Insights into modifiable risk factors of erectile dysfunction, a wide-angled Mendelian Randomization study

被引:35
|
作者
Xiong, Yang [1 ,2 ]
Zhang, Fuxun [1 ,2 ]
Zhang, Yangchang [3 ]
Wang, Wei [1 ,2 ]
Ran, Yuxin [4 ]
Wu, Changjing [2 ]
Zhu, Shiyu [1 ,2 ]
Qin, Feng [2 ]
Yuan, Jiuhong [1 ,2 ,5 ]
机构
[1] Sichuan Univ, West China Hosp, Androl Lab, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Urol, Chengdu 610041, Peoples R China
[3] Capital Med Univ, Dept Publ Hlth, Beijing 100000, Peoples R China
[4] Chongqing Med Univ, Women & Childrens Hosp, Ctr Reprod Med, Chongqing, Peoples R China
[5] Sichuan Univ, West China Hosp, Dept Urol, Androl Lab, 37 Guoxue Alley, Chengdu 610041, Sichuan, Peoples R China
关键词
Cardiovascular diseases; Erectile dysfunction; Lifestyle factors; Mendelian randomization; Metabolic diseases; Mental disorder; SEXUAL DYSFUNCTION; ABDOMINAL OBESITY; MEN; PREVALENCE; ASSOCIATION; SYMPTOMS; DISORDER; DISEASE; HEALTH; LEVEL;
D O I
10.1016/j.jare.2023.05.008
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: The causal association between modifiable risk factors and erectile dysfunction (ED) remains unclear, which hinders the early identification and intervention of patients with ED. The present study aimed to clarify the causal association between 42 predominant risk factors and ED. Methods: Univariate Mendelian Randomization (MR), multivariate MR, and mediation MR analyses were used to investigate the causal association between 42 modifiable risk factors and ED. Combined results were pooled from two independent ED genome-wide association studies to verify the findings. Results: Genetically predicted body mass index (BMI), waist circumference, trunk fat mass, whole body fat mass, poor overall health rating, type 2 diabetes, basal metabolic rate, adiponectin, cigarette consumption, insomnia, snoring, hypertension, stroke, ischemic stroke, coronary heart disease, myocardial infarction, heart failure, and major depressive disorder were found to increase the risk of ED (all P < 0.05). Additionally, genetic liability to higher body fat percentage and alcohol consumption were suggestively associated with an increased risk of ED (P < 0.05 and adjusted P > 0.05). Genetic predisposition to higher sex hormone-binding globulin (SHBG) levels could decrease the risk of ED (P < 0.05). No significant association was detected between lipid levels and ED. Multivariate MR identified type 2 diabetes, basal metabolic rate, cigarette consumption, hypertension, and coronary heart disease as risk factors for ED. The combined results confirmed that waist circumference, whole body fat mass, poor overall health rating, type 2 diabetes, basal metabolic rate, adiponectin, cigarette consumption, snoring, hypertension, ischemic stroke, coronary heart disease, myocardial infarction, heart failure, and major depressive disorder could increase the risk of ED (all P < 0.05), while higher SHBG decreased the risk of ED (P = 0.004). There were suggestive significances of BMI, insomnia, and stroke on ED (P < 0.05 and adjusted P > 0.05). Conclusion: This comprehensive MR study supported the causal role of obesity, type 2 diabetes, basal metabolic rate, poor self-health rating, cigarette and alcohol consumption, insomnia and snoring, depression, hypertension, stroke, ischemic stroke, coronary heart disease, myocardial infarction, heart failure, SHBG, and adiponectin in the onset and development of ED. (c) 2024 The Authors. Published by Elsevier B.V. on behalf of Cairo University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:149 / 161
页数:13
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