Level B· Emerging clinical evidence with positive signalsClinical TrialEurope PMCOpen access

The emerging role of extracellular vesicles in diabetes and complications: mechanistic insights and translational prospects

Liu S., Pan Z., Chen X., Wang Z., Zhong W., Ling J.

Clinical Trial on Chronic Kidney Disease, published in Front Endocrinol (Lausanne) (2025) — summary generated from the PubMed abstract.

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Level B· Emerging clinical evidence with positive signalsEvidence level of this study

Several human studies show positive signals, while research methods and sample sizes continue to develop.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
Read the A–D evidence level guide

This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Clinical Trial
Journal
Front Endocrinol (Lausanne) (2025)
Reported sample size
—
Source database
Europe PMC
PMID
41127521
PMCID
PMC12537412
DOI
10.3389/fendo.2025.1674028
Citations
1

Abstract (original English)

Extracellular vesicles (EVs), particularly exosomes, have emerged as key players in diabetes pathogenesis, diagnosis, and therapy. They regulate intercellular communication, influence islet function, and contribute to diabetic complications such as retinopathy, nephropathy, and cardiomyopathy. Their potential as liquid biopsy biomarkers and engineered therapeutic carriers-delivering nucleic acids, proteins, or stem cell-derived regenerative signals-offers promising avenues for diabetes management. However, there are some critical challenges in clinical translation. Future research must prioritize (1) scalable GMP-compliant production with rigorous quality control, (2) targeted delivery systems via ligand modification or biomimetic engineering, (3) improved biocompatibility through cargo optimization and stealth coatings, and (4) large-scale clinical trials to validate efficacy and safety. Addressing these hurdles is essential to harness EVs' full potential and accelerate their transition into mainstream diabetic care.

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.

Evidence level

Several human studies show positive signals, while research methods and sample sizes continue to develop.

How we grade evidence
AnimalsHumansDiabetes MellitusDiabetes ComplicationsCell CommunicationExtracellular VesiclesTranslational Research, Biomedical

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