Experimental Teaching Management Center, Chongqing Medical University, Chongqing, China.
Department of Rheumatology and Immunology, Hainan Hospital of Chinese People's Liberation Army of China (PLA) General Hospital, Sanya, Hainan, China.
Front Immunol. 2024 Feb 8;15:1284466. doi: 10.3389/fimmu.2024.1284466. eCollection 2024.
Despite establishing an association between gut microbiota and spondyloarthritis (SpA) subtypes, the causal relationship between them remains unclear.
Gut microbiota data were obtained from the MiBioGen collaboration, and SpA genome-wide association study (GWAS) summary data were obtained from the FinnGen collaboration. We conducted a two-sample Mendelian randomization (MR) analysis using the inverse-variance-weighted method supplemented with four additional MR methods (MR-Egger, weighted median, simple mode, and weighted mode). Pleiotropy and heterogeneity were also assessed. Reverse MR analysis was used to detect reverse causal relationships.
We identified 23 causal links between specific gut microbiota taxa and SpA levels. Of these, 22 displayed nominal causal associations, and only one demonstrated a robust causal connection. Actinobacteria id.419 increased the risk of ankylosing spondylitis (AS) (odds ratio (OR) = 1.86 (95% confidence interval (CI): 1.29-2.69); = 8.63-04). The family Rikenellaceae id.967 was associated with a reduced risk of both AS (OR = 0.66 (95% CI: 0.47-0.93); = 1.81-02) and psoriatic arthritis (OR = 0.70 (95% CI: 0.50-0.97); = 3.00-02). Bacillales id.1674 increased the risk of AS (OR = 1.23 (95% CI: 1.00-1.51); = 4.94-02) and decreased the risk of enteropathic arthritis (OR = 0.56 (95% CI: 0.35-0.88); = 1.14-02). Directional pleiotropy, or heterogeneity, was not observed. No reverse causal associations were observed between the diseases and the gut microbiota.
Our MR analysis suggested a genetic-level causal relationship between specific gut microbiota and SpA, providing insights into the underlying mechanisms behind SpA development mediated by gut microbiota.
尽管已经确定肠道微生物群与脊柱关节炎(SpA)亚型之间存在关联,但它们之间的因果关系仍不清楚。
肠道微生物组数据来自 MiBioGen 合作,SpA 全基因组关联研究(GWAS)汇总数据来自 FinnGen 合作。我们使用逆方差加权法结合另外四种 MR 方法(MR-Egger、加权中位数、简单模式和加权模式)进行两样本 Mendelian 随机分析。还评估了 pleiotropy 和异质性。反向 MR 分析用于检测反向因果关系。
我们确定了 23 种特定肠道微生物群与 SpA 水平之间的因果关系。其中,22 个显示了名义因果关联,只有一个显示了稳健的因果联系。放线菌 id.419 增加了强直性脊柱炎(AS)的风险(优势比(OR)=1.86(95%置信区间(CI):1.29-2.69); = 8.63-04)。Rikenellaceae 科 id.967 与 AS(OR = 0.66(95% CI:0.47-0.93); = 1.81-02)和银屑病关节炎(OR = 0.70(95% CI:0.50-0.97); = 3.00-02)的风险降低相关。Bacillales id.1674 增加了 AS 的风险(OR = 1.23(95% CI:1.00-1.51); = 4.94-02)和减少了肠病性关节炎的风险(OR = 0.56(95% CI:0.35-0.88); = 1.14-02)。未观察到方向性 pleiotropy 或异质性。疾病与肠道微生物群之间未观察到反向因果关系。
我们的 MR 分析表明,特定肠道微生物群与 SpA 之间存在遗传水平的因果关系,为肠道微生物群介导的 SpA 发展的潜在机制提供了见解。