‐Long Zhu, Daozhen Chen, XU Jun-rong(Jiangsu Province Hospital), Ran Huo(Nanjing Medical University), Juncheng Dai(Nanjing Medical University), Yankai Xia(Nanjing Medical University), Shiyang Pan(Jiangsu Province Hospital), Zhibin Hu(Nanjing Medical University), Jiahao Sha(Nanjing Medical University)
PLoS ONE
August 24, 2011
Cited by 229Open Access
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Abstract

BACKGROUND: Gestational diabetes mellitus (GDM) is one type of diabetes that presents during pregnancy and significantly increases the risk of a number of adverse consequences for the fetus and mother. The microRNAs (miRNA) have recently been demonstrated to abundantly and stably exist in serum and to be potentially disease-specific. However, no reported study investigates the associations between serum miRNA and GDM. METHODOLOGY/PRINCIPAL FINDINGS: We systematically used the TaqMan Low Density Array followed by individual quantitative reverse transcription polymerase chain reaction assays to screen miRNAs in serum collected at 16-19 gestational weeks. The expression levels of three miRNAs (miR-132, miR-29a and miR-222) were significantly decreased in GDM women with respect to the controls in similar gestational weeks in our discovery evaluation and internal validation, and two miRNAs (miR-29a and miR-222) were also consistently validated in two-centric external validation sample sets. In addition, the knockdown of miR-29a could increase Insulin-induced gene 1 (Insig1) expression level and subsequently the level of Phosphoenolpyruvate Carboxy Kinase2 (PCK2) in HepG2 cell lines. CONCLUSIONS/SIGNIFICANCE: Serum miRNAs are differentially expressed between GDM women and controls and could be candidate biomarkers for predicting GDM. The utility of miR-29a, miR-222 and miR-132 as serum-based non-invasive biomarkers warrants further evaluation and optimization.


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