Evidence map›Paper›PMID 39348436›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2024

Microbiome-induced increases and decreases in bone matrix strength can be initiated after skeletal maturity.

Chongshan Liu, Erika L Cyphert, Samuel J Stephen, Bowen Wang, Angie L Morales, Jacob C Nixon, Nicholas R Natsoulas, Matthew Garcia, Pablo Blazquez Carmona, Albert C Vill and 4 more

Abstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Links between bone fractures and the gut microbiota.Nature reviews. Endocrinology · 2026
    Review
  2. Bone Fragility: Time to Address the Matrix.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2026
    Article
  3. Gut microbiome-dependent IL-1 signaling is a mediator of ACVR1bioRxiv : the preprint server for biology · 2026
    Article
  4. Dysbiosis in the Gut-Liver Axis Is Associated With Low Bone Mass During Murine Cholestasis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Chongshan LiuDepartments of Orthopaedic Surgery and Bioengineering and Therapeutic Sciences, University of California, San Francisco, CA, United States.
Erika L CyphertDepartments of Orthopaedic Surgery and Bioengineering and Therapeutic Sciences, University of California, San Francisco, CA, United States.
Samuel J StephenShirley Ann Jackson, PhD Center for Biotechnology and Interdisciplinary Studies, Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY, United States.
Bowen WangShirley Ann Jackson, PhD Center for Biotechnology and Interdisciplinary Studies, Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY, United States.
Angie L MoralesSibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, United States.
Jacob C NixonSibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, United States.
Nicholas R NatsoulasSibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, United States.
Matthew GarciaSibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, United States.
Pablo Blazquez CarmonaEscuela Superior de Ingeniería, Universidad de Cádiz, Spain.
Albert C VillMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, United States.
Eve DonnellyDepartment of Material Science and Engineering, Cornell University, Ithaca, NY, United States.
Ilana L BritoMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, United States.
Deepak VashishthShirley Ann Jackson, PhD Center for Biotechnology and Interdisciplinary Studies, Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY, United States.
Christopher J HernandezDepartments of Orthopaedic Surgery and Bioengineering and Therapeutic Sciences, University of California, San Francisco, CA, United States.ORCID 0000-0002-0712-6533

Funding

Skeletal Biology and Biomechanics (SBB) CoreP30AR075055 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Wenhan Chang · 2019 to 2026
$7.1M
The Microbiome and Bone StrengthR01AG067997 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HERNANDEZ, CHRISTOPHER JOHN · 2021 to 2025
$3.2M
The Microbiome and Bone StrengthR56AG067997 · NIA · CORNELL UNIVERSITY · PI HERNANDEZ, CHRISTOPHER JOHN · 2020 to 2020
$597k
Gut microbial factors that increase bone tissue strengthF32AG076244 · NIA · CORNELL UNIVERSITY · PI CYPHERT, ERIKA LEAH · 2022 to 2023
$127k
NIAMS NIH HHS P30 AR075055NIA NIH HHS F32 AG076244NIA NIH HHS R01 AG067997NIA NIH HHS R56 AG067997NIHNIH HHS F32AG076244
6 · The paper itself

Abstract

Recent studies in mice have indicated that the gut microbiome can regulate bone tissue strength. However, prior work involved modifications to the gut microbiome in growing animals and it is unclear if the same changes in the microbiome, applied later in life, would change matrix strength. Here we changed the composition of the gut microbiome before and/or after skeletal maturity (16 weeks of age) using oral antibiotics (ampicillin + neomycin). Male and female mice (n = 143 total, n = 12-17/group/sex) were allocated into five study groups: (1) Unaltered, (2) Continuous (dosing 4-24 weeks of age), (3) Delayed (dosing only 16-24 weeks of age), (4) Initial (dosing 4-16 weeks of age, suspended at 16 weeks), and (5) Reconstituted (dosing from 4-16 weeks following by fecal microbiota transplant from Unaltered donors). Animals were euthanized at 24 weeks of age. In males, bone matrix strength in the femur was 25%-35% less than expected by geometry in mice from the Continuous (p = 0.001), Delayed (p = 0.005), and Initial (p = 0.040) groups as compared to Unaltered. Reconstitution of the gut microbiota led to a bone matrix strength similar to Unaltered animals (p = 0.929). In females, microbiome-induced changes in bone matrix strength followed the same trend as males but were not significantly different, demonstrating a sex-dependent response of bone matrix to the gut microbiota. Minor differences in chemical composition of bone matrix were observed with Raman spectroscopy. Our findings indicate that microbiome-induced impairment of bone matrix in males can be initiated and/or reversed after skeletal maturity. The portion of the femoral cortical bone formed after skeletal maturity (16 weeks) was small; suggesting that microbiome-induced changes in bone matrix occurred without osteoblast/osteoclast turnover through a yet unidentified mechanism. These findings provide evidence that the mechanical properties of bone matrix can be altered in the adult skeleton.

Indexed as

FemurGastrointestinal MicrobiomeAnimalsBone MatrixFemaleMaleMiceMice, Inbred C57BLbiomechanicsbone matrixbone modelingmicrobiomesystems biology - bone interactors

Identifiers

PMID39348436
PMCPMC11523134

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.