Luo Yurui, Su Shiqi, Yang Yong, Xiang Nanyan, Fu Tingting, Lui Su, Lin Yifei, Huang Jin
Department of Urology, Innovation Institute for Integration of Medicine and Engineering, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, China.
Innovation Institute for Integration of Medicine and Engineering, West China Hospital, Sichuan University, Chengdu, China.
Transl Androl Urol. 2024 Nov 30;13(11):2439-2447. doi: 10.21037/tau-24-321. Epub 2024 Nov 28.
Recently, some observational studies have suggested potential associations between erectile dysfunction (ED) and respiratory function. However, the underlying biological mechanisms and causal relationships between ED and lung function require further investigation. This study aimed to explore the causalities between ED and lung function traits.
Single-nucleotide polymorphisms (SNPs) for ED were extracted from the Finngen_r7 (1,154 cases and 94,024 controls), and the summary statistics of respiratory function were extracted from the UK Biobank (UKB) (n=321,047). We utilized several Mendelian randomization (MR) methods to mitigate the impact of weak instrument bias and pleiotropy. To address potential confounding effects, multivariable MR (MVMR) analyses were also conducted, adjusting for demographic factors and respiratory conditions. Moreover, recently developed latent causal variable (LCV) modeling was also performed to enhance the robustness of the findings.
Totally 15 SNPs robustly associated with ED were included. We found that higher risk of ED was associated with decreased of forced expiratory volume in the first second (FEV1) [odds ratio (OR) 0.992, 95% confidence interval (CI): 0.986, 0.997, P=0.003], as was the case for forced vital capacity (FVC) (OR 0.994, 95% CI: 0.989, 1.000, P=0.04), peak expiratory flow (PEF) (OR 0.990, 95% CI: 0.990, 0.990, P=0.01) and FEV1/FVC ratio (OR 0.991, 95% CI: 0.985, 0.997, P=0.002). After adjusting for confounding factors, ED only demonstrated causal effects on FEV1/FVC ratio. Notably, the LCV analysis provided additional support for the positive causal impact of ED on FEV1 and FVC. Conversely, reverse MR analysis did not reveal compelling evidence for a causal effect of lung function on ED.
Our study suggests a potential causal relationship between higher ED susceptibility and reduced respiratory function, as indicated by decreased FEV1, FVC, PEF, and the FEV1/FVC ratio. The results enhanced understanding of the intricate interrelationships between ED and lung function.
最近,一些观察性研究表明勃起功能障碍(ED)与呼吸功能之间可能存在关联。然而,ED与肺功能之间潜在的生物学机制和因果关系仍需进一步研究。本研究旨在探讨ED与肺功能特征之间的因果关系。
从芬兰基因库r7(1154例病例和94024例对照)中提取ED的单核苷酸多态性(SNP),并从英国生物银行(UKB)(n = 321047)中提取呼吸功能的汇总统计数据。我们采用了几种孟德尔随机化(MR)方法来减轻弱工具偏倚和多效性的影响。为了解决潜在的混杂效应,还进行了多变量MR(MVMR)分析,对人口统计学因素和呼吸状况进行了调整。此外,还进行了最近开发的潜在因果变量(LCV)建模,以增强研究结果的稳健性。
共纳入15个与ED密切相关的SNP。我们发现,ED风险较高与第一秒用力呼气量(FEV1)降低相关[优势比(OR)0.992,95%置信区间(CI):0.986,0.997,P = 0.003],用力肺活量(FVC)(OR 0.994,95% CI:0.989,1.000,P = 0.04)、呼气峰值流速(PEF)(OR 0.990,95% CI:0.990,0.990,P = 0.01)和FEV1/FVC比值(OR 0.991,95% CI:0.985,0.997,P = 0.002)情况相同。在调整混杂因素后,ED仅对FEV1/FVC比值显示出因果效应。值得注意的是,LCV分析为ED对FEV1和FVC的正向因果影响提供了额外支持。相反,反向MR分析未发现肺功能对ED有因果效应的令人信服的证据。
我们的研究表明,较高的ED易感性与呼吸功能降低之间可能存在因果关系,表现为FEV1、FVC、PEF和FEV1/FVC比值降低。这些结果加深了对ED与肺功能之间复杂相互关系的理解。