Evidence map›Paper›PMID 38883609›Full record

ArticleFrontiers in endocrinology2024

Gut-bone axis research: unveiling the impact of gut microbiota on postmenopausal osteoporosis and osteoclasts through Mendelian randomization.

Hefang Xiao, Yaobin Wang, Yi Chen, Rongjin Chen, Chenhui Yang, Bin Geng, Yayi Xia

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  14. Gut-Adipose Tissue Axis and Metabolic Health.Current issues in molecular biology · 2025
    Review
  15. Cross-talks between osteoporosis and gut microbiome.World journal of orthopedics · 2025
    Review
  16. Article
  17. Frontiers in nutrition · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Hefang Xiao *Department of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, China.
Yaobin Wang *Department of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, China.
Yi Chen *Department of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, China.
Rongjin ChenDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, China.
Chenhui YangDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, China.
Bin GengDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, China.
Yayi XiaDepartment of Orthopaedics, Lanzhou University Second Hospital, Lanzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Postmenopausal osteoporosis is a prevalent disease that affects the bone health of middle-aged and elderly women. The link between gut microbiota and bone health, known as the gut-bone axis, has garnered widespread attention. Methods: We employed a two-sample Mendelian randomization approach to assess the associations between gut microbiota with osteoclasts and postmenopausal osteoporosis, respectively. Single nucleotide polymorphisms associated with the composition of gut microbiota were used as instrumental variables. By analyzing large-scale multi-ethnic GWAS data from the international MiBioGen consortium, and combining data from the eQTLGen consortium and the GEFOS consortium, we identified microbiota related to osteoclasts and postmenopausal osteoporosis. Key genes were further identified through MAGMA analysis, and validation was performed using single-cell data GSE147287. Results: The outcomes of this study have uncovered significant associations within the gut microbiome community, particularly with the Burkholderiales order, which correlates with both an increase in osteoclasts and a reduced risk of postmenopausal osteoporosis. with an odds ratio (OR) of 0.400, and a P-value of 0.011. Further analysis using single-cell data allowed us to identify two key genes, FMNL2 and SRBD1, that are closely linked to both osteoclasts and osteoporosis. Conclusion: This study utilizing Mendelian randomization and single-cell data analysis, provides new evidence of a causal relationship between gut microbiota and osteoclasts, as well as postmenopausal osteoporosis. It was discovered that the specific microbial group, the Burkholderiales order, significantly impacts both osteoporosis and osteoclasts. Additionally, key genes FMNL2 and SRBD1 were identified, offering new therapeutic strategies for the treatment of postmenopausal osteoporosis.

Indexed as

Gastrointestinal MicrobiomeGenome-Wide Association StudyMendelian Randomization AnalysisOsteoclastsOsteoporosis, PostmenopausalPolymorphism, Single NucleotideAgedBone and BonesFemaleHumansMiddle Agedgut-bone axisgut microbiotaGWASMendelian randomizationosteoclastspostmenopausal osteoporosis

Identifiers

PMID38883609
PMCPMC11176613

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.