Evidence map›Paper›PMID 35309864›Full record

ReviewJBMR plus2022

Animal Models of Bone Marrow Lesions in Osteoarthritis.

Andrew Bowen, David Shamritsky, Josue Santana, Ian Porter, Erica Feldman, Sarah L Pownder, Matthew F Koff, Kei Hayashi, Christopher J Hernandez

Open access · goldAbstract readReview
In one paragraph

Review in JBMR plus, 2022. 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
0.7field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
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

9 authors at 2 institutions in 1 country.

Andrew BowenSibley School of Mechanical and Aerospace Engineering Cornell University Ithaca NY USA.
David ShamritskySibley School of Mechanical and Aerospace Engineering Cornell University Ithaca NY USA.
Josue SantanaSibley School of Mechanical and Aerospace Engineering Cornell University Ithaca NY USA.
Ian PorterCollege of Veterinary Medicine Cornell University Ithaca NY USA.
Erica FeldmanCollege of Veterinary Medicine Cornell University Ithaca NY USA.
Sarah L PownderHospital for Special Surgery New York NY USA.
Matthew F KoffHospital for Special Surgery New York NY USA.
Kei HayashiCollege of Veterinary Medicine Cornell University Ithaca NY USA.
Christopher J HernandezSibley School of Mechanical and Aerospace Engineering Cornell University Ithaca NY USA.ORCID https://orcid.org/0000-0002-0712-6533
Cornell University · USHospital for Special Surgery · US

Funding

The Role of Bone Resorption in Bone Marrow LesionsR21AR073454 · NIAMS · CORNELL UNIVERSITY · PI HERNANDEZ, CHRISTOPHER JOHN · 2018 to 2019
$407k
NIAMS NIH HHS R21 AR073454
6 · The paper itself

Abstract

Bone marrow lesions are abnormalities in magnetic resonance images that have been associated with joint pain and osteoarthritis in clinical studies. Increases in the volume of bone marrow lesions have been associated with progression of joint degeneration, leading to the suggestion that bone marrow lesions may be an early indicator of-or even a contributor to-cartilage loss preceding irreversible damage to the joint. Despite evidence that bone marrow lesions play a role in osteoarthritis pathology, very little is known about the natural history of bone marrow lesions and their contribution to joint degeneration. As a result, there are limited data regarding the cell activity within a bone marrow lesion and any associated bone-cartilage cross-talk. Animal models provide the best approach for understanding bone marrow lesions at their early, reversible stages. Here, we review the few animal studies of bone marrow lesions. An ideal animal model of a bone marrow lesion occurs in joints large enough to accurately measure bone marrow lesion volume. Additionally, the ideal animal model would facilitate the study of bone-cartilage cross-talk by generating the bone marrow lesion immediately adjacent to subchondral bone and would do so without causing direct damage to neighboring soft tissues to isolate the effects of the bone marrow lesion on cartilage loss. Early reports demonstrate the feasibility of such an animal model. Given the irreversible nature of osteoarthritic changes in the joint, factors such as bone marrow lesions that are present early in disease pathogenesis remain an enticing target for new therapeutic approaches. © 2022 The Authors.

Indexed as

BONEBONE MARROW LESIONJOINTMICRODAMAGEOSTEOARTHRITIS

Identifiers

PMID35309864
PMCPMC8914161
OpenAlexW4210695859

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.