AI Article Synopsis

  • Erectile dysfunction (ED) affects around 150 million people globally and may signal larger health issues like vascular diseases, particularly involving the heart and peripheral arteries.
  • The link between ED and common risk factors such as smoking, diabetes, and obesity suggests that metabolic issues significantly contribute to both ED and cardiovascular diseases.
  • While current treatments may not reverse ED completely, certain procedures like percutaneous revascularization could improve symptoms in select patients, indicating the need for further research on the male pelvic arterial structure and effective imaging techniques.

Article Abstract

Erectile dysfunction (ED) is estimated to affect 150 million people worldwide and may indicate diffuse systemic macrovascular disease. Endothelial dysfunction represents the probable pathophysiological link between vasculogenic ED, coronary artery disease (CAD), and peripheral artery disease (PAD), and the artery size hypothesis along with evidence-based research support ED as the incident clinical event. Given that many common risk factors for atherosclerosis, including smoking, diabetes mellitus, hyperlipidemia, and obesity are prevalent and causative in patients with ED, it is likely that metabolic factors play a crucial role in the link between the two disorders. The interplay of these factors provides a unifying physiological, endocrinological, and behavioral model for the association between ED, CAD, and PAD. Current therapy is unlikely to reverse the natural history of ED. Percutaneous revascularization may improve ED symptoms, and thereby quality of life, in a select group of patients. Large prospective studies are needed to define male pelvic arterial anatomy and thus enhance the utilization of internal pudendal angiography and revascularization. In this review, we provide an overview of normal erectile anatomy and physiology, the pathophysiology of ED, currently accepted diagnostic imaging modalities and treatments for ED, and recently investigated endovascular therapies for ED.

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