吸烟与慢性肾脏病 3 至 5 期的关系:孟德尔随机研究。

Health data science Pub Date : 2024-11-04 eCollection Date: 2024-01-01 DOI:10.34133/hds.0199
Zhilong Zhang, Feifei Zhang, Xiaomeng Zhang, Lanlan Lu, Luxia Zhang
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引用次数: 0

摘要

背景:以前的研究表明,吸烟行为(如吸烟状态)与慢性肾脏病(CKD)风险升高有关,但这种关联是否是因果关系仍不确定。研究方法我们使用了英国生物库队列中 50 万名 40 至 69 岁参与者的数据。在传统的观察性研究中,我们使用 Cox 比例危险模型来计算两个吸烟指数--吸烟状态和终生吸烟指数--与 CKD 3 至 5 期事件之间的关系。孟德尔随机化(MR)方法用于估计潜在的因果效应。在单样本 MR 中,我们将与终生吸烟指数相关的基因变异作为工具变量,在 344,255 名英国生物库参与者(英国白人血统)中检验与 CKD 3 至 5 期的因果关系。我们利用慢性肾脏病遗传学联盟全基因组关联研究的信息,通过双样本 MR 分析进一步验证了我们的研究结果。研究结果在传统的观察性研究中,吸烟状况[危险比(HR):1.26,95% 置信区间(CI):1.22 至 1.30]和终生吸烟指数(HR:1.22,95% CI:1.20 至 1.24)均与较高的慢性肾脏病发病风险呈正相关。然而,我们的单样本和双样本 MR 分析表明,终生吸烟指数与 CKD 之间没有因果关系(所有 P > 0.05)。遗传工具已通过多项统计检验得到验证,所有敏感性分析均显示出与主模型相似的结果。结论我们分析的证据并不表明吸烟行为对 CKD 风险有因果效应。传统观察研究中出现的正相关可能是混杂因素造成的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Smoking with Chronic Kidney Disease Stages 3 to 5: A Mendelian Randomization Study.

Background: Previous studies suggested that smoking behavior (e.g., smoking status) was associated with an elevated risk of chronic kidney disease (CKD), yet whether this association is causal remains uncertain. Methods: We used data for half million participants aged 40 to 69 years from the UK Biobank cohort. In the traditional observational study, we used Cox proportional hazards models to calculate the associations between 2 smoking indices-smoking status and lifetime smoking index and incident CKD stages 3 to 5. Mendelian randomization (MR) approaches were used to estimate a potential causal effect. In one-sample MR, genetic variants associated with lifetime smoking index were used as instrument variables to examine the causal associations with CKD stages 3 to 5, among 344,255 UK Biobank participants with white British ancestry. We further validated our findings by a two-sample MR analysis using information from the Chronic Kidney Disease Genetics Consortium genome-wide association study. Results: In the traditional observational study, both smoking status [hazard ratio (HR): 1.26, 95% confidence interval (CI): 1.22 to 1.30] and lifetime smoking index (HR: 1.22, 95% CI: 1.20 to 1.24) were positively associated with a higher risk of incident CKD. However, both our one-sample and two-sample MR analyses showed no causal association between lifetime smoking index and CKD (all P > 0.05). The genetic instruments were validated by several statistical tests, and all sensitivity analyses showed similar results with the main model. Conclusion: Evidence from our analyses does not suggest a causal effect of smoking behavior on CKD risk. The positive association presented in the traditional observational study is possibly a result of confounding.

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