Evidence map›Paper›PMID 31228216›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2019

Sexually Dimorphic Influence of Neonatal Antibiotics on Bone.

Matteo M Pusceddu, Patricia J Stokes, Alice Wong, Melanie G Gareau, Damian C Genetos

Open access · bronzeAbstract read
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.3field-weighted citation impact, top 44% of its field
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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Regional and Sexual Dimorphism in Murine Skeletal Responses to Osteocytic HIF Pathway Modulation.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2026
    Article
  3. Review
  4. Article
  5. Article
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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

5 authors at 1 institution in 1 country.

Matteo M PuscedduDepartment of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine, University of California, Davis, 1089 Veterinary Medicine Drive, Davis, California, 95616.
Patricia J StokesDepartment of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine, University of California, Davis, 1089 Veterinary Medicine Drive, Davis, California, 95616.
Alice WongDepartment of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine, University of California, Davis, 1089 Veterinary Medicine Drive, Davis, California, 95616.
Melanie G GareauDepartment of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine, University of California, Davis, 1089 Veterinary Medicine Drive, Davis, California, 95616.
Damian C GenetosDepartment of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine, University of California, Davis, 1089 Veterinary Medicine Drive, Davis, California, 95616.ORCID 0000-0002-8599-2867
University of California, Davis · US

Funding

Mouse Metabolic Phenotyping Center (MMPC) at UC DavisU2CDK092993 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LLOYD, KC KENT · 2016 to 2021
$5.9M
Mouse Metabolic Phenotyping Center (MMPC) at UC DavisU24DK092993 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LLOYD, KC KENT · 2011 to 2015
$4.1M
The microbiota-gut-brain axis in Alzheimers diseaseR01AT009365 · NCCIH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GAREAU, MELANIE G · 2017 to 2021
$2.2M
Integration of TGFb-ALK5 on Wnt signaling and mechanotransduction in boneR01AR064255 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GENETOS, DAMIAN C · 2013 to 2017
$1.7M
NCCIH NIH HHS R01 AT009365NCCIH NIH HHS R01AT009365NIAMS NIH HHS R01 AR064255NIAMS NIH HHS R01AR064255NIDDK NIH HHS U24 DK092993NIDDK NIH HHS U24DK092993NIDDK NIH HHS U2C DK092993
6 · The paper itself

Abstract

The gut microbiome (GM) contributes to host development, metabolism, and disease. Perturbations in GM composition, elicited through chronic administration of oral antibiotics (Abx) or studied using germ-free environments, alter bone mass, and microarchitecture. However, studies primarily involved chronic Abx exposure to adult mice prior to evaluating the skeletal phenotype. Children are more prone to infection with bacterial pathogens than adults and are thus treated more frequently with broad-spectrum Abx; consequently, Abx treatment disproportionately occurs during periods of greatest skeletal plasticity to anabolic cues. Because early-life exposures may exert long-lasting effects on adult health, we hypothesized that acute Abx administration during a developmentally sensitive period would elicit lasting effects on the skeletal phenotype. To test this hypothesis, neonatal mice were treated with Abx (P7-P23; oral gavage) or vehicle (water); GM composition, gut physiology, and bone structural and material properties were assessed in adulthood (8 weeks). We found sexually dimorphic effects of neonatal Abx administration on GM composition, gut barrier permeability, and the skeleton, indicating a negative role for neonatal Abx on bone mass and quality. © 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 37:2122-2129, 2019.

Indexed as

Sex CharacteristicsAmpicillinAnimalsAnimals, NewbornAnti-Bacterial AgentsBone and BonesColonFemaleGastrointestinal MicrobiomeMaleMiceMice, Inbred C57BLNeomycinPermeabilityPhenotypeVancomycinAmpicillinAnti-Bacterial AgentsNeomycinVancomycinantibioticsbonegut microbiotaintestinal barrier

Identifiers

PMID31228216
PMCPMC6886746
OpenAlexW2953304049

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.