AI Article Synopsis

  • Peripheral arterial disease (PAD) is increasingly common due to factors like obesity, diabetes, aging, and smoking, with chronic limb-threatening ischemia (CLTI) being its most severe form.
  • Revascularization is the main treatment for CLTI, but many patients aren’t suitable candidates, leading to a need for alternative therapies.
  • The review focuses on the epigenetic mechanisms behind angiogenesis in PAD, specifically the role of long non-coding RNAs and fibroblast-endothelial cell interactions, while exploring new treatment possibilities that could arise from understanding these processes.

Article Abstract

Peripheral arterial disease (PAD) represents a global health concern with a rising prevalence attributed to factors such as obesity, diabetes, aging, and smoking. Among patients with PAD, chronic limb-threatening ischemia (CLTI) is the most severe manifestation, associated with substantial morbidity and mortality. While revascularization remains the primary therapy for CLTI, not all patients are candidates for such interventions, highlighting the need for alternative approaches. Impaired angiogenesis, the growth of new blood vessels, is a central feature of PAD, and despite decades of research, effective clinical treatments remain elusive. Epigenetics, the study of heritable changes in gene expression, has gained prominence in understanding PAD pathogenesis. Here, we explore the role of epigenetic regulation in angiogenesis within the context of PAD, with a focus on long non-coding RNAs and fibroblast-endothelial cell transdifferentiation. Additionally, we discuss the interplay between metabolic control and epigenetic regulation, providing insights into potential novel therapeutic avenues for improving PAD treatments. This review aims to offer a concise update on the application of epigenetics in angiogenesis and PAD research, inspiring further investigations in this promising field.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655766PMC
http://dx.doi.org/10.14797/mdcvj.1294DOI Listing

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