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Published on: December 28, 2021
Cardiovascular risk among men seeking help for erectile dysfunction
J Frantzen1, T G W Speel, L A Kiemeney
1Radboud University Medical Centre, Nijmegen, the Netherlands. j.frantzen@vumc.nl
Insights
Erectile dysfunction (ED) was a marker for cardiovascular disease (CVD) before sildenafil, but not after its introduction. The study investigated the link between ED and CVD risk in men.
Area of Science:
- Cardiovascular Medicine
- Urology
- Epidemiology
Background:
- Erectile dysfunction (ED) prevalence and its association with cardiovascular disease (CVD) became a significant clinical concern following sildenafil's introduction.
- Physicians questioned whether ED serves as an early indicator for underlying CVD.
Purpose of the Study:
- To investigate the relationship between ED and the risk of developing CVD.
- To determine if ED remains a sentinel marker for CVD after the widespread availability of sildenafil.
Main Methods:
- A historical cohort study utilized general practice medical records from the Netherlands.
- Incident ED cases and controls (men without ED) were identified from a population of 60,000 men aged 35-74 years.
- CVD incidence was compared between men with and without ED before and after sildenafil's introduction.
Main Results:
- The incidence of ED doubled post-sildenafil introduction (5.3 to 10.1 per 1000 men-years).
- The relative risk of CVD in men with ED was 1.7 before sildenafil (95% CI 0.9-3.3) and 1.1 afterwards (95% CI 0.6-1.8).
Conclusions:
- ED was a significant marker for CVD risk prior to sildenafil's market entry.
- The association between ED and CVD risk diminished significantly after sildenafil became available, suggesting ED is no longer a reliable CVD sentinel in this context.
Purpose:
The introduction of sildenafil put the risk of cardiovascular disease (CVD) among men with erectile dysfunction (ED) on the agenda of physicians. The question arose, Is EDsentinel to CVD? We sought to answer this question in the present study.
Methods:
A historical cohort study was set up using medical records of general practices all over the Netherlands. Incident cases of ED were selected before and after the introduction of sildenafil using a catchment population of 60,000 men aged 35 to 74 years. Two to three men without ED (controls) were, subsequently, matched to each case. Incidence of CVD was determined for cases and controls, respectively.
Results:
Overall, incidence of ED doubled from 5.3 per 1000 men-years in the period before introduction of sildenafil to 10.1 after the introduction. The relative risk of incident CVD among men with ED compared to controls was 1.7 [95%-CI 0.9-3.3] before the introduction and 1.1 [95%-CI 0.6-1.8] afterwards.
Conclusions:
While ED could be seen as a marker for CVD before the introduction of sildenafil, it was clearly not afterwards.
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