Han Zesen, Han Peisen, Wang Fang, Zheng Huayu, Chen Xiujian, Meng Hongyu, Li Fenglei
Hua Country People's Hospital, Anyang, 456400, Henan Province, China.
The Department of Computer and Information Engineering, Henan University, Kaifeng, 475001, China.
Sci Rep. 2024 Mar 3;14(1):5200. doi: 10.1038/s41598-024-55808-w.
Systemic sclerosis (SSc), also known as scleroderma, is an autoimmune-related connective tissue disease with a complex and unknown pathophysiological mechanism with genes association. Several articles have reported a high prevalence of thyroid disease in SSc patients, while one study suggested a potential contribution of appendicitis to the development of SSc. To investigate this causal association, we conducted Mendelian randomization (MR) analysis using instrumental variables (IVs) to assess exposure and outcome. In the MR study involving two cohorts, all analyses were conducted using the TwoSampleMR package in R (version 4.3.0). Single nucleotide polymorphisms (SNPs) meeting a statistically significant threshold of 5E-08 were included in the analysis. Multiple complementary approaches including MR-IVW, MR-Egger, weighted median, simple mode, and weighted mode were employed to estimated the relationship between the exposure and outcome. Leave-one-out analysis and scatter plots were utilized for further investigation. Based on the locus-wide significance level, all of the MR analysis consequences manifested no causal association between the risk of appendicitis with SSc (IVW OR 0.319, 95% CI 0.063-14.055, P = 0.966). Negative causal effects of autoimmune thyroiditis (AT) on SSc (IVW OR 0.131, 95% CI 0.816-1.362, P = 0.686), Graves' disease (GD) on SSc (IVW OR 0.097, 95% CI 0.837-1.222, P = 0.908), and hypothyroidism on SSc (IVW OR 1.136, 95% CI 0.977-1.321, P = 0.096) were derived. The reverse MR revealed no significant causal effect of SSc on thyroid disease. According to the sensitivity analysis, horizontal pleiotropy was unlikely to distort the causal estimates. The consequences indicated no significant association between AT, GD, and hypothyroidism with SSc. Similarly, there was no observed relationship with appendicitis.
系统性硬化症(SSc),也称为硬皮病,是一种与自身免疫相关的结缔组织疾病,其病理生理机制复杂且未知,与基因相关。几篇文章报道了SSc患者中甲状腺疾病的高患病率,而一项研究表明阑尾炎可能对SSc的发展有影响。为了研究这种因果关系,我们使用工具变量(IVs)进行孟德尔随机化(MR)分析,以评估暴露因素和结局。在涉及两个队列的MR研究中,所有分析均使用R(版本4.3.0)中的TwoSampleMR软件包进行。分析纳入了达到5E-08统计学显著阈值的单核苷酸多态性(SNP)。采用了多种互补方法,包括MR-IVW、MR-Egger、加权中位数、简单模式和加权模式,来估计暴露因素和结局之间的关系。采用留一法分析和散点图进行进一步研究。基于全基因组显著性水平,所有MR分析结果均表明阑尾炎风险与SSc之间无因果关系(IVW比值比0.319,95%置信区间0.063-14.055,P = 0.966)。自身免疫性甲状腺炎(AT)对SSc的负因果效应(IVW比值比0.131,95%置信区间0.816-1.362,P = 0.686)、格雷夫斯病(GD)对SSc的负因果效应(IVW比值比0.097,95%置信区间0.837-1.222,P = 0.908)以及甲状腺功能减退对SSc的负因果效应(IVW比值比1.136,95%置信区间0.977-1.321,P = 0.096)均被得出。反向MR显示SSc对甲状腺疾病无显著因果效应。根据敏感性分析,水平多效性不太可能扭曲因果估计。结果表明AT、GD和甲状腺功能减退与SSc之间无显著关联。同样,未观察到与阑尾炎的关系。