Xiong Yujun, Zhu Xingyun, Luo Qingfeng
Department of Gastroenterology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, PR China, 100370, Beijing, China.
Department of Endocrinology, Beijing Jishuitan Hospital, No. 31, East Xinjiekou Street, Xicheng District, 100035, Beijing, China.
Heliyon. 2024 Feb 6;10(3):e25652. doi: 10.1016/j.heliyon.2024.e25652. eCollection 2024 Feb 15.
Autoimmune thyroiditis (AIT), also known as Hashimoto's thyroiditis (HT) or chronic lymphocytic thyroiditis, is a prevalent autoimmune disorder. Despite its high prevalence, the pathogenesis of AIT remains unclear. Previous studies have suggested a potential association between gut microbiota and AIT. However, whether this relationship is causal or coincidental remains uncertain. To address this gap in knowledge, our study aimed to investigate the potential causal association between gut microbiota and AIT using the two-sample Mendelian randomization (MR) method.
Summary-level gut microbiota data comprising 211 taxa (131 genera, 35 families, 20 orders, 16 classes, and 9 phyla) were obtained from the comprehensive MiBioGen study. Genetic associations with 22 gastrointestinal diseases were extracted from the UK Biobank, FinnGen study, and various extensive GWAS studies. A meticulous MR analysis was conducted to evaluate the causal relationship between genetically predicted gut microbiota and these gastrointestinal diseases. Sensitivity analyses and tests for heterogeneity were systematically performed to validate the reliability of our findings.
Six gut microbiota species showed significant associations with AIT according to the IVW method. Among them, the following exhibited negative associations with AIT: family Alcaligenaceae, family Pasteurellaceae (ID: 3689), family Peptococcaceae, genus Lachnospira, genus Victivallis, and order Pasteurellales (ID: 3688). No evidence of pleiotropy or heterogeneity was detected.
The MR analysis uncovered a causal relationship at the genetic prediction level between specific gut microbiota and AIT. These findings offer novel insights into the mechanisms governing the development of AIT mediated by gut microbiota. This knowledge could inform the design of future interventions, potentially involving microbiome-related strategies, to address the mechanisms associated with AIT development.
自身免疫性甲状腺炎(AIT),也称为桥本甲状腺炎(HT)或慢性淋巴细胞性甲状腺炎,是一种常见的自身免疫性疾病。尽管其患病率很高,但AIT的发病机制仍不清楚。先前的研究表明肠道微生物群与AIT之间可能存在关联。然而,这种关系是因果关系还是巧合仍不确定。为了填补这一知识空白,我们的研究旨在使用两样本孟德尔随机化(MR)方法研究肠道微生物群与AIT之间的潜在因果关联。
从全面的MiBioGen研究中获得了包含211个分类单元(131个属、35个科、20个目、16个纲和9个门)的汇总水平肠道微生物群数据。从英国生物银行、芬兰基因研究和各种广泛的全基因组关联研究(GWAS)中提取了与22种胃肠道疾病的遗传关联。进行了细致的MR分析,以评估基因预测的肠道微生物群与这些胃肠道疾病之间的因果关系。系统地进行了敏感性分析和异质性检验,以验证我们研究结果的可靠性。
根据逆方差加权(IVW)方法,六种肠道微生物物种与AIT存在显著关联。其中,以下与AIT呈负相关:产碱菌科、巴斯德菌科(ID:3689)、消化球菌科、毛螺菌属、Victivallis属和巴斯德菌目(ID:3688)。未检测到多效性或异质性的证据。
MR分析在基因预测水平上揭示了特定肠道微生物群与AIT之间的因果关系。这些发现为肠道微生物群介导的AIT发展机制提供了新的见解。这些知识可为未来干预措施的设计提供参考,可能涉及与微生物组相关的策略,以解决与AIT发展相关的机制。