Gut microbiota, skin microbiota, and alopecia areata: A Mendelian randomization study

斑秃 孟德尔随机化 优势比 置信区间 肠道菌群 内科学 棒状杆菌 医学 胃肠病学 皮肤病科 生物 免疫学 遗传学 细菌 基因型 基因 遗传变异
作者
Zishun Li,Changpu Zhao,R Chen,Meiling Li,Fei Wang,Chenyuan Hao,Rongzhi Li,Yu Zhang,Yuying Xu
出处
期刊:Skin Research and Technology [Wiley]
卷期号:30 (7) 被引量:3
标识
DOI:10.1111/srt.13845
摘要

Abstract Background Observational studies have shown an association between skin microbiota and alopecia areata (AA), but the causal connection remains ambiguous. Methods We obtained data on skin microbiota and AA from summary statistics of Genome‐Wide Association Studies and applied statistical methods from Mendelian randomization (MR) to assess causal relationships. Additionally, we investigated whether the skin microbiota acts as a mediator in the pathway from gut microbiota to AA. Results In the MR analysis of KORA FF4 and AA, the inverse‐variance weighting method indicated that Corynebacterium (odds ratio [OR] = 0.82, 95% confidence interval [CI]: 0.70–0.96, p = 0.02) and asv037 (OR = 0.87, 95% CI: 0.76–0.99, p = 0.05) exerted protective effects, while Betaproteobacteria (OR = 1.21, 95% CI: 1.01–1.44, p = 0.03), asv015 (OR = 1.27, 95% CI: 1.05–1.54, p = 0.02), and Burkholderiales (OR = 1.20, 95% CI: 1.04–1.38, p = 0.01) were identified as risk factors in AA. In the MR analysis of PopGen and AA, asv001 (OR = 1.12, 95% CI: 1.01–1.24, p = 0.04), asv054 (OR = 1.13, 95% CI: 1.01–1.25, p = 0.03), and asv059 (OR = 1.14, 95% CI: 1.02–1.27, p = 0.02) were found to potentially increase the risk in AA. Furthermore, in the influence of gut microbiota on AA, the skin microbiota did not act as a mediator. Conclusion Our analysis suggests potential causal relationships between certain skin microbiota and AA, revealing insights into its pathogenesis and potential intervention strategies.

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