Evidence map›Paper›PMID 39853943›Full record

ArticleACR open rheumatology2025

Ketogenic Diet-Associated Worsening of Osteoarthritis Histologic Secerity, Increased Pain Sensitivity and Gut Microbiome Dysbiosis in Mice.

Gabby Dyson, Montana Barrett, Leoni Schlupp, Emmaline Prinz, Nicholas Hannebut, Aleksander Szymczak, Cindy Miranda Brawner, Matlock A Jeffries

Abstract read
In one paragraph

Article in ACR open rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. The Interplay between the Gut and Ketogenic Diets in Health and Disease.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    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

8 authors.

Gabby DysonOklahoma Medical Research Foundation, Arthritis & Clinical Immunology Program and the Oklahoma City Veterans Affairs Medical Center.ORCID https://orcid.org/0009-0009-9617-696X
Montana BarrettOklahoma Medical Research Foundation, Arthritis & Clinical Immunology Program and the Oklahoma City Veterans Affairs Medical Center.ORCID https://orcid.org/0009-0006-1005-1401
Leoni SchluppOklahoma Medical Research Foundation, Arthritis & Clinical Immunology Program, Oklahoma City.ORCID https://orcid.org/0000-0002-2837-5942
Emmaline PrinzOklahoma Medical Research Foundation, Arthritis & Clinical Immunology Program, Oklahoma City.ORCID https://orcid.org/0000-0001-8497-6171
Nicholas HannebutOklahoma Medical Research Foundation, Arthritis & Clinical Immunology Program and the Oklahoma City Veterans Affairs Medical Center.ORCID https://orcid.org/0009-0000-7812-866X
Aleksander SzymczakOklahoma Medical Research Foundation, Arthritis & Clinical Immunology Program, Oklahoma City.ORCID https://orcid.org/0000-0002-9028-8428
Cindy Miranda BrawnerOklahoma Medical Research Foundation, Arthritis & Clinical Immunology Program and the Oklahoma City Veterans Affairs Medical Center.
Matlock A JeffriesOklahoma Medical Research Foundation, Arthritis & Clinical Immunology Program, the University of Oklahoma Health Sciences Center, and the Oklahoma City Veterans Affairs Medical Center.ORCID https://orcid.org/0000-0001-9516-4312

Funding

Visualizing insulin actions on neuronal metabolism and function using fluorescent biosensorsP20GM125528 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI William Edmund Sonntag · 2019 to 2026
$17.8M
An integrative study of circulating leukocyte composition, epigenetic patterns, and functional consequences in knee osteoarthritis.K08AR070891 · NIAMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI JEFFRIES, MATLOCK · 2017 to 2021
$862k
Intraarticular microbial DNA as a novel mediator of osteoarthritisR61AR078075 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI JEFFRIES, MATLOCK · 2020 to 2021
$861k
Intraarticular microbial DNA as a novel mediator of osteoarthritisR33AR078075 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI JEFFRIES, MATLOCK · 2022 to 2022
$437k
The peripheral blood microbiome as a potential biomarker of knee osteoarthritisR21AR085344 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI JEFFRIES, MATLOCK · 2024 to 2024
$413k
BLRD VA I01 BX004882Congressionally Directed Medical Research Programs PR191652NIAMS NIH HHS K08 AR070891NIAMS NIH HHS K08AR070891NIAMS NIH HHS R21 AR085344NIAMS NIH HHS R33 AR078075NIAMS NIH HHS R33AR078075NIAMS NIH HHS R61 AR078075NIAMS NIH HHS R61AR078075NIGMS NIH HHS P20 GM125528NIGMS NIH HHS P20GM125528
6 · The paper itself

Abstract

objectivesDietary interventions are a potentially powerful treatment option for knee osteoarthritis (OA). The objective of this study was to evaluate a well-formulated ketogenic diet (KD) in the context of knee OA histology and pain using the destabilization of the medial meniscus (DMM) mouse model and correlate with gut microbiome and systemic cytokine levels.

methodsAdult male mice underwent unilateral DMM or sham surgery and were then fed eight weeks of KD or chow. At baseline and every two weeks, mechanical allodynia of the operated and contralateral knees was assessed via analgesiometry. Knee joints were collected for histology, gut microbiome analysis was performed on cecal material via 16S sequencing, and serum cytokines were analyzed via Bio-Plex assay.

resultsKD mice had worse histopathologic OA after DMM (mean ± SEM Osteoarthritis Research Society International score: KD-DMM: 4.0 ± 0.5 vs chow-DMM: 2.7 ± 0.08; P = 0.02). KD mice had increased mechanical allodynia postsurgery (P = 0.005 in mixed-effects model). The gut microbiome changed substantially with KD: 59 clades were altered by KD in DMM and 39 by KD in sham (36 were shared, 25 overlapped with previous murine OA studies). Several clades were correlated on an individual-mouse level with both histology and allodynia (eg, Lactobacillus histology P = 0.004, allodynia P = 1 × 10

conclusionKD started immediately after OA induction via DMM is associated with worsened histologic outcomes. KD also worsens mechanical allodynia after either DMM or sham surgery. KD induces significant gut microbiome dysbiosis in clades previously associated with murine OA.

Identifiers

PMID39853943
PMCPMC11760994

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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.