Exploring the Molecular Link Between Diabetes and Erectile Dysfunction Through Single-Cell Transcriptome Analysis

Genes (Basel). 2024 Dec 13;15(12):1596. doi: 10.3390/genes15121596.

Abstract

Erectile dysfunction (ED) is a pathophysiological condition in which the patients cannot achieve an erection during sexual activity, and it is often overlooked yet prevalent among diabetic men, globally affecting approximately 35-75% of diabetic individuals. The precise mechanisms through which diabetes contributes to ED remain elusive, but the existing literature suggests the potential involvement of nerve and vascular damage that affects the penile supply. In the present review, we reanalyze the existing human single-cell transcriptomic data from patients having diabetes mellitus-associated ED with normal erections. The analysis validates the expression of genes associated with antioxidative pathways, growth factors, adipokines, angiogenesis, vascular functions, penile erection, sexual function, and inflammation in diverse cell types from healthy individuals and those with ED. Our transcriptomic analysis reveals alterations in the expression of adiponectin receptors in the pathogenesis of ED compared to their counterparts in healthy subjects. This comprehensive review sheds light on the molecular underpinnings of ED in the context of diabetes, providing an in-depth understanding of the biological and cellular alterations involved and paving the way for possible targeted therapeutic discoveries in the field of diabetes-associated male infertility.

Keywords: diabetes; diabetic sexual health; erectile dysfunction; human single-cell transcriptome data; men’s sexual health; microvascular complications; single-cell analysis.

Publication types

  • Review

MeSH terms

  • Diabetes Complications / genetics
  • Diabetes Complications / metabolism
  • Diabetes Mellitus / genetics
  • Diabetes Mellitus / metabolism
  • Erectile Dysfunction* / genetics
  • Erectile Dysfunction* / metabolism
  • Gene Expression Profiling
  • Humans
  • Male
  • Single-Cell Analysis*
  • Single-Cell Gene Expression Analysis
  • Transcriptome*

Grants and funding

The authors received no external funding for this research.