Drs. Guo and Liao contributed equally to the manuscript.
Erectile Dysfunction and Risk of Clinical Cardiovascular Events: A Meta-Analysis of Seven Cohort Studies
Article first published online: 30 MAR 2010
© 2010 International Society for Sexual Medicine
The Journal of Sexual Medicine
Volume 7, Issue 8, pages 2805–2816, August 2010
How to Cite
Guo, W., Liao, C., Zou, Y., Li, F., Li, T., Zhou, Q., Cao, Y. and Mao, X. (2010), Erectile Dysfunction and Risk of Clinical Cardiovascular Events: A Meta-Analysis of Seven Cohort Studies. Journal of Sexual Medicine, 7: 2805–2816. doi: 10.1111/j.1743-6109.2010.01792.x
- Issue published online: 2 AUG 2010
- Article first published online: 30 MAR 2010
- Erectile Dysfunction;
- Endothelial Dysfunction;
- Cardiovascular Disease Events;
- All-Cause Mortality;
- Myocardial Infarction;
Introduction. For many years, erectile dysfunction (ED) has been considered as a complication of cardiovascular disease (CVD) or regarded as a late consequence of generalized arterial disease. However, a growing body of evidence suggests that ED is an early manifestation of atherosclerosis and a precursor to systemic vascular disease.
Aim. We conducted a meta-analysis to evaluate the association between ED and the risk of CVD events.
Methods. Relevant studies published between January 1966 and September 2009 were identified by searching Medline, Embase, and The Cochrane Library. Studies were selected using a prior defined criteria. The strength of the relationship between ED and CVD events was assessed by adjusted relative risks (RRs).
Main Outcome Measures. The adjusted RRs of CVD events.
Results. A total of 45,558 participants from seven cohort studies (eight full-text articles) were identified in this meta-analysis. The studies provided adjusted RRs estimates for ED subjects comparing with health subjects, leading to a pooled adjusted RR of 1.47 (95% confidence interval [CI], 1.29–1.66, P < 0.001; P for heterogeneity = 0.152; I2 = 36.2%) for CVD events. The risks of CVD, all-cause mortality and myocardial infarction were 1.41 (95% CI, 1.22–1.64 P < 0.001), 1.23 (95% CI, 1.02–1.48; P = 0.034), and 1.43 (95% CI, 1.10–1.85 P = 0.007), respectively. The overall adjusted RR decreased significant from 1.63 (<7 years) to 1.37 (≥7 years) along with the elongation of follow-up.
Conclusions. There is evidence of an increased risk of CVD events for patients with ED. Patients who are discovered to have ED are supposed to be thoroughly assessed for cardiovascular risk and occult systemic vascular disease. Guo W, Liao C, Zou Y, Li F, Li T, Zhou Q, Cao Y, and Mao X. Erectile dysfunction and risk of clinical cardiovascular events: A meta-analysis of seven cohort studies. J Sex Med 2010;7:2805–2816.