肠道菌群与骨质疏松性骨折  

Gut microbiota and osteoporotic fractures

作　　者：赵文生 李孝林[2] 彭昌华[3] 邓佳 盛浩 陈洪卫[3] 张朝驹 何川[1,3] Zhao Wensheng;Li Xiaolin;Peng Changhua;Deng Jia;Sheng Hao;Chen Hongwei;Zhang Chaoju;He Chuan(Hubei University of Chinese Medicine,Wuhan 430061,Hubei Province,China;Yangtze University,Jingzhou 434023,Hubei Province,China;Jingzhou Hospital of Traditional Chinese Medicine Affiliated to Hubei University of Chinese Medicine,Jingzhou 434000,Hubei Province,China)

机构地区：[1]湖北中医药大学,湖北省武汉市430061 [2]长江大学,湖北省荆州市434023 [3]湖北中医药大学附属荆州市中医医院,湖北省荆州市434000

出　　处：《中国组织工程研究》2025年第6期1296-1304,共9页Chinese Journal of Tissue Engineering Research

基　　金：全国名老中医专家传承工作室建设项目(国中医药人教函[2022]75号),项目负责人:张朝驹;湖北省自然科学基金面上项目(2022CFB054),项目负责人:李孝林;湖北省中医药管理局中医药科研面上项目(ZY2023M051),项目负责人:何川;荆州市中医药研究所自主选题项目(ZZXT2023Y07),项目负责人:彭昌华。

摘　　要：背景:骨质疏松性骨折是骨质疏松症最严重的并发症,既往的研究已经证实了肠道菌群对骨骼组织具有调节作用,肠道菌群与骨质疏松性骨折有着重要关系,但是二者之间的因果关系尚不清楚。目的:使用孟德尔随机化(MR)方法探索肠道菌群与骨质疏松性骨折之间的因果关系。方法:从IEU Open GWAS数据库和芬兰数据库R9中分别获得了肠道菌群和骨质疏松性骨折的GWAS数据集,以肠道菌群作为暴露因素,骨质疏松性骨折作为结局变量,采用随机效应逆方差加权法、MR-Egger回归、加权中位数法、简单模型法以及加权模型法进行孟德尔随机化分析来评估肠道菌群与骨质疏松性骨折之间是否存在因果关系,通过敏感性分析来检验结果的可靠性和稳健性,并进行反向孟德尔随机化分析来进一步验证正向孟德尔随机化分析中确定的因果关系。结果与结论:①此孟德尔随机化分析结果表明,肠道菌群与骨质疏松性骨折之间存在因果关系。放线菌目(OR=1.562,95%CI:1.027-2.375,P=0.037)、放线菌科(OR=1.561,95%CI:1.027-2.374,P=0.037)、放线菌属(OR=1.544,95%CI:1.130-2.110,P=0.006)、丁酸球菌属(OR=1.781,95%CI:1.194-2.657,P=0.005)、粪球菌属-2(OR=1.550,95%CI:1.068-2.251,P=0.021)、Family ⅩⅢ UCG-001属(OR=1.473,95%CI:1.001-2.168,P=0.049)、产甲烷短杆菌属(OR=1.274,95%CI:1.001-1.621,P=0.049)、罗氏菌属(OR=1.429,95%CI:1.015-2.013,P=0.041)的丰度升高,会增加患者骨质疏松性骨折的风险;②拟杆菌纲(OR=0.660,95%CI:0.455-0.959,P=0.029)、拟杆菌目(OR=0.660,95%CI:0.455-0.959,P=0.029)、克里斯滕森氏菌科(OR=0.725,95%CI:0.529-0.995,P=0.047)、瘤胃球菌科(OR=0.643,95%CI:0.443-0.933,P=0.020)、肠杆菌属(OR=0.558,95%CI:0.395-0.788,P=0.001)、直肠真杆菌属(OR=0.631,95%CI:0.435-0.916,P=0.016)、毛螺菌科-UCG008(OR=0.738,95%CI:0.546-0.998,P=0.048)、瘤胃梭菌属-9(OR=0.492,95%CI:0.324-0.746,P=0.001)的丰度升高,会降低患者骨质疏松性�BACKGROUND:Osteoporotic fracture is the most serious complication of osteoporosis.Previous studies have demonstrated that gut microbiota has a regulatory effect on skeletal tissue and that gut microbiota has an important relationship with osteoporotic fracture,but the causal relationship between the two is unclear.OBJECTIVE:To explore the causal relationship between gut microbiota and osteoporotic fractures using Mendelian randomization method.METHODS:The genome-wide association study(GWAS)datasets of gut microbiota and osteoporotic fracture were obtained from the IEU Open GWAS database and the Finnish database R9,respectively.Using gut microbiota as the exposure factor and osteoporotic fracture as the outcome variable,Mendelian randomization analyses with random-effects inverse variance weighted,MR-Egger regression,weighted median,simple model,and weighted model methods were performed to assess whether there is a causal relationship between gut microbiota and osteoporotic fracture.Sensitivity analyses were performed to test the reliability and robustness of the results.Reverse Mendelian randomization analyses were performed to further validate the causal relationship identified in the forward Mendelian randomization analyses.RESULTS AND CONCLUSION:The results of this Mendelian randomization analysis indicated a causal relationship between gut microbiota and osteoporotic fracture.Elevated abundance of Actinomycetales[odds ratio(OR)=1.562,95%confidence interval(CI):1.027-2.375,P=0.037],Actinomycetaceae(OR=1.561,95%CI:1.027-2.374,P=0.037),Actinomyces(OR=1.544,95%CI:1.130-2.110,P=0.006),Butyricicoccus(OR=1.781,95%CI:1.194-2.657,P=0.005),Coprococcus 2(OR=1.550,95%CI:1.068-2.251,P=0.021),Family ⅩⅢ UCG-001(OR=1.473,95%CI:1.001-2.168,P=0.049),Methanobrevibacter(OR=1.274,95%CI:1.001-1.621,P=0.049),and Roseburia(OR=1.429,95%CI:1.015-2.013,P=0.041)would increase the risk of osteoporotic fractures in patients.Elevated abundance of Bacteroidia(OR=0.660,95%CI:0.455-0.959,P=0.029),Bacteroidales(OR=0.660,95%CI:0.455-0.959,P

关 键 词：孟德尔随机化 肠道菌群 骨质疏松性骨折 因果关系 遗传学 全基因组关联研究 单核苷酸多态性 工具变量 风险因素 

分 类 号：R459.9[医药卫生—治疗学] R318[医药卫生—临床医学] R452