Key result
The combination of circulating miRNA-223 and ANGPTL8 demonstrated high diagnostic accuracy for gestational diabetes mellitus, with an AUC of 0.97 (95% CI 0.95-0.99).
Why the study?
New biomarkers capable of predicting or aiding in the early diagnosis of gestational diabetes mellitus are needed to minimize hyperglycaemia-related complications for pregnant women and their offspring.
Are circulating miRNA-223 and ANGPTL8 levels associated with gestational diabetes mellitus in pregnant women?
Case-Control (n=212)
Are circulating miRNA-223 and ANGPTL8 levels associated with gestational diabetes mellitus in pregnant women?
Effect estimate: AUC 0.97 (95% CI 0.95-0.99)
Circulating miRNA-223 and ANGPTL8 are significantly elevated in gestational diabetes mellitus and show high diagnostic accuracy, suggesting their potential as biomarkers for early diagnosis.
Supports biomarker evaluation for gestational diabetes; hypothesis-generating from case-control data and should not yet change practice.
BSTRACTBackground Gestational diabetes mellitus (GDM) is a serious health problem associated with both foetal and maternal complications. New biomarkers that can predict or help in the early diagnosis of GDM are needed to minimize the hazards of hyperglycaemia in pregnant women and their offspring. We hypothesised a link between levels of microRNA-223 (miRNA-223) and Angiopoietin-Like Protein 8 (ANGPTL8) and GDM.Materials and Methods The study included 109 patients with confirmed early diagnosed GDM and 103 healthy control pregnant women in their second or third trimester. miRNA-223 and ANGPTL8 blood levels were assessed by real-time RT-PCR and sandwich ELISA, respectively, laboratory markers by standard methods.Results There was a significant increase in mean [SD] miRNA-223 and ANGPTL8 in GDM (0.31 [0.06] relative units) and (692 [199] pg/ml), respectively, in the GDM women compared to healthy pregnant women (0.17[0.05] relative units) and (261 [127] pg/ml), respectively, P < 0.001. miRNA-223 and ANGPTL8 correlated significantly with each other (r = 0.38, P < 0.001) and with fasting, 1-h and 2-h postprandial blood glucose levels (all P ≤ 0.002) HbA1 c (P < 0.025), total cholesterol (P < 0.01), LDL-C and triglycerides (both P ≤ 0.005). The ROC area under curve (AUC) (95%CI) was 0.94 (0.91–0.97) for ANGPTL8, 0.92 (0.88–0.96) for miRNA-223 and 0.97 (0.95 − 0.99) for their combination.Conclusions These findings support the hypothesis of involvement of both miRNA-223 and ANGPTL8 in the pathogenesis of GDM. The difference between levels in GDM patients and in control pregnant women indicates potential use for early diagnosis or prediction of GDM.
No takes yet. Share an insight, caveat, or question.
Abdeltawab et al. (2020) conducted a case-control in Gestational diabetes mellitus (n=212). Circulating miRNA-223 and ANGPTL8 vs. Healthy pregnant women was evaluated on Diagnostic accuracy (ROC AUC) of combined miRNA-223 and ANGPTL8 (AUC 0.97, 95% CI 0.95-0.99). The combination of circulating miRNA-223 and ANGPTL8 demonstrated high diagnostic accuracy for gestational diabetes mellitus, with an AUC of 0.97 (95% CI 0.95-0.99).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: