{"title":"Understanding the erectile dysfunction-cardiovascular disease connection: clinical and pathophysiological insights.","authors":"Jinshun An, Boyu Xiang, Jingxuan Peng, Dongjie Li","doi":"10.1093/sxmrev/qeaf014","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Erectile dysfunction (ED) and cardiovascular disease (CVD) share common pathophysiological mechanisms and molecular pathways, with ED serving as an independent risk factor and prognostic marker for CVD.</p><p><strong>Objectives: </strong>This review aims to explore the relationship between ED and CVD, analyze their shared pathophysiological mechanisms, and discuss the implications of these findings for clinical practice.</p><p><strong>Methods: </strong>A comprehensive literature review was conducted using PubMed, MEDLINE, and Web of Science databases, with keywords including \"erectile dysfunction,\" \"cardiovascular disease,\" \"endothelial dysfunction,\" \"inflammation,\" \"oxidative stress,\" \"NO/cGMP/PKG signaling pathway,\" \"RhoA/ROCK pathway,\" and \"testosterone deficiency.\"</p><p><strong>Results: </strong>The study found a positive correlation between ED and the incidence rate and severity of CVD, with shared mechanisms such as endothelial dysfunction, oxidative stress, and systemic inflammation. Mendelian randomization studies provided evidence of a causal relationship between genetically predicted CVD and ED risk, although reverse causality remains less clear. Early detection of ED may help prevent and manage CVD, with ED serving as a sentinel marker for asymptomatic coronary artery disease. The review also highlighted the potential of combining treatments like phosphodiesterase type 5 inhibitors with rho-associated protein kinase inhibitors or glucagon-like peptide-1 receptor agonists with testosterone therapy to optimize both cardiovascular and sexual outcomes.</p><p><strong>Conclusions: </strong>Understanding the association between ED and CVD is crucial for improving patients' quality of life and cardiovascular prognosis. Future research should focus on elucidating the mechanistic pathways underlying ED and CVD, validating causal relationships through long-term, multimodal studies, and developing standardized risk algorithms for early intervention. For clinical practice, proactive ED screening in high-risk populations and interdisciplinary collaboration between cardiologists and urologists are essential to prevent CVD progression and enhance patient quality of life.</p>","PeriodicalId":21813,"journal":{"name":"Sexual medicine reviews","volume":" ","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sexual medicine reviews","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/sxmrev/qeaf014","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
导言:勃起功能障碍(ED)和心血管疾病(CVD)有着共同的病理生理机制和分子途径,ED是心血管疾病的独立危险因素和预后标志:本综述旨在探讨 ED 与心血管疾病之间的关系,分析它们共同的病理生理机制,并讨论这些发现对临床实践的影响:方法:使用PubMed、MEDLINE和Web of Science数据库进行了全面的文献综述,关键词包括 "勃起功能障碍"、"心血管疾病"、"内皮功能障碍"、"炎症"、"氧化应激"、"NO/cGMP/PKG信号通路"、"RhoA/ROCK通路 "和 "睾酮缺乏":研究发现,ED与心血管疾病的发病率和严重程度呈正相关,其共同机制包括内皮功能障碍、氧化应激和全身炎症。孟德尔随机化研究提供了基因预测心血管疾病与 ED 风险之间存在因果关系的证据,但反向因果关系仍不太明确。早期发现 ED 可能有助于预防和控制心血管疾病,ED 可作为无症状冠状动脉疾病的哨点标志物。综述还强调了将5型磷酸二酯酶抑制剂与rho相关蛋白激酶抑制剂或胰高血糖素样肽-1受体激动剂与睾酮治疗相结合,以优化心血管和性功能结果的潜力:了解 ED 与心血管疾病之间的关联对于改善患者的生活质量和心血管疾病的预后至关重要。未来的研究应侧重于阐明 ED 和心血管疾病的机理途径,通过长期、多模式研究验证因果关系,并为早期干预制定标准化的风险算法。在临床实践中,对高危人群进行积极的 ED 筛查以及心脏病专家和泌尿科专家之间的跨学科合作对于预防心血管疾病的恶化和提高患者的生活质量至关重要。
Understanding the erectile dysfunction-cardiovascular disease connection: clinical and pathophysiological insights.
Introduction: Erectile dysfunction (ED) and cardiovascular disease (CVD) share common pathophysiological mechanisms and molecular pathways, with ED serving as an independent risk factor and prognostic marker for CVD.
Objectives: This review aims to explore the relationship between ED and CVD, analyze their shared pathophysiological mechanisms, and discuss the implications of these findings for clinical practice.
Methods: A comprehensive literature review was conducted using PubMed, MEDLINE, and Web of Science databases, with keywords including "erectile dysfunction," "cardiovascular disease," "endothelial dysfunction," "inflammation," "oxidative stress," "NO/cGMP/PKG signaling pathway," "RhoA/ROCK pathway," and "testosterone deficiency."
Results: The study found a positive correlation between ED and the incidence rate and severity of CVD, with shared mechanisms such as endothelial dysfunction, oxidative stress, and systemic inflammation. Mendelian randomization studies provided evidence of a causal relationship between genetically predicted CVD and ED risk, although reverse causality remains less clear. Early detection of ED may help prevent and manage CVD, with ED serving as a sentinel marker for asymptomatic coronary artery disease. The review also highlighted the potential of combining treatments like phosphodiesterase type 5 inhibitors with rho-associated protein kinase inhibitors or glucagon-like peptide-1 receptor agonists with testosterone therapy to optimize both cardiovascular and sexual outcomes.
Conclusions: Understanding the association between ED and CVD is crucial for improving patients' quality of life and cardiovascular prognosis. Future research should focus on elucidating the mechanistic pathways underlying ED and CVD, validating causal relationships through long-term, multimodal studies, and developing standardized risk algorithms for early intervention. For clinical practice, proactive ED screening in high-risk populations and interdisciplinary collaboration between cardiologists and urologists are essential to prevent CVD progression and enhance patient quality of life.