Evidence map›Paper›PMID 39375626›Full record

ArticleBMC musculoskeletal disorders2024

Osteoporosis in postmenopausal women is associated with disturbances in gut microbiota and migration of peripheral immune cells.

Zongjun Ma, Yuanyuan Liu, Wenke Shen, Jiaxiao Yang, Ting Wang, Yiwei Li, Junbai Ma, Xiaoxia Zhang, Hao Wang

Abstract read
In one paragraph

Article in BMC musculoskeletal disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

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

  1. Pooled it
  2. Review
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  5. The gut-bone-inflammation axis: intestinal barrier disruption as a central driver of osteoporosis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2026
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  8. Aging-Driven Inter-Organ Crosstalk in Postmenopausal Osteoporosis: From Immunometabolic Drift to Multisystem Frailty.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
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  12. Periodontal Disease and Osteoporosis: A Bidirectional Relationship.Advances in experimental medicine and biology · 2026
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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

9 authors.

Zongjun Ma *General Hospital of Ningxia Medical University, Yinchuan, 750004, Ningxia, China.
Yuanyuan Liu *School of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, Ningxia, China.
Wenke ShenSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, Ningxia, China.
Jiaxiao YangSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, Ningxia, China.
Ting WangSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, Ningxia, China.
Yiwei LiSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, Ningxia, China.
Junbai MaSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, Ningxia, China.
Xiaoxia ZhangCollege of Traditional Chinese Medicine, Ningxia Medical University, Yinchuan, 750004, Ningxia, China. zxx1216@163.com.
Hao WangSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, Ningxia, China. wanghaograduate@126.com.

Funding

Category B: Tennessee Pregnancy Risk Assessment Monitoring SystemU01DP003112 · DP · TENNESSEE STATE DEPARTMENT OF HEALTH · PI LAINHART, RAMONA I · 2011 to 2015
$617k
the Key Research and Development Program of Ningxia, China Grant No. 2023BEG02011the National Natural Science Foundation of China Grant No. 82160691the National Natural Science Foundation of China Grant No. 82260800the Ningxia Gut Homeostasis and Chronic Disease Prevention and Treatment Scientific and Technological Innovation Team, China Grant No. 2022BSB03112the Ningxia Natural Science Foundation, China Grant No. 2020AAC03396
6 · The paper itself

Abstract

backgroundPostmenopausal osteoporosis (PMO) results from a reduction in bone mass and microarchitectural deterioration in bone tissue due to estrogen deficiency, which may increase the incidence of fragility fractures. In recent years, the "gut-immune response-bone" axis has been proposed as a novel potential approach in the prevention and treatment of PMO. Studies on ovariectomized murine model indicated the reciprocal role of Th17 cells and Treg cells in the aetiology of osteoporosis. However, the relationship among gut microbiota, immune cells and bone metabolic indexes remains unknown in PMO.

methodsA total of 77 postmenopausal women were recruited for the study and divided into control (n = 30), osteopenia (n = 19), and osteoporosis (n = 28) groups based on their T score. The frequency of Treg and Th17 cells in lymphocytes were analyzed by flow cytometry. The serum levels of interleukin (IL)-10, 17 A, 1β, 6, tumor necrosis factor (TNF)-α, and lipopolysaccharide (LPS) were determined via enzyme-linked immunosorbent assay. Additionally, 16S rRNA gene V3-V4 region sequencing analysis was performed to investigate the gut microbiota of the participants.

resultsThe results demonstrated decreased bacterial richness and diversed intestinal composition in PMO. In addition, significant differences of relative abundance of the gut microbial community in phylum and genus levels were found, mainly including increased Bacteroidota, Proteobacteria, and Campylobacterota, as well as reduced Firmicutes, Butyricicoccus, and Faecalibacterium. Intriugingly, in the osteoporosis group, the concentration of Treg cells and associated IL-10 in peripheral circulation was negatively regulated, while other chronic systemic proinflammatory cytokines and Th17 cells showed opposite trends. Moreover, significantly elevated plasma lipopolysaccharide (LPS) in patients with osteoporosis indicated that disrupted intestinal integrity and permeability. A correlation analysis showed close relationships between gut bacteria and inflammation.

conclusionsCollectively, these observations will lead to a better understanding of the relationship among bone homeostasis, the microbiota, and circulating immune cells in PMO. The elevated LPS levels of osteoporosis patients which not only indicate a breach in intestinal integrity but also suggest a novel biomarker for assessing osteoporosis risk linked to gut health.

Indexed as

Gastrointestinal MicrobiomeOsteoporosis, PostmenopausalTh17 CellsT-Lymphocytes, RegulatoryAgedCell MovementCytokinesFemaleHumansMiddle AgedPostmenopauseCytokinesGut microbiotaInflammation cytokinesLipopolysaccharide (LPS)Postmenopausal osteoporosis (PMO)Regulatory T cells (Treg)T helper cell 17 (Th17)

Identifiers

PMID39375626
PMCPMC11460084

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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.