Evidence map›Paper›PMID 37202358›Full record

ArticleRheumatology (Oxford, England)2024

Association between knee magnetic resonance imaging markers and knee symptoms over 6-9 years in young adults.

Ambrish Singh, Alison Venn, Leigh Blizzard, Lyn March, Felix Eckstein, Graeme Jones, Wolfgang Wirth, Flavia Cicuttini, Changhai Ding, Benny Antony

Open access · hybridAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2024. 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
0.5field-weighted citation impact, top 39% 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.

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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

10 authors at 4 institutions in 4 countries.

Ambrish SinghMenzies Institute for Medical Research, University of Tasmania, Hobart, TS, Australia.ORCID 0000-0002-4618-7507
Alison VennMenzies Institute for Medical Research, University of Tasmania, Hobart, TS, Australia.
Leigh BlizzardMenzies Institute for Medical Research, University of Tasmania, Hobart, TS, Australia.
Lyn MarchInstitute of Bone and Joint Research, Kolling Institute of Medical Research, University of Sydney, Sydney, NSW, Australia.
Felix EcksteinChondrometrics GmbH, Ainring, Germany.
Graeme JonesMenzies Institute for Medical Research, University of Tasmania, Hobart, TS, Australia.ORCID 0000-0002-9814-0006
Wolfgang WirthChondrometrics GmbH, Ainring, Germany.
Flavia CicuttiniDepartment of Epidemiology and Preventive Medicine, Monash University, Melbourne, VIC, Australia.
Changhai DingMenzies Institute for Medical Research, University of Tasmania, Hobart, TS, Australia.ORCID 0000-0002-9479-730X
Benny AntonyMenzies Institute for Medical Research, University of Tasmania, Hobart, TS, Australia.
University of Tasmania · AUParacelsus Medical University · ATMonash University · AUThe University of Sydney · AU

Funding

International Graduate Research ScholarshipNational Health and Medical Research Council 211316National Health and Medical Research Council of AustraliaResearch Enhancement 2015University of Tasmania
6 · The paper itself

Abstract

objectivesTo describe associations between MRI markers with knee symptoms in young adults.

methodsKnee symptoms were assessed using the WOMAC scale during the Childhood Determinants of Adult Health Knee Cartilage study (CDAH-knee; 2008-2010) and at the 6- to 9-year follow-up (CDAH-3; 2014-2019). Knee MRI scans obtained at baseline were assessed for morphological markers (cartilage volume, cartilage thickness, subchondral bone area) and structural abnormalities [cartilage defects and bone marrow lesions (BMLs)]. Univariable and multivariable (age, sex, BMI adjusted) zero-inflated Poisson (ZIP) regression models were used for analysis.

resultsThe participants' mean age in CDAH-knee and CDAH-3 were 34.95 (s.d. 2.72) and 43.27 (s.d. 3.28) years, with 49% and 48% females, respectively. Cross-sectionally, there was a weak but significant negative association between medial femorotibial compartment (MFTC) [ratio of the mean (RoM) 0.99971084 (95% CI 0.9995525, 0.99986921), P < 0.001], lateral femorotibial compartment (LFTC) [RoM 0.99982602 (95% CI 0.99969915, 0.9999529), P = 0.007] and patellar cartilage volume [RoM 0.99981722 (95% CI 0.99965326, 0.9999811), P = 0.029] with knee symptoms. Similarly, there was a negative association between patellar cartilage volume [RoM 0.99975523 (95% CI 0.99961427, 0.99989621), P = 0.014], MFTC cartilage thickness [RoM 0.72090775 (95% CI 0.59481806, 0.87372596), P = 0.001] and knee symptoms assessed after 6-9 years. The total bone area was negatively associated with knee symptoms at baseline [RoM 0.9210485 (95% CI 0.8939677, 0.9489496), P < 0.001] and 6-9 years [RoM 0.9588811 (95% CI 0.9313379, 0.9872388), P = 0.005]. The cartilage defects and BMLs were associated with greater knee symptoms at baseline and 6-9 years.

conclusionBMLs and cartilage defects were positively associated with knee symptoms, whereas cartilage volume and thickness at MFTC and total bone area were weakly and negatively associated with knee symptoms. These results suggest that the quantitative and semiquantitative MRI markers can be explored as a marker of clinical progression of OA in young adults.

Indexed as

Bone DiseasesCartilage, ArticularCartilage DiseasesOsteoarthritis, KneeBone MarrowCartilageChildFemaleHumansKnee JointMagnetic Resonance ImagingMaleYoung AdultBMLcartilage defectMRI markersOAWOMAC

Identifiers

PMID37202358
PMCPMC10836990
OpenAlexW4377014290

What OpenQuestion holds

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LicenceCC BY-NC
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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.