Evidence map›Paper›PMID 27039382›Full record

ArticleArthritis research & therapy2016

Association between biomarkers of tissue inflammation and progression of osteoarthritis: evidence from the Rotterdam study cohort.

Fatemeh Saberi Hosnijeh, Anne Sofie Siebuhr, Andre G Uitterlinden, Edwin H G Oei, Albert Hofman, Morten A Karsdal, Sita M Bierma-Zeinstra, Anne C Bay-Jensen, Joyce B J van Meurs

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 4 pooled it
12.0field-weighted citation impact, top 1% 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

66 citing papers in PubMed, 4 syntheses or guidelines pooled it, 123 citations in OpenAlex.

  1. Pooled it
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6 more citing papers are in PubMed but not listed here.

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 2 countries.

Fatemeh Saberi HosnijehDepartment of Internal Medicine, Erasmus University Medical Center, P.O. Box 2040, Rotterdam, 3000, CA, Netherlands.
Anne Sofie SiebuhrBiomarkers and Research, Nordic Bioscience, Herlev, Denmark.
Andre G UitterlindenDepartment of Internal Medicine, Erasmus University Medical Center, P.O. Box 2040, Rotterdam, 3000, CA, Netherlands.
Edwin H G OeiDepartment of Radiology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Albert HofmanDepartment of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Morten A KarsdalBiomarkers and Research, Nordic Bioscience, Herlev, Denmark.
Sita M Bierma-ZeinstraDepartment of General Practice, Erasmus University Medical Center, Rotterdam, Netherlands.
Anne C Bay-JensenBiomarkers and Research, Nordic Bioscience, Herlev, Denmark.
Joyce B J van MeursDepartment of Internal Medicine, Erasmus University Medical Center, P.O. Box 2040, Rotterdam, 3000, CA, Netherlands. j.vanmeurs@erasmusmc.nl.
Erasmus MC · NLNordic Bioscience (Denmark) · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe aimed to investigate the prognostic value of two biomarkers of tissue inflammation, matrix metalloproteinase-dependent degradation of C-reactive protein (CRPM) and connective tissue type I collagen turnover (C1M), on the incidence and progression of radiographic osteoarthritis (OA) in the Rotterdam Study, a prospective cohort. Moreover, the independent effect of these biomarkers with respect to the established biomarkers of OA progression, like urinary type II collagen degradation (uCTX-II) and serum cartilage oligomeric protein (COMP), was evaluated.

methodsSerum levels of C1M, CRPM, COMP and CRP of 1335 participants aged >55 years were measured in fasting serum using ELISA. The commercial ELISA detecting CTX-II was used in urine. Radiographs at baseline and 5-year follow-up were scored for OA stage by Kellgren-Lawrence grade. The associations between progression and incidence of OA and the baseline biomarkers were examined using logistic regression and generalized estimating equations adjusted for age, sex, BMI, and possible other confounders.

resultsThe uCTX-II, COMP, and CRP concentrations were associated with the incidence and progression of OA. Moreover, OA progression was positively associated with CRPM (OR = 1.3, p = 0.01) and CRP (OR = 1.3, p = 0.01) levels with similar effect size as uCTX-II (OR = 1.3, p = 0.01) and COMP (OR = 1.2, p = 0.02). CRPM had prognostic value for progression of OA independent from the uCTX-II and COMP.

conclusionsOur study confirmed the associations between uCTX-II and COMP concentrations and OA progression. Importantly, we showed for the first time that CRPM predicts the risk of OA progression independent of the established biomarkers uCTX-II and COMP.

Indexed as

AgedBiomarkersCartilage Oligomeric Matrix ProteinCohort StudiesCollagen Type IIC-Reactive ProteinDisease ProgressionEnzyme-Linked Immunosorbent AssayFemaleHumansInflammationMaleMiddle AgedOsteoarthritisPeptide FragmentsPrognosisBiomarkersCartilage Oligomeric Matrix ProteinCollagen Type IIC-Reactive ProteinC-terminal cross-linking telopeptide of type II collagen, humanPeptide FragmentsTSP5 protein, humanBiomarkerCRPInflammationOsteoarthritisProspective cohort

Identifiers

PMID27039382
PMCPMC4818486
OpenAlexW2313555702

What OpenQuestion holds

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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.