Evidence map›Paper›PMID 29266428›Full record

ReviewJournal of orthopaedic research : official publication of the Orthopaedic Research Society2018

Bone marrow lesions in osteoarthritis: What lies beneath.

Tamara Alliston, Christopher J Hernandez, David M Findlay, David T Felson, Oran D Kennedy

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% 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

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

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  19. High-ResolutionAnalytical chemistry · 2023
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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 5 institutions in 3 countries.

Tamara AllistonDepartment of Orthopaedic Surgery, University of California San Francisco, California.
Christopher J HernandezSibley School of Mechanical and Aerospace Engineering, Meinig School of Biomedical Engineering, Cornell University, Hospital for Special Surgery, Ithaca, New York.
David M FindlayDiscipline of Orthopaedics and Trauma, The University of Adelaide, Adelaide, South Australia, 5005, Australia.
David T FelsonClinical Epidemiology Research and Training Unit Boston University School of Medicine, Boston, Massachusetts.
Oran D KennedyDepartment of Anatomy and Tissue Engineering Research Group, Royal College of Surgeons in Ireland, 123 St Stephens Green, Dublin 2, Dublin, Ireland.
Boston University · USHospital for Special Surgery · USRoyal College of Surgeons in Ireland · IEUniversity of Adelaide · AUUniversity of California, San Francisco · US

Funding

The mechanistic control of bone quality and joint crosstalk by osteocytesR01DE019284 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HERNANDEZ, CHRISTOPHER JOHN · 2009 to 2024
$7.6M
Skeletal Biology and Biomechanics (SBB) CoreP30AR075055 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI EDWARD C HSIAO · 2019 to 2026
$7.1M
The Role of Bone Resorption in Bone Marrow LesionsR21AR073454 · NIAMS · CORNELL UNIVERSITY · PI HERNANDEZ, CHRISTOPHER JOHN · 2018 to 2019
$407k
AAOS/ORS Tackling Joint Disease by Understanding Crosstalk between Cartilage and Bone Research SymposiumR13AR068913 · NIAMS · AMERICAN ACADEMY OF ORTHOPAEDIC SURGEONS · PI ALLISTON, TAMARA N · 2015 to 2015
$15k
NIAMS NIH HHS P30 AR075055NIAMS NIH HHS R13 AR068913NIAMS NIH HHS R21 AR073454NIDCR NIH HHS R01 DE019284
6 · The paper itself

Abstract

Osteoarthritis (OA) is the most common joint disease in the United States, affecting more than 30 million people, and is characterized by cartilage degeneration in articulating joints. OA can be viewed as a group of overlapping disorders, which result in functional joint failure. However, the precise cellular and molecular events within which lead to these clinically observable changes are neither well understood nor easily measurable. It is now clear that multiple factors, in multiple joint tissues, contribute to degeneration. Changes in subchondral bone are recognized as a hallmark of OA, but are normally associated with late-stage disease when degeneration is well established. However, early changes such as Bone Marrow Lesions (BMLs) in OA are a relatively recent discovery. BMLs are patterns from magnetic resonance images (MRI) that have been linked with pain and cartilage degeneration. Their potential utility in predicting progression, or as a target for therapy, is not yet fully understood. Here, we will review the current state-of-the-art in this field under three broad headings: (i) BMLs in symptomatic OA: malalignment, joint pain, and disease progression; (ii) biological considerations for bone-cartilage crosstalk in joint disease; and (iii) mechanical factors that may underlie BMLs and drive their communication with other joint tissues. Thus, this review will provide insights on this topic from a clinical, biological, and mechanical perspective. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 36:1818-1825, 2018.

Indexed as

AnimalsBone DiseasesBone MarrowCartilage, ArticularCartilage DiseasesDisease ProgressionHumansKnee JointMagnetic Resonance ImagingOsteoarthritisOsteoarthritis, KneePainTransforming Growth Factor betaTransforming Growth Factor betabone-cartilage crosstalkmicrodamagePainsubchondralTGF-β

Identifiers

PMID29266428
PMCPMC8607515
OpenAlexW2778795974

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.