Evidence map›Paper›PMID 40000617›Full record

ArticleBone research2025

Bifidobacterium animalis subsp. lactis A6 ameliorates bone and muscle loss via modulating gut microbiota composition and enhancing butyrate production.

Ming Chen, Yi Li, Zhengyuan Zhai, Hui Wang, Yuan Lin, Feifan Chang, Siliang Ge, Xinyu Sun, Wei Wei, Duanyang Wang and 11 more

Abstract read
In one paragraph

Article in Bone research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–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

31 citing papers in PubMed.

  1. Review
  2. Article
  3. Hesperetin mitigates IBD-associated bone loss viaJournal of orthopaedic translation · 2026
    Article
  4. Review
  5. Article
  6. Links between bone fractures and the gut microbiota.Nature reviews. Endocrinology · 2026
    Review
  7. Review
  8. Phenylethanoid Glycosides fromInternational journal of molecular sciences · 2026
    Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Nutrients · 2026
    Article
  15. Article
  16. Regulating the crosstalk betweenFrontiers in immunology · 2026
    Review
  17. Indole derivatives intervene osteoporosis via gut-bone axis.Frontiers in cellular and infection microbiology · 2026
    Review
  18. Review
  19. Review
  20. Review
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

21 authors.

Ming Chen *Senior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.
Yi Li *Senior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.
Zhengyuan ZhaiKey Laboratory of Precision Nutrition and Food Quality, Department of Nutrition and Health, China Agricultural University, Beijing, China.
Hui WangKey Laboratory of Precision Nutrition and Food Quality, Department of Nutrition and Health, China Agricultural University, Beijing, China.
Yuan LinThe Department of Orthopedic Surgery, Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Feifan ChangSenior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.
Siliang GeSenior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.
Xinyu SunSenior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.
Wei WeiDepartment of Clinical Nutrition, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
Duanyang WangThe Department of Orthopedic Surgery, Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Mingming ZhangSenior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.
Ruijing ChenSenior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.
Haikuan YuSenior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.
Taojin FengSenior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.
Xiang HuangSenior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.
Dongliang ChengSenior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.
Jiang LiuThe Department of Orthopedic Surgery, Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Wenxuan DiKey Laboratory of Precision Nutrition and Food Quality, Department of Nutrition and Health, China Agricultural University, Beijing, China.
Yanling HaoKey Laboratory of Precision Nutrition and Food Quality, Department of Nutrition and Health, China Agricultural University, Beijing, China. haoyl@cau.edu.cn.
Pengbin YinSenior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China. yinpengbin@gmail.com.ORCID http://orcid.org/0000-0002-5391-4477
Peifu TangSenior Department of Orthopedics, The Fourth Medical Center of Chinese PLA General Hospital, Beijing, China.ORCID http://orcid.org/0000-0003-4279-1704

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82202728
6 · The paper itself

Abstract

Systematic bone and muscle loss is a complex metabolic disease, which is frequently linked to gut dysfunction, yet its etiology and treatment remain elusive. While probiotics show promise in managing diseases through microbiome modulation, their therapeutic impact on gut dysfunction-induced bone and muscle loss remains to be elucidated. Employing dextran sulfate sodium (DSS)-induced gut dysfunction model and wide-spectrum antibiotics (ABX)-treated mice model, our study revealed that gut dysfunction instigates muscle and bone loss, accompanied by microbial imbalances. Importantly, Bifidobacterium animalis subsp. lactis A6 (B. lactis A6) administration significantly ameliorated muscle and bone loss by modulating gut microbiota composition and enhancing butyrate-producing bacteria. This intervention effectively restored depleted butyrate levels in serum, muscle, and bone tissues caused by gut dysfunction. Furthermore, butyrate supplementation mitigated musculoskeletal loss by repairing the damaged intestinal barrier and enriching beneficial butyrate-producing bacteria. Importantly, butyrate inhibited the NF-κB pathway activation, and reduced the secretion of corresponding inflammatory factors in T cells. Our study highlights the critical role of dysbiosis in gut dysfunction-induced musculoskeletal loss and underscores the therapeutic potential of B. lactis A6. These discoveries offer new microbiome directions for translational and clinical research, providing promising strategies for preventing and managing musculoskeletal diseases.

Indexed as

Bifidobacterium animalisButyratesGastrointestinal MicrobiomeAnimalsDextran SulfateMaleMiceMice, Inbred C57BLProbioticsButyratesDextran Sulfate

Identifiers

PMID40000617
PMCPMC11862215

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Registered trials

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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.