JOURNAL ARTICLE
REVIEW
Genetics of erectile dysfunction.
Journal of Urology 2012 November
PURPOSE: Erectile dysfunction affects 50% of men older than 40 years. Recently more attempts have been made to identify genetic predictors of this disease. We reviewed animal and human data on genes related to the development and increased risk of erectile dysfunction.
MATERIALS AND METHODS: A literature search was performed using the PubMed® database. Articles addressing genes involved in erectile dysfunction were evaluated.
RESULTS: The majority of studies used a candidate gene approach to investigate genetic polymorphisms of known pathways mediating erection/detumescence. Studies in human and animal models are available. Human studies often compared the frequency of a specifically predetermined genetic polymorphism in men with erectile dysfunction to that in matched controls in whom few genes were persistently replicated. Several gene expression profiling studies are available that targeted specific erectile dysfunction models. Currently, there are few human genome wide association studies of erectile dysfunction.
CONCLUSIONS: Studies investigating the genetics of erectile dysfunction are mostly derived from animal models and candidate gene approaches. Candidate gene studies omit the greater portion of the genome, a problem that can be solved using a genome wide association study approach. The lack of persistently replicated results of candidate gene studies may be related to different patient ethnic backgrounds, variations in erectile dysfunction etiology and small sample sizes. Using strict inclusion/exclusion criteria for erectile dysfunction etiology and ethnicity in human studies may lead to improved understanding of the genetics of erectile dysfunction in specific populations.
MATERIALS AND METHODS: A literature search was performed using the PubMed® database. Articles addressing genes involved in erectile dysfunction were evaluated.
RESULTS: The majority of studies used a candidate gene approach to investigate genetic polymorphisms of known pathways mediating erection/detumescence. Studies in human and animal models are available. Human studies often compared the frequency of a specifically predetermined genetic polymorphism in men with erectile dysfunction to that in matched controls in whom few genes were persistently replicated. Several gene expression profiling studies are available that targeted specific erectile dysfunction models. Currently, there are few human genome wide association studies of erectile dysfunction.
CONCLUSIONS: Studies investigating the genetics of erectile dysfunction are mostly derived from animal models and candidate gene approaches. Candidate gene studies omit the greater portion of the genome, a problem that can be solved using a genome wide association study approach. The lack of persistently replicated results of candidate gene studies may be related to different patient ethnic backgrounds, variations in erectile dysfunction etiology and small sample sizes. Using strict inclusion/exclusion criteria for erectile dysfunction etiology and ethnicity in human studies may lead to improved understanding of the genetics of erectile dysfunction in specific populations.
Full text links
Trending Papers
Carvedilol, probably the β-blocker of choice for everyone with cirrhosis and portal hypertension: But not so fast!Liver International : Official Journal of the International Association for the Study of the Liver 2023 June
The five types of glomerulonephritis classified by pathogenesis, activity, and chronicity (GN-AC).Nephrology, Dialysis, Transplantation 2023 May 23
American Gastroenterological Association-American College of Gastroenterology Clinical Practice Guideline: Pharmacological Management of Chronic Idiopathic Constipation.Gastroenterology 2023 June
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app
Read by QxMD is copyright © 2021 QxMD Software Inc. All rights reserved. By using this service, you agree to our terms of use and privacy policy.
You can now claim free CME credits for this literature searchClaim now
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app