Yao Y, Chen J, Cao H, Lu Z, Shen H, Ji J, Jiao Q
Department of Dermatology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Central Research Laboratory, The First Affiliated Hospital of Soochow University, Suzhou, China.
J Investig Allergol Clin Immunol. 2025 Feb 6:0. doi: 10.18176/jiaci.1054.
To analyze causality between gut microbiota and chronic spontaneous urticaria (CSU) and to investigate the mediating effect of metabolic pathways.
We extracted genome-wide association study summary statistics for 211 microbiota taxa from the MiBioGen consortium (N=18 340), 205 microbiota metabolic pathways from the Dutch Microbiome Project (N=7738), and CSU from the FinnGen genomics initiative (N=450). Bidirectional Mendelian randomization (MR) was performed to detect genetic causality between gut microbiota, gut bacterial pathways, and CSU. Sensitivity analyses were performed to validate the robustness of the results. Mediation MR investigated mediators in the association between gut microbiota and CSU.
MR analysis suggested that the family Peptococcaceae and its child taxon, the genus Peptococcus, were risk factors for CSU. In addition, the genera Collinsella, Lachnospiraceae UCG004, Ruminococcaceae UCG004, and Sellimonas were also risk factors for CSU, whereas Family XIII UCG001, Lachnospiraceae UCG010, and Methanobrevibacter had protective effects on CSU. As for metabolic pathways, NONMEVIPP-PWY, PWY-5022, and PWY-7221 were positively associated with CSU, although others, such as KDO-NAGLIPASYN-PWY, PWY- 6353, and PWY-7400 presented a suggestive association with CSU. Moreover, PWY-7400 was a mediator in causality between the family Peptococcaceae and CSU. These results were based on nominal significance (P<.05). None of the Bonferroni corrected P values were <.05.
Our study confirmed a causal association between gut microbiota and CSU, with the metabolic pathway being a potential mediator. Our findings provide new insights for further mechanistic and clinical studies in CSU.
分析肠道微生物群与慢性自发性荨麻疹(CSU)之间的因果关系,并研究代谢途径的中介作用。
我们从MiBioGen联盟(N = 18340)中提取了211种微生物分类群的全基因组关联研究汇总统计数据,从荷兰微生物组计划(N = 7738)中提取了205种微生物代谢途径的数据,以及从芬兰基因组计划(N = 450)中提取了CSU的数据。进行双向孟德尔随机化(MR)以检测肠道微生物群、肠道细菌途径与CSU之间的遗传因果关系。进行敏感性分析以验证结果的稳健性。中介MR研究了肠道微生物群与CSU之间关联的中介因素。
MR分析表明,消化球菌科及其子分类群消化球菌属是CSU的危险因素。此外,柯林斯菌属、毛螺菌科UCG004、瘤胃球菌科UCG004和Sellimonas属也是CSU的危险因素,而XIII科UCG001、毛螺菌科UCG010和甲烷短杆菌对CSU有保护作用。至于代谢途径,NONMEVIPP-PWY、PWY-5022和PWY-7221与CSU呈正相关,尽管其他途径,如KDO-NAGLIPASYN-PWY、PWY-6353和PWY-7400与CSU存在提示性关联。此外,PWY-7400是消化球菌科与CSU因果关系的中介因素。这些结果基于名义显著性(P <.05)。经Bonferroni校正后,所有P值均不小于.05。
我们的研究证实了肠道微生物群与CSU之间存在因果关联,代谢途径是潜在的中介因素。我们的研究结果为CSU的进一步机制和临床研究提供了新的见解。