抑郁症对前列腺炎的因果影响:免疫细胞介导的两步孟德尔随机研究。

IF 1.7
Feifan Liu, Lijun Han, Jianyu Wang, Yufeng Song, Fei Wu, Haihu Wu, Jiaju Lyu, Hao Ning
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引用次数: 0

摘要

背景:抑郁症对全球有重大影响。以往的研究表明,抑郁症与前列腺疾病之间存在联系。然而,这些研究通常是观察性的,可能会受到混杂因素和反向因果关系的影响。本研究旨在利用孟德尔随机法(MR)探讨抑郁症与前列腺疾病之间的潜在因果关系,并评估免疫细胞表型的中介作用:我们利用全基因组关联研究(GWAS)数据采用了孟德尔随机化方法。分析分两个阶段进行:(a) 双样本 MR,研究抑郁症对前列腺疾病的影响;(b) 两步 MR,评估 731 种免疫细胞表型的中介作用。抑郁症数据来自一项广泛的全球基因组研究,涉及多个欧洲队列的 480 359 名参与者。前列腺疾病数据(包括前列腺炎、前列腺癌和良性前列腺增生)来自欧洲的 GWAS。与抑郁症相关的独立单核苷酸多态性是根据全基因组显著性标准筛选出来的。采用了各种 MR 方法,包括反方差加权、加权中位数、MR-Egger、MR-PRESSO、MR-Robust 和 MR-RAPS,以确保稳健的因果推断:MR分析显示抑郁与前列腺炎风险增加之间存在潜在的因果关系(几率比=1.606,P=8.35E-04)。敏感性分析证实了这些结果的稳健性。此外,两步MR分析发现CD24+ CD27+ %淋巴细胞是潜在的中介因子,其中介效应为0.108(P = 0.03),占总效应的22.78%:本研究为抑郁症与前列腺炎之间的因果关系提供了新的遗传学证据,免疫细胞被确定为这一过程中的潜在调解因子。这些发现凸显了心理因素在前列腺炎发病中的重要性,并表明免疫细胞可能成为新的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Causal effects of depression on prostatitis: a two-step Mendelian randomisation study with immune cell mediation.

Background: Depression has a significant global impact. Previous studies have suggested a link between depression and prostate diseases. However, these studies are often observational and may be influenced by confounding factors and reverse causality. This research aimed to explore the potential causal relationship between depression and prostate diseases using Mendelian randomisation (MR) and to assess the mediating role of immune cell phenotypes.

Methods: We utilised MR methods with genome-wide association studies (GWAS) data. The analysis was conducted in two phases: (a) a two-sample MR to investigate the impact of depression on prostate diseases; and (b) a two-step MR to evaluate the mediating effect of 731 immune cell phenotypes. Depression data were obtained from an extensive GWAS involving 480 359 participants across multiple European cohorts. Prostate disease data, including prostatitis, prostate cancer, and benign prostatic hyperplasia, were obtained from European-based GWAS. Independent single nucleotide polymorphisms related to depression were selected based on genome-wide significance criteria. Various MR methods, including inverse variance weighting, weighted median, MR-Egger, MR-PRESSO, MR-Robust, and MR-RAPS, were employed to ensure robust causal inference.

Results: The MR analysis revealed a potential causal relationship between depression and an increased risk of prostatitis (odds ratio = 1.606, P = 8.35E-04). Sensitivity analysis confirmed the robustness of these findings. Additionally, a two-step MR analysis identified CD24+ CD27+ %lymphocytes as a potential mediator, with a mediation effect of 0.108 (P = 0.03), accounting for 22.78% of the total effect.

Conclusions: This study offers novel genetic evidence for the causal relationship between depression and prostatitis, with immune cells identified as potential mediators in this process. These findings highlight the importance of psychological factors in developing prostatitis and suggest that immune cells could be novel therapeutic targets.

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