Cai Yong, Zhou Chaoqing, Guan Junjie, Dai Bo, Zhang Xingshi, Jiang Jizhao, Zhao Jun
Department of Orthopaedics, Xishui County People's Hospital, Across from Hongding Community, Zunyi City, Guizhou Province, China.
Department of Orthopaedics, Zhuhai Hospital of Integrated Traditional Chinese and Western Medicine, Zhuhai, Guangdong, China.
Medicine (Baltimore). 2025 Mar 7;104(10):e41703. doi: 10.1097/MD.0000000000041703.
Emerging evidence indicates an association between the gut microbiota and the incidence of osteonecrosis (ON), yet the literature has not adequately addressed whether this relationship is causal. This study uses data from the MiBioGen Consortium and the UK Biobank for Mendelian randomization (MR) analysis to identify pathogenic gut microbial taxa associated with ON. Sensitivity analyses confirmed causal relationships, while reverse MR ruled out reverse causation. SNP annotation located genetic variants linked to gut microbiota instrumental variables in ON. The inverse variance weighted method revealed 5 microbial taxa with a causal association with ON, including the order Erysipelotrichales (OR = 2.24, 95% CI = 1.16-4.32, P = .02), genus Christensenellaceae R (OR = 0.41, 95% CI = 0.19-0.87, P = .02), family Erysipelotrichaceae (OR = 2.24, 95% CI = 1.16-4.32, P = .02), family Family XIII (OR = 0.45, 95% CI = 0.21-0.95, P = .04), and class Erysipelotrichia (OR = 2.24, 95% CI = 1.16-4.32, P = .02). Sensitivity analyses mitigated concerns regarding heterogeneity, directional pleiotropy, and outliers (P > .05). However, the reverse MR showed no causal effect of ON on these taxa. SNP (single-nucleotide polymorphism) annotation pinpointed 20 host genes associated with ON pathogenesis. These findings lay the groundwork for microbiota-targeted therapies and deepen our understanding of the gut-bone axis in osteonecrosis.
新出现的证据表明肠道微生物群与骨坏死(ON)的发病率之间存在关联,但文献尚未充分探讨这种关系是否为因果关系。本研究使用来自MiBioGen联盟和英国生物银行的数据进行孟德尔随机化(MR)分析,以确定与ON相关的致病性肠道微生物分类群。敏感性分析证实了因果关系,而反向MR排除了反向因果关系。SNP注释确定了与ON中肠道微生物群工具变量相关的基因变异。逆方差加权法揭示了5个与ON有因果关联的微生物分类群,包括丹毒丝菌目(OR = 2.24,95%CI = 1.16 - 4.32,P = 0.02)、克里斯滕森菌科R属(OR = 0.41,95%CI = 0.19 - 0.87,P = 0.02)、丹毒丝菌科(OR = 2.24,95%CI = 1.16 - 4.32,P = 0.02)、第十三科(OR = 0.45,95%CI = 0.21 - 0.95,P = 0.04)和丹毒丝菌纲(OR = 2.24,95%CI = 1.16 - 4.32,P = 0.02)。敏感性分析减轻了对异质性、定向多效性和异常值的担忧(P > 0.05)。然而,反向MR显示ON对这些分类群没有因果效应。SNP(单核苷酸多态性)注释确定了20个与ON发病机制相关的宿主基因。这些发现为以微生物群为靶点的治疗奠定了基础,并加深了我们对骨坏死中肠骨轴的理解。