Erectile Dysfunction Predicts Cardiovascular Events as an Independent Risk Factor: A Systematic Review and Meta-Analysis

被引:72
|
作者
Zhao, Binghao [1 ,2 ,3 ]
Hong, Zhengdong [4 ]
Wei, Yiping [4 ]
Yu, Dongliang [1 ]
Xu, Jianjun [1 ]
Zhang, Wenxiong [1 ]
机构
[1] Nanchang Univ, Affiliated Hosp 2, Dept Thorac Surg, Nanchang, Jiangxi, Peoples R China
[2] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Neurosurg, Beijing, Peoples R China
[3] Peking Union Med Coll, Beijing, Peoples R China
[4] Nanchang Univ, Affiliated Hosp 2, Dept Urol, Nanchang, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Erectile Dysfunction; Cardiovascular Disease; Coronary Heart Disease; Stroke; Meta-Analysis; CORONARY-ARTERY-DISEASE; HEART-DISEASE; ATRIAL-FIBRILLATION; METABOLIC SYNDROME; MEN; POPULATION; MORTALITY; PREVALENCE; STROKE; COHORT;
D O I
10.1016/j.jsxm.2019.04.004
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Previous studies demonstrating that erectile dysfunction (ED) predicts the risk of further cardiovascular events (CV) events are insufficient to make recommendations for cardiologists, diabetologists, urologists, and more, and the association between CV events and ED degree is unclear. Aim: To assess whether ED was a risk factor for CV events in a comprehensive literature review and meta-analysis. Methods: PubMed, EMBASE, the Cochrane Library, Medline, and the Web of Science were searched for eligible studies. The protocol for this meta-analysis is available from PROSPERO (CRD42018086138). Main Outcome Measures: The main outcomes included cardiovascular disease (CVD), coronary heart disease (CHD), stroke, and all-cause mortality. Subgroup and sensitivity analyses were conducted to detect potential bias. Results: 25 eligible studies involving 154,794 individuals were included in our meta-analysis. Compared with those of men without ED, the CVD risk of ED patients was significantly increased by 43% (relative risk [RR] = 1.43; P < .001), CHD was increased by 59%(RR = 1.59; P < .001), stroke was increased by 34%(RR = 1.34; P < .001), and all-cause mortality was increased by 33%(RR = 1.33; P < .001). Older individuals with ED (>= 55 years), those with ED of a shorter duration (<7 years), and those with higher rates of diabetes (>= 20%) and smoking (>= 40%) were more prone to develop CVD. Additionally, severe ED was proven to predict higher CVD and all-cause mortality risk. The standardized model proposed here can be properly applied for screening early CV events. Clinical Implications: The evidence prompts the diligent observation of at-risk men and reinforces the importance of early treatment to prevent CV events. Strengths & Limitations: Larger sample sizes from recent prospective cohort studies were included to provide more up-to-date, reliable, and comprehensive results. Moreover, the results were robust regarding consistency across sensitivity and subgroup analyses and remained consistent; even pre-excluded retrospective or cross-sectional studies were included. We constructed a standardized model that addresses the study's innovations and implications for the first time. However, not all included studies were randomized controlled trials, which might downgrade this evidence. Conclusions: Risk of total CVD, CHD, stroke, and all-cause mortality was significantly increased in populations with ED, and severe ED is of particular concern. The evidence suggests the need for diligent observation of at-risk men and reinforces the importance of early treatment to prevent CV events. Copyright (C) 2019, International Society for Sexual Medicine. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1005 / 1017
页数:13
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