Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Jan 31:11:6.
doi: 10.3389/fgene.2020.00006. eCollection 2020.

Assessing the Relationship Between Gut Microbiota and Bone Mineral Density

Affiliations

Assessing the Relationship Between Gut Microbiota and Bone Mineral Density

Shiqiang Cheng et al. Front Genet. .

Abstract

Background: Recent study demonstrates the comprehensive effects of gut microbiota on complex diseases or traits. However, limited effort has been conducted to explore the potential relationships between gut microbiota and BMD.

Methods: We performed a polygenetic risk scoring (PRS) analysis to systematically explore the relationships between gut microbiota and body BMD. Significant SNP sets associated with gut microbiota were derived from previous genome-wide association study (GWAS). In total, 2,294 to 5,065 individuals with BMD values of different sites and their genotype data were obtained from UK Biobank cohort. The gut microbiota PRS of each individual was computed from the SNP genotype data for each study subject of UK Biobank by PLINK software. Using computed PRS as the instrumental variables of gut microbiota, Pearson correlation analysis of individual PRS values and BMD values was finally conducted to test the potential association between gut microbiota and target trait.

Results: In total, 31 BMD traits were selected as outcome to assess their relationships with gut microbiota. After adjusted for age, sex, body mass index, and the first 5 principal components (PCs) as the covariates using linear regression model, pelvis BMD (P = 0.0437) showed suggestive association signal with gut microbiota after multiple testing correction.

Conclusion: Our study findings support the weak relevance of gut microbiota with the development of BMD.

Keywords: bone mineral density; fracture; gut microbiota; osteoporosis; polygenic risk score.

PubMed Disclaimer

Figures

Figure 1
Figure 1
The scatter plot of the adjusted pelvis BMD and gut microbiota PRS.

References

    1. Adamopoulos I. E., Chao C.-C., Geissler R., Laface D., Blumenschein W., Iwakura Y., et al. (2010). Interleukin-17A upregulates receptor activator of NF-κB on osteoclast precursors. Arthritis Res. Ther. 12 (1), R29. 10.1186/ar2936 - DOI - PMC - PubMed
    1. Burge R., Dawson-Hughes B., Solomon D. H., Wong J. B., King A., Tosteson A. (2007). Incidence and economic burden of osteoporosis-related fractures in the United States, 2005–2025. J. Bone Miner. Res. 22 (3), 465–475. 10.1359/jbmr.061113 - DOI - PubMed
    1. Bycroft C., Freeman C., Petkova D., Band G., Elliott L. T., Sharp K., et al. (2017). Genome-wide genetic data on ~500,000 UK Biobank participants. bioRxiv 166298. 10.1101/166298 - DOI
    1. Bycroft C., Freeman C., Petkova D., Band G., Elliott L. T., Sharp K., et al. (2018). The UK Biobank resource with deep phenotyping and genomic data. Nature 562 (7726), 203–209. 10.1038/s41586-018-0579-z - DOI - PMC - PubMed
    1. Canela-Xandri O., Rawlik K., Tenesa A. (2018). An atlas of genetic associations in UK Biobank. Nat. Genet. 50 (11), 1593–1599. 10.1038/s41588-018-0248-z - DOI - PMC - PubMed

LinkOut - more resources