Causal relationship between educational attainment and Hashimoto's thyroiditis: a two-sample mendelian randomization study.

Rongjia Zhang, Yulu Chen, Xian Deng, Xu Li, Dehui Qiao, Hui Yang
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Abstract

Introduction: The etiology of Hashimoto's thyroiditis (HT) is diverse. The correlation between educational attainment (EA) and health is also a research hotspot. This study explores the relationship between EA and HT from a genetic perspective.

Material and methods: Summary data on EA and HT were sourced from the MRC Integrative Epidemiology Unit (IEU) Open Genome-Wide Association Studies (GWAS) database. Utilizing single nucleotide polymorphisms (SNPs) that are strongly associated with EA as instrumental variables, we estimated the causal relationship between EA and HT through two-sample mendelian randomization (TSMR) analysis, including inverse variance weighted (IVW), MR-Egger, weighted median, simple mode, and weighted mode approaches. Heterogeneity was assessed using Cochran's Q test. Pleiotropy was evaluated via the MR-Egger intercept and the global test value from MR pleiotropy residual sum and outlier (MR-PRESSO). Additionally, a leave-one-out method along with funnel plot analysis was employed to examine stability.

Results: The IVW method revealed a significant correlation between EA and HT [odds ratio (OR): 0.933, 95% confidence interval (CI): 0.898 to 0.970, p < 0.001], while similar evidence was observed using the weighted median method (OR: 0.938, 95% CI: 0.886 to 0.993, p = 0.029). Cochran's Q test indicated no heterogeneity (p > 0.05). Both the intercept value and global test result suggested an absence of pleiotropy (p > 0.05). The leave-one-out approach did not identify any individual SNP exerting a significant influence on the overall effect estimate. Furthermore, scatter points in the funnel plot exhibited near symmetry, indicating robust study stability.

Conclusion: EA is associated with lower risk of HT.

教育程度与桥本甲状腺炎的因果关系:一项双样本孟德尔随机化研究。
桥本甲状腺炎(HT)的病因多样。受教育程度与健康的关系也是一个研究热点。本研究从遗传学角度探讨EA与HT之间的关系。材料和方法:EA和HT的汇总数据来自MRC综合流行病学单位(IEU)开放全基因组关联研究(GWAS)数据库。利用与EA密切相关的单核苷酸多态性(snp)作为工具变量,我们通过双样本孟德尔随机化(TSMR)分析,包括方差反加权(IVW)、MR-Egger、加权中位数、简单模式和加权模式方法,估计了EA和HT之间的因果关系。异质性采用Cochran’s Q检验。通过MR- egger截距和MR多效性残差和离群值(MR- presso)的全局检验值来评估多效性。此外,采用留一法和漏斗图分析来检验稳定性。结果:IVW法显示EA与HT之间存在显著相关性[比值比(OR): 0.933, 95%可信区间(CI): 0.898 ~ 0.970, p < 0.001],加权中位数法观察到类似的证据(OR: 0.938, 95% CI: 0.886 ~ 0.993, p = 0.029)。Cochran’s Q检验无异质性(p < 0.05)。截距值和整体检验结果均提示不存在多效性(p < 0.05)。“留一”方法没有发现任何对总体效果估计产生重大影响的单个SNP。此外,漏斗图中的散点表现出接近对称性,表明研究稳定性强。结论:EA与较低的HT发病风险相关。
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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