Table 3.
Cargo | Detection Methods | Key Points of Investigation | Model (In Vitro, In Vivo, Human) | Sample Type | Sample Size | Ref. |
---|---|---|---|---|---|---|
lncRNA, mRNA | Microarray | 84 mRNAs and 256 lncRNAs differentially expressed in EVs of GDM patients compared with controls | Human | Umbilical cord blood | 23 GDM vs 23 controls | (107) |
miRNA | RT-qPCR | miR-222-3p, miR-516b-5p, miR-16-5p, miR-517-3p and miR-518-5p | Human | Urine | 27 GDM vs 34 controls | (108) |
miRNA | RT-qPCR | miR-122-5p; miR-132-3p; miR-1323; miR-136-5p; miR-182-3p; miR-210-3p; miR-29a-3p; miR-29b-3p; miR-342-3p, and miR-520h | Human | Peripheral blood | 23 GDM vs 46 controls | (109) |
miRNA | Next generation sequencing | Differentially expressed miRNAs in EVs unveil that they target genes associated with glucose homeostasis and metabolism. | Human | Chorionic villi explant culture, skeletal muscle tissue and plasma samples | 12 GDM vs 12 controls | (110) |
circRNA | Microarray | 229 circRNAs were significantly up-regulated and 278 circRNAs were significantly down-regulated in the GDM patients | Human | Umbilical cord blood | 23 GDM vs 23 controls | (111) |
Proteins | Mass spectrometry | Ingenuity pathway analysis of the exosomal proteins revealed differential expression of the proteins targeting the sirtuin signaling pathway, oxidative phosphorylation, and mechanistic target of rapamycin signaling pathway | Human | Adipose tissue | 82 GDM vs 65 controls | (112) |
Proteins | Mass spectrometry | Bioinformatic analysis shows that the exosomal proteins in GDM target pathways are mainly associated with energy production, inflammation, and metabolism | Human | Peripheral blood | 11 GDM vs 11 controls | (113) |
Proteins | Mass spectrometry | S100 calcium binding protein A9, damage associated molecular pattern signal, was found to be significantly increased in GDM | Human | Urine | 8 GDM vs 10 controls | (114) |
lncRNA, long non-coding RNA; miRNA, microRNA; GDM, Gestational diabetes mellitus.