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Erectile dysfunction in diabetes mellitus : a comprehensive narrative review of pathophysiology, genetic association studies and therapeutic approaches
ID Hostnik, Boštjan (Author), ID Tonin, Gašper (Author), ID Janež, Andrej (Author), ID Klen, Jasna (Author)

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Abstract
Introduction Erectile dysfunction (ED) is a highly prevalent complication of diabetes mellitus (DM), significantly impairing quality of life and psychosocial well-being. The prevalence of ED is estimated to be over 3.5 times higher in men with diabetes mellitus compared to those without. The aetiology of diabetic ED is multifactorial, stemming from complex diabetes mellitus-related systemic changes. The pathophysiology of diabetic ED involves interacting pathways, including endothelial dysfunction, accelerated atherosclerosis, autonomic and peripheral neuropathy, structural penile changes, hormonal imbalances, and psychological factors. Methods A review of the literature was conducted to examine the pathophysiological mechanisms, genetic associations, and treatment modalities related to diabetic ED. Particular attention was given to studies exploring pharmacogenetics and emerging therapeutic interventions. Results Management is multimodal, including lifestyle changes, counselling, and pharmacological agents (primarily phosphodiesterase type 5 inhibitors (PDE5Is)), but treatment response varies. Genetic studies have identified associations between ED risk/severity and polymorphisms in several candidate genes, including NOS3 (G894T, T786C, VNTR), ARG1/ARG2 (influencing nitric oxide substrate availability), ACE (I/D polymorphism), AR (CAG repeat length affecting androgen sensitivity), and VEGF (promoter polymorphisms). Pharmacogenetic studies suggest that polymorphisms in NOS3, AR, and VEGF may predict response to PDE5Is or testosterone therapy, while ARG1/ARG2 variations might guide future arginase-targeted therapies. Emerging treatments like low-intensity shockwave therapy, platelet-rich plasma, gene therapy, and stem cell therapy show promise but require more robust evidence. Conclusions Diabetic ED is a complex condition driven by multiple pathophysiological mechanisms often influenced by an underlying genetic predisposition. Understanding the interplay between pathophysiology and genetics is crucial for developing personalised treatment strategies. While current therapies offer benefits, variability in response highlights the need for tailored approaches. Further research, especially large-scale pharmacogenetic studies and randomised controlled trials for emerging therapies, is essential to identify reliable biomarkers, optimise treatment selection, and improve outcomes for men with diabetic ED.

Language:English
Keywords:diabetes mellitus, erectile dysfunction, genetic polymorphisms, International Index of Erectile Function, pathophysiology
Work type:Article
Typology:1.02 - Review Article
Organization:MF - Faculty of Medicine
Publication status:Published
Publication version:Version of Record
Year:2025
Number of pages:23 str.
Numbering:Vol. 8, iss. 5, art. e70099
PID:20.500.12556/RUL-176653 This link opens in a new window
UDC:616.379
ISSN on article:2398-9238
DOI:10.1002/edm2.70099 This link opens in a new window
COBISS.SI-ID:249529091 This link opens in a new window
Publication date in RUL:11.12.2025
Views:393
Downloads:342
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Record is a part of a journal

Title:Endocrinology, diabetes & metabolism
Shortened title:Endocrinol. diabetes metab.
Publisher:Wiley & Sons
ISSN:2398-9238
COBISS.SI-ID:529715993 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:sladkorna bolezen, erektilna disfunkcija, genetski polimorfizmi

Projects

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0298
Name:Geni, hormonske in osebnostne spremembe pri metabolnih motnjah

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