Your new experience awaits. Try the new design now and help us make it even better

ORIGINAL RESEARCH article

Front. Endocrinol.

Sec. Clinical Diabetes

Plasma-derived exosomal miRNAs as potentially novel biomarkers for type 2 diabetes mellitus with abdominal obesity

Provisionally accepted
Yan  LiYan Li*Youqin  WangYouqin WangZhan  LiZhan LiLihui  FengLihui FengRu  FengRu FengJia  JiaJia JiaLi  XingLi Xing*Lu  ZhengLu Zheng*
  • Heping Hospital Affiliated to Changzhi Medical College, Changzhi, China

The final, formatted version of the article will be published soon.

Aims: To explore the plasma exosomal miRNA expression profiles in patients with abdominal obesity and type 2 diabetes mellitus (T2DM), identify differentially expressed exosomal miRNAs, and evaluate the potential of selected exosomal miRNAs as biomarkers for abdominal obesity-related T2DM. Methods: In the screening phase, high-throughput sequencing was used to detect the plasma exosomal miRNA expression profiles of non-abdominal obese individuals with normal glucose metabolism (NAO/NG, N=4), abdominal obese individuals with normal glucose metabolism (AO/NG, N=4), and abdominal obese T2DM patients (AO/T2DM, N=4). Five differentially expressed miRNAs were identified. In the independent validation phase, RT-qPCR was performed to validate the expression of these miRNAs in the NAO/NG group (N=18), AO/NG group (N=14), and AO/T2DM patients (N=17). The correlation between the miRNA levels in AO/T2DM patients and clinical features was evaluated, and the diagnostic value of the selected miRNAs for AO/T2DM was analyzed using receiver operating characteristic (ROC) curves. Results: In the screening phase, 5 exosomal miRNAs showed sequential changes among the NAO/NG, AO/NG, and AO/T2DM groups. The AO/NG group specifically expressed 16 exosomal miRNAs, while the AO/T2DM group specifically expressed 7 exosomal miRNAs. In the independent validation phase, the expression of exosomal miRNAs hsa-let-7g-5p and PC-3p-13356 in plasma increased progressively across the NAO/NG, AO/NG, and AO/T2DM groups. The expression of exosomal hsa-miR-6505-5p in the AO/T2DM group was significantly higher than that in the AO/NG and NAO/NG groups. The expression of hsa-miR-1229-3p in plasma exosomes was significantly lower in the AO/NG group compared to the NAO/NG group, but higher in the AO/T2DM group compared to the AO/NG group. No differences were detected in the expression of hsa-miR-4750-5p among the groups. The areas under the ROC curves (AUC) for plasma exosomal hsa-let-7g-5p, PC-3p-13356, and hsa-miR-6505-5p were 0.857, 0.786, and 0.878, respectively. When combined, these three miRNAs showed high diagnostic value for abdominal obesity T2DM (AUC=0.891). Conclusions: Patients with abdominal obesity and T2DM have a unique exosomal miRNA expression profiles. These characteristic exosomal miRNAs could serve as novel biomarkers for identifying such patients and may help in further understanding the pathogenesis of abdominal obesity-related T2DM.

Keywords: abdominal obesity, type 2 diabetes, exosomal, microRNA, biomarkers

Received: 29 Jun 2025; Accepted: 13 Nov 2025.

Copyright: © 2025 Li, Wang, Li, Feng, Feng, Jia, Xing and Zheng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Yan Li, liyanweiwei@126.com
Li Xing, ybhxlcbc@163.com
Lu Zheng, zhenglu0803@163.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.