Evidence map›Paper›PMID 33421361›Full record

ArticleArthritis care & research2022

Multivariable Modeling of Biomarker Data From the Phase I Foundation for the National Institutes of Health Osteoarthritis Biomarkers Consortium.

David J Hunter, Leticia A Deveza, Jamie E Collins, Elena Losina, Jeffrey N Katz, Michael C Nevitt, John A Lynch, Frank W Roemer, Ali Guermazi, Michael A Bowes and 5 more

Abstract read
In one paragraph

Article in Arthritis care & research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Article
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  4. Bone Shape Feature Differences in Single and Recurrent Patellar Dislocations via Statistical Shape Modeling.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2026
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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

15 authors.

David J HunterRoyal North Shore Hospital and University of Sydney, Sydney, Australia.ORCID 0000-0003-3197-752X
Leticia A DevezaRoyal North Shore Hospital and University of Sydney, Sydney, Australia.ORCID 0000-0002-2766-7142
Jamie E CollinsBrigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0001-8413-007X
Elena LosinaBrigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-3424-0892
Jeffrey N KatzBrigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Michael C NevittUniversity of California, San Francisco.
John A LynchUniversity of California, San Francisco.
Frank W RoemerBoston University School of Medicine, Boston, Massachusetts, and University of Erlangen, Nuremberg, Erlangen, Germany.ORCID 0000-0001-9238-7350
Ali GuermaziBoston University School of Medicine, Boston, Massachusetts.
Michael A BowesImorphics Ltd., Manchester, UK.
Erik B DamUniversity of Copenhagen and BiomedIQ, Copenhagen, Denmark.
Felix EcksteinParacelsus Medical University, Salzburg, Austria, and Chondrometrics GmbH, Ainring, Germany.ORCID 0000-0002-2014-8278
C Kent KwohUniversity of Arizona College of Medicine, Tucson.ORCID 0000-0001-5937-550X
Steve HoffmannFoundation for the National Institutes of Health, North Bethesda, Maryland.
Virginia B KrausDuke University School of Medicine, Durham, North Carolina.

Funding

Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI Virginia B Kraus · 2006 to 2026
$24.6M
VERITY: Value and Evidence in Rheumatology using bioInformaTics, and advanced analYticsP30AR072577 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Daniel Hal Solomon · 2017 to 2026
$9.8M
Treatment of Meniscal Problems in Osteoarthritis: TeMPOU01AR071658 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI KATZ, JEFFREY NEIL · 2017 to 2022
$4.1M
Clinical impact and cost-effectiveness of pain management in knee OAR01AR064320 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI LOSINA, ELENA · 2013 to 2017
$3.3M
Patient Oriented Research and Mentoring Program in OrthopedicsK24AR057827 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI LOSINA, ELENA · 2010 to 2019
$1.7M
Qualification of Prognostic and Diagnostic Biomarkers of Knee OsteoarthritisR01AR071450 · NIAMS · DUKE UNIVERSITY · PI KRAUS, VIRGINIA · 2017 to 2019
$1.7M
Pain sensitization in a trial of physical therapy for osteoarthritis and meniscal tearR21AR076156 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI KATZ, JEFFREY NEIL · 2019 to 2020
$616k
NEW PHARMACOLOGY ASPECTS RELATED TO CARBONIC ANHYDRASER01HL022258 · NHLBI · UNIVERSITY OF FLORIDA · PI MAREN, THOMAS H · 1985 to 1986
–
DATA COORDINATING CENTER FOR THE OSTEOARTHRITIS INITIATIVE-264022258N01AR022258 · NIAMS · UNIVERSITY OF CALIFORNIA SYS OFFICE/PRES · 2003 to 2003
–
NHLBI NIH HHS N01 AR022258NIAMS NIH HHS K24 AR057827NIAMS NIH HHS P30 AR072577NIAMS NIH HHS R01 AR064320NIAMS NIH HHS R01 AR071450NIAMS NIH HHS R21 AR076156NIAMS NIH HHS U01 AR071658NIA NIH HHS P30 AG028716NIH HHS N01-AR-22258NIH HHS N01-AR-22259NIH HHS N01-AR-22260NIH HHS N01-AR-22261NIH HHS N01-AR-22262the Pivotal Osteoarthritis Initiative (OAI) MRI Analyses (POMA) study HH-SN-2682010000
6 · The paper itself

Abstract

objectiveTo determine the optimal combination of imaging and biochemical biomarkers for use in the prediction of knee osteoarthritis (OA) progression.

methodsThe present study was a nested case-control trial from the Foundation of the National Institutes of Health OA Biomarkers Consortium that assessed study participants with a Kellgren/Lawrence grade of 1-3 who had complete biomarker data available (n = 539 to 550). Cases were participants' knees that had radiographic and pain progression between 24 and 48 months compared to baseline. Radiographic progression only was assessed in secondary analyses. Biomarkers (baseline and 24-month changes) that had a P value of <0.10 in univariate analysis were selected, including quantitative cartilage thickness and volume on magnetic resonance imaging (MRI), semiquantitative MRI markers, bone shape and area, quantitative meniscal volume, radiographic progression (trabecular bone texture [TBT]), and serum and/or urine biochemical markers. Multivariable logistic regression models were built using 3 different stepwise selection methods (complex models versus parsimonious models).

resultsAmong baseline biomarkers, the number of locations affected by osteophytes (semiquantitative), quantitative central medial femoral and central lateral femoral cartilage thickness, patellar bone shape, and semiquantitative Hoffa-synovitis predicted OA progression in most models (C statistic 0.641-0.671). In most models, 24-month changes in semiquantitative MRI markers (effusion-synovitis, meniscal morphologic changes, and cartilage damage), quantitative central medial femoral cartilage thickness, quantitative medial tibial cartilage volume, quantitative lateral patellofemoral bone area, horizontal TBT (intercept term), and urine N-telopeptide of type I collagen predicted OA progression (C statistic 0.680-0.724). A different combination of imaging and biochemical biomarkers (baseline and 24-month change) predicted radiographic progression only, which had a higher C statistic of 0.716-0.832.

conclusionThe present study highlights the combination of biomarkers with potential prognostic utility in OA disease-modifying trials. Properly qualified, these biomarkers could be used to enrich future trials with participants likely to experience progression of knee OA.

Indexed as

Cartilage, ArticularOsteoarthritis, KneeSynovitisBiomarkersDisease ProgressionHumansKnee JointMagnetic Resonance ImagingNational Institutes of Health (U.S.)United StatesBiomarkers

Identifiers

PMID33421361
PMCPMC8267050

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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.