Vasectomy and prostate cancer risk: a pooled of cohort studies and Mendelian randomization analysis.

IF 3.4 2区 医学 Q2 ONCOLOGY BMC Cancer Pub Date : 2025-02-24 DOI:10.1186/s12885-025-13750-8
Li Wang, Si-Yu Chen, Shun Wan, Kun-Peng Li, Xiao-Ran Li, Li Yang
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Abstract

Background: The relationship between vasectomy and the risk of prostate cancer (PCa) remains unclear, with observational studies reporting inconsistent results. To clarify this ambiguity, we embarked on a comprehensive investigation comprising both a meta-analysis and a Mendelian randomization (MR) study. This dual approach aimed to thoroughly examine not only the association but also the causality between undergoing a vasectomy and the subsequent risk of PCa.

Methods: Our systematic review meticulously examined cohort studies published until January 2024, employing a random effects model for the computation of relative risks (RR) and their 95% confidence intervals (CI). For MR Analysis, we leveraged aggregated data from the IEU Open GWAS database, investigating the correlation between genetic predisposition to vasectomy and PCa. We chose single nucleotide polymorphisms (SNPs) of European descent as instrumental variables (IVs) for this analysis. The primary method for calculating the odds ratios (ORs) and their 95% CIs was inverse variance weighting (IVW). Through sensitivity analysis, we confirmed the robustness of our findings.

Results: Our investigation synthesized data from 19 cohort studies, encompassing over four million participants. The combined analysis revealed a statistically significant link between vasectomy and an elevated risk of PCa across any grade (RR = 1.09; 95%CI: 1.05-1.14; P = 0.001; I² = 83.3%). This association was observed for both localized PCa (RR = 1.08; 95% CI: 1.04-1.13; P < 0.001; I² = 48.8%) and advanced PCa (RR = 1.07; 95% CI: 1.01-1.13; P = 0.016; I² = 0%). Nonetheless, the discovery cohort MR Analysis indicated no genetic causal link between vasectomy and PCa (OR = 0.067; 95%CI = 0.002-1.535; P = 0.09). A validation set in the Finnish population confirmed the robustness of the results. This conclusion remained consistent even after controlling for variables such as prostate-specific antigen (PSA) testing and body mass index (BMI), suggesting that while a statistical association exists, the genetic evidence does not support a causal relationship.

Conclusion: The cumulative analysis indicates a possible elevated risk of PCa in patients who have had a vasectomy. However, MR Analysis has not confirmed a direct causal link between vasectomy and PCa. This suggests that the association observed may not stem from direct causation, allowing for the continued consideration of vasectomy as a viable long-term contraceptive choice. Further research is imperative to uncover any factors that could potentially link vasectomy to an increased risk of prostate cancer, aiming to provide a more comprehensive understanding of the implications.

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输精管切除术与前列腺癌风险:队列研究和孟德尔随机化分析的汇总。
背景:输精管切除术与前列腺癌(PCa)风险之间的关系尚不清楚,观察性研究报告的结果不一致。为了澄清这种模糊性,我们开展了一项综合调查,包括荟萃分析和孟德尔随机化(MR)研究。这种双重方法旨在彻底检查输精管切除术与前列腺癌后续风险之间的关系和因果关系。方法:我们的系统综述仔细检查了2024年1月之前发表的队列研究,采用随机效应模型计算相对风险(RR)及其95%置信区间(CI)。对于MR分析,我们利用来自IEU Open GWAS数据库的汇总数据,调查输精管切除术遗传易感性与PCa之间的相关性。我们选择欧洲血统的单核苷酸多态性(snp)作为分析的工具变量(IVs)。计算优势比(ORs)及其95% ci的主要方法是逆方差加权(IVW)。通过敏感性分析,我们证实了研究结果的稳健性。结果:我们的调查综合了19项队列研究的数据,涵盖了400多万参与者。综合分析显示,输精管切除术与任何级别的前列腺癌风险升高之间存在统计学意义上的联系(RR = 1.09;95%置信区间:1.05—-1.14;p = 0.001;I²= 83.3%)。两种局部PCa均存在这种关联(RR = 1.08;95% ci: 1.04-1.13;结论:累积分析表明,输精管切除术患者患前列腺癌的风险可能升高。然而,磁共振分析并没有证实输精管切除术和前列腺癌之间的直接因果关系。这表明所观察到的关联可能不是源于直接的因果关系,允许继续考虑输精管切除术作为一种可行的长期避孕选择。进一步的研究是必要的,以揭示任何可能将输精管切除术与前列腺癌风险增加联系起来的因素,旨在提供对其影响的更全面的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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