hsa-miR-1323

By Anonymous (not verified) , 13 November 2025
Disease's type
GDM
Experimental grouping
GDM(n=23),Normal Glucose Tolerance(n=46)
GPT's summary
The context of the study is that the mechanisms leading to gestational diabetes mellitus (GDM) are still under investigation, and it is unclear whether the placenta plays a role in triggering glucose intolerance or if its functions are modified in response to hyperglycemia. Circulating miRNAs are involved in placental development and function and are encapsulated in extracellular vesicles (EVs). The objective was to compare differential expression of miRNAs in circulating EVs in pregnancies complicated by GDM versus controls. This case-control study included 23 women with GDM and 46 matched controls. EV presence in early pregnancy was validated by transmission electron microscopy. Placental dimensions were assessed at 11 to 13 weeks of gestation. Differential expression of 17 miRNAs encapsulated in EVs was assessed using quantitative reverse transcription PCR. EVs were present in the early phase of placentation (6 to 15 weeks of gestation) in both cases and controls. No differences were observed for placental dimensions and estimated placental volume between GDM and control groups. Ten miRNAs showed significantly higher levels in GDM cases than in controls (P ≤ 0.05). Bioinformatics analysis showed that these miRNAs are involved in trophoblast proliferation/differentiation as well as in insulin secretion/regulation and glucose transport in pregnant women. The conclusion is that the miRNA content of blood EVs may be a promising avenue for studying the early effect of impaired glucose metabolism on placental development.
RF's name
hsa-miR-1323
Sample's type
Serum Extracellular Vesicles
Gestational weeks
6th to 15th gestational weeks
Experiemental methods
qPCR
Title
miRNA Profiles in Extracellular Vesicles From Serum Early in Pregnancies Complicated by Gestational Diabetes Mellitus
Evidence's type
Risk factor
Year
2019
Journal
Journal of Clinical Endocrinology & Metabolism (J Clin Endocrinol Metab)