Cheng Bolun, Wen Yan, Yang Xuena, Cheng Shiqiang, Liu Li, Chu Xiaomeng, Ye Jing, Liang Chujun, Yao Yao, Jia Yumeng, Zhang Feng
Key Laboratory of Trace Elements and Endemic Diseases, Collaborative Innovation Center of Endemic Disease and Health Promotion for Silk Road Region, School of Public Health, Health Science Center, Xi'an Jiaotong University, Xi'an, China.
Key Laboratory for Disease Prevention and Control and Health Promotion of Shaanxi Province, Xi'an, China.
Bone Joint Res. 2021 Nov;10(11):734-741. doi: 10.1302/2046-3758.1011.BJR-2021-0181.R1.
Despite the interest in the association of gut microbiota with bone health, limited population-based studies of gut microbiota and bone mineral density (BMD) have been made. Our aim is to explore the possible association between gut microbiota and BMD.
A total of 3,321 independent loci of gut microbiota were used to calculate the individual polygenic risk score (PRS) for 114 gut microbiota-related traits. The individual genotype data were obtained from UK Biobank cohort. Linear regressions were then conducted to evaluate the possible association of gut microbiota with L1-L4 BMD (n = 4,070), total BMD (n = 4,056), and femur total BMD (n = 4,054), respectively. PLINK 2.0 was used to detect the single-nucleotide polymorphism (SNP) × gut microbiota interaction effect on the risks of L1-L4 BMD, total BMD, and femur total BMD, respectively.
We detected five, three, and seven candidate gut microbiota-related traits for L1-L4 BMD, total BMD, and femur BMD, respectively, such as (p = 0.004) for L1-L4 BMD, and (p = 0.046) for total BMD. We also detected two common gut microbiota-related traits shared by L1-L4 BMD, total BMD, and femur total BMD, including and . Interaction analysis of BMD detected several genes that interacted with gut microbiota, such as phospholipase D1 () and endomucin () interacting with in total BMD, and and Discs Large MAGUK Scaffold Protein 2 () interacting with in femur BMD.
Our results suggest associations between gut microbiota and BMD, which will be helpful to further explore the regulation mechanism and intervention gut microbiota of BMD. Cite this article: 2021;10(11):734-741.
尽管肠道微生物群与骨骼健康之间的关联备受关注,但基于人群的肠道微生物群与骨密度(BMD)的研究却很有限。我们的目的是探讨肠道微生物群与骨密度之间可能存在的关联。
总共使用3321个独立的肠道微生物群基因座来计算114个与肠道微生物群相关性状的个体多基因风险评分(PRS)。个体基因型数据来自英国生物银行队列。然后进行线性回归,分别评估肠道微生物群与L1-L4骨密度(n = 4070)、总骨密度(n = 4056)和股骨总骨密度(n = 4054)之间可能存在的关联。使用PLINK 2.0分别检测单核苷酸多态性(SNP)×肠道微生物群对L1-L4骨密度、总骨密度和股骨总骨密度风险的相互作用效应。
我们分别检测到与L1-L4骨密度、总骨密度和股骨骨密度相关的5个、3个和7个候选肠道微生物群相关性状,例如L1-L4骨密度的(p = 0.004),以及总骨密度的(p = 0.046)。我们还检测到L1-L4骨密度、总骨密度和股骨总骨密度共有的两个常见肠道微生物群相关性状,包括和。骨密度的相互作用分析检测到几个与肠道微生物群相互作用的基因,例如在总骨密度中磷脂酶D1()和内粘蛋白()与相互作用,以及在股骨骨密度中和盘状大MAGUK支架蛋白2()与相互作用。
我们的结果表明肠道微生物群与骨密度之间存在关联,这将有助于进一步探索骨密度的调节机制和干预肠道微生物群。引用本文:2021;10(11):734-741。