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Effect of aspirin on platelet-rich plasma of diabetes mellitus with lower extremity atherosclerosis. | LitMetric

AI Article Synopsis

  • Platelet-rich plasma (PRP) is being studied as a potential treatment for diabetic foot ulcers (DFUs), but the impact of aspirin on its growth factor content is still unclear.
  • The study compared PRP from diabetic patients taking aspirin with those not taking it, and found that both had lower growth factor levels than a control group of healthy volunteers.
  • Results showed that while aspirin use does not hinder PRP therapy, PRP from healthy individuals is more effective for enhancing the healing of DFUs compared to that from diabetic patients.

Article Abstract

Platelet-rich plasma (PRP), enriched with multiple growth factors, is a promising adjunctive therapy for diabetic foot ulcers (DFUs). As a classic anti-platelet drug for diabetic patients, the effects of aspirin on the content of growth factors in PRP remains unclear. Our study enrolled diabetic patients who were currently taking or not taking aspirin as the research subjects, with healthy volunteers as the control. PRP from these individuals was activated with glucose calcium and thrombin. Growth factors levels in PRP activated supernatant (PRP-AS) and wound healing ability of platelet gel (PG) in the full-thickness skin defect diabetic mouse model were compared. We found the level of growth factors in PRP-AS derived from two groups of diabetic patients were not statistically different, whereas both lower than that from healthy volunteers. Similarly, we found better wound healing ability of PG from healthy volunteers than those from diabetic patients, but no difference between the two groups of diabetic patients in the mouse model. Aspirin does not interfere with autologous PRP therapy when using calcium gluconate and thrombin as agonists. However considering the content of growth factors, PRP from healthy volunteers is a preferable option for promoting DFU repair.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11508953PMC
http://dx.doi.org/10.1080/20565623.2024.2413827DOI Listing

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