Li Hong, Wen Zheng
Department of Medical Administration, Minzu Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
Department of Epidemiology, School of Public Health, Guangxi Medical University, Nanning, China.
Front Genet. 2022 Aug 15;13:846005. doi: 10.3389/fgene.2022.846005. eCollection 2022.
Both ulcerative colitis (UC) and Crohn's disease (CD) are associated with neurodegenerative diseases (NDs) in observational studies, but the causality remains controversial. We aimed to use Mendelian randomization (MR) analysis to explore causal associations between UC and CD and NDs. We used single nucleotide polymorphisms (SNPs) associated ( < 5 × 10) with UC and CD as instrumental variables (IVs) to perform the MR analysis on the risks of three NDs, namely, Alzheimer's Disease (AD), Parkinson's Disease (PD), and Amyotrophic Lateral Sclerosis (ALS). The inverse variance weighted (IVW) was the primary method and supplement with the weighted median and MR-Egger regression. Moreover, the MR-Egger intercept test, Cochran's Q test, and "leave one out" sensitivity analysis were implemented to assess the horizontal pleiotropy, heterogeneities, and stability of these SNPs on NDs. To verify the stability of the results, we re-run the MR analysis by using another set of IVs of UC and CD. A reverse causality analysis was conducted to test whether NDs were causally associated with UC or CD. The significance threshold was set at < 0.05/6 = 0.008. In the primary MR analysis, the IVW method yielded no evidence to support a causal association between UC and PD (: 1.01, 95% : 0.96-1.06, = 0.65), AD (: 1.00, 95% : 0.99-1.00, = 0.57), or ALS (: 0.98, 95% : 0.96-1.01, = 0.24), and neither did the MR-Egger and weighted median methods. Our MR analysis also suggested no definitively causal effect of the genetically predicted CD on PD (: 1.01, 95% : 0.97-1.05, = 0.54), AD (: 1.00, 95% : 0.99-1.00, = 0.26), or ALS (: 0.99, 95% : 0.96-1.02, = 0.41), as well as MR-Egger and weighted median methods. Consistent results were found in validation analyses. We did not find a significant causal effect of NDs on UC or CD in the reverse MR analysis. No evidence indicated an association between the risks of NDs and genetically predicted UC or CD. The MR results did not support a causal association between UC or CD and three NDs.
在观察性研究中,溃疡性结肠炎(UC)和克罗恩病(CD)均与神经退行性疾病(NDs)相关,但因果关系仍存在争议。我们旨在使用孟德尔随机化(MR)分析来探究UC、CD与NDs之间的因果关联。我们使用与UC和CD相关的单核苷酸多态性(SNP,<5×10)作为工具变量(IV),对三种NDs(即阿尔茨海默病(AD)、帕金森病(PD)和肌萎缩侧索硬化症(ALS))的风险进行MR分析。逆方差加权(IVW)是主要方法,并辅以加权中位数和MR-Egger回归。此外,实施MR-Egger截距检验、 Cochr an Q检验和“留一法”敏感性分析,以评估这些SNP对NDs的水平多效性、异质性和稳定性。为验证结果的稳定性,我们使用另一组UC和CD的IV重新进行MR分析。进行反向因果分析以检验NDs是否与UC或CD存在因果关联。显著性阈值设定为<0.05/6 = 0.008。在主要的MR分析中,IVW方法未提供证据支持UC与PD(比值比:1.01,95%置信区间:[0.96,1.06],P = 0.65)、AD(比值比:1.00,95%置信区间:[0.99,1.00],P = 0.57)或ALS(比值比:0.98,95%置信区间:[0.96,1.01],P = 0.24)之间存在因果关联,MR-Egger和加权中位数方法也未提供支持。我们的MR分析还表明,基因预测的CD对PD(比值比:1.01,95%置信区间:[0.97,1.05],P = 0.54)、AD(比值比:1.00,95%置信区间:[0.99,1.00],P = 0.26)或ALS(比值比:0.99,95%置信区间:[0.96,1.02],P = 0.41)也没有明确因果效应,MR-Egger和加权中位数方法同样如此。在验证分析中得到了一致的结果。在反向MR分析中,我们未发现NDs对UC或CD有显著因果效应。没有证据表明NDs风险与基因预测的UC或CD之间存在关联。MR结果不支持UC或CD与三种NDs之间存在因果关联。