The World Journal of Men's Health (Jul 2021)

COVID-19 Endothelial Dysfunction Can Cause Erectile Dysfunction: Histopathological, Immunohistochemical, and Ultrastructural Study of the Human Penis

  • Eliyahu Kresch,
  • Justin Achua,
  • Russell Saltzman,
  • Kajal Khodamoradi,
  • Himanshu Arora,
  • Emad Ibrahim,
  • Oleksandr N. Kryvenko,
  • Vania Wolff Almeida,
  • Fakiha Firdaus,
  • Joshua M. Hare,
  • Ranjith Ramasamy

DOI
https://doi.org/10.5534/wjmh.210055
Journal volume & issue
Vol. 39, no. 3
pp. 466 – 469

Abstract

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Purpose: A pilot study to describe histopathological features of penile tissue of patients who recovered from symptomatic COVID-19 infection and subsequently developed severe erectile dysfunction (ED). Materials and Methods:Materials and Methods: Penile tissue was collected from patients undergoing surgery for penile prosthesis for severe ED. Specimens were obtained from two men with a history of COVID-19 infection and two men with no history of infec-tion. Specimens were imaged with TEM and H&E staining. RT-PCR was performed from corpus cavernosum biopsies. The tissues collected were analyzed for endothelial Nitric Oxide Synthase (eNOS, a marker of endothelial function) and CO-VID-19 spike-protein expression. Endothelial progenitor cell (EPC) function was assessed from blood samples collected from COVID-19 (+) and COVID-19 (-) men. Results:Results: TEM showed extracellular viral particles ~100 nm in diameter with peplomers (spikes) near penile vascular endo-thelial cells of the COVID-19 (+) patients and absence of viral particles in controls. PCR showed presence of viral RNA in COVID-19 (+) specimens. eNOS expression in the corpus cavernosum of COVID-19 (+) men was decreased compared to COVID-19 (-) men. Mean EPC levels from the COVID-19 (+) patients were substantially lower compared to mean EPCs from men with severe ED and no history of COVID-19. Conclusions:Conclusions: Our study is the first to demonstrate the presence of the COVID-19 virus in the penis long after the initial infec-tion in humans. Our results also suggest that widespread endothelial cell dysfunction from COVID-19 infection can contrib-ute to ED. Future studies will evaluate novel molecular mechanisms of how COVID-19 infection leads to ED.

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