Causal relationship between gut microbiota and rosacea: a two-sample Mendelian randomization study

被引:1
作者
Li, Jiaqi [1 ,2 ,3 ]
Yang, Fengjuan [1 ,2 ,3 ]
Liu, Yuling [1 ,2 ,3 ]
Jiang, Xian [1 ,2 ,3 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Dermatol, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, Clin Inst Inflammat & Immunol, Frontiers Sci Ctr Dis Related Mol Network,Lab Derm, Chengdu, Peoples R China
[3] Sichuan Univ, Med X Ctr Informat, Chengdu, Peoples R China
关键词
Mendelian randomization; gut microbiota; rosacea; therapy; dermatology; INTESTINAL BACTERIAL OVERGROWTH; HOST;
D O I
10.3389/fmed.2024.1322685
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Rosacea, a chronic inflammatory skin condition affecting millions worldwide, is influenced by complex interactions between genetic and environmental factors. Although gut microbiota's role in skin health is well-acknowledged, definitive causal links between gut microbiota and rosacea remain under-explored.Methods Using a two-sample Mendelian randomization (MR) design, this study examined potential causal relationships between gut microbiota and rosacea. Data was sourced from the largest Genome-Wide Association Study (GWAS) for gut microbiota and the FinnGen biobank for rosacea. A total of 2078 single nucleotide polymorphisms (SNPs) associated with gut microbiota were identified and analyzed using a suite of MR techniques to discern causal effects.Results The study identified a protective role against rosacea for two bacterial genera: phylum Actinobacteria and genus Butyrivibrio. Furthermore, 14 gut microbiota taxa were discovered to exert significant causal effects on variant categories of rosacea. While none of these results met the strict False Discovery Rate correction threshold, they retained nominal significance. MR outcomes showed no pleiotropy, with homogeneity observed across selected SNPs. Directionality tests pointed toward a robust causative path from gut microbiota to rosacea.Conclusion This study provides compelling evidence of the gut microbiota's nominal causal influence on rosacea, shedding light on the gut-skin axis's intricacies and offering potential avenues for therapeutic interventions in rosacea management. Further research is warranted to validate these findings and explore their clinical implications.
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