Evidence map›Paper›PMID 40016267›Full record

ArticleNature communications2025

Circulating miR-126-3p is a mechanistic biomarker for knee osteoarthritis.

Thomas G Wilson, Madhu Baghel, Navdeep Kaur, Indrani Datta, Ian Loveless, Pratibha Potla, Devin Mendez, Logan Hansen, Kevin Baker, T Sean Lynch and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

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

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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

13 authors.

Thomas G WilsonBone and Joint Center, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI, USA.ORCID http://orcid.org/0000-0003-3416-5498
Madhu BaghelBone and Joint Center, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI, USA.
Navdeep KaurBone and Joint Center, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI, USA.ORCID http://orcid.org/0000-0003-0927-2910
Indrani DattaCenter for Bioinformatics, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI, USA.
Ian LovelessCenter for Bioinformatics, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI, USA.ORCID http://orcid.org/0000-0003-4645-6559
Pratibha PotlaSchroeder Arthritis Institute, University Health Network, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-3000-6820
Devin MendezBone and Joint Center, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI, USA.
Logan HansenDepartment of Orthopedic Surgery, Henry Ford Health, Detroit, MI, USA.ORCID http://orcid.org/0000-0003-0231-3628
Kevin BakerBone and Joint Center, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI, USA.
T Sean LynchDepartment of Orthopedic Surgery, Henry Ford Health, Detroit, MI, USA.
Vasilios MoutzourosDepartment of Orthopedic Surgery, Henry Ford Health, Detroit, MI, USA.
Jason DavisDepartment of Orthopedic Surgery, Henry Ford Health, Detroit, MI, USA.ORCID http://orcid.org/0000-0003-1615-0735
Shabana Amanda AliBone and Joint Center, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI, USA. sali14@hfhs.org.ORCID http://orcid.org/0000-0002-4339-9467

Funding

Arthritis National Research Foundation (ANRF) 953971
6 · The paper itself

Abstract

Osteoarthritis is a major contributor to pain and disability worldwide, yet there are currently no validated soluble biomarkers or disease-modifying treatments. Given that microRNAs are promising mechanistic biomarkers that can be therapeutically targeted, in this study, we aimed to identify and prioritize reproducible circulating microRNAs associated with radiographic knee osteoarthritis. Across four independent cohorts, we find circulating miR-126-3p is elevated in knee osteoarthritis versus controls. Across six primary human knee osteoarthritis tissues, miR-126-3p is highest in subchondral bone, fat pad and synovium, and lowest in cartilage. Following both intravenous and intra-articular miR-126-3p mimic treatment in a surgical mouse model of knee osteoarthritis, we show reduced disease severity in males. In human knee osteoarthritis biospecimens, miR-126-3p mimic treatment reduces genes and markers associated with angiogenesis, as well as genes linked to osteogenesis, adipogenesis, and synovitis-processes secondary to angiogenesis. Our findings indicate that miR-126-3p is elevated in knee osteoarthritis and mitigates disease severity, supporting its potential as a biomarker and therapeutic target.

Indexed as

MicroRNAsOsteoarthritis, KneeAgedAnimalsBiomarkersDisease Models, AnimalFemaleHumansMaleMiceMice, Inbred C57BLMiddle AgedBiomarkersMicroRNAsMIRN126 microRNA, human

Identifiers

PMID40016267
PMCPMC11868599

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.