Evidence map›Paper›PMID 29723633›Full record

ArticleOsteoarthritis and cartilage2018

Associations between the chemokine biomarker CCL2 and knee osteoarthritis outcomes: the Johnston County Osteoarthritis Project.

L Longobardi, J M Jordan, X A Shi, J B Renner, T A Schwartz, A E Nelson, D A Barrow, V B Kraus, A Spagnoli

Abstract read
In one paragraph

Article in Osteoarthritis and cartilage, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
–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

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  13. Chemokine (C-C Motif) Ligand 2/Chemokine Receptor 2 (CCR2) Axis Blockade to Delay Chondrocyte Hypertrophy as a Therapeutic Strategy for Osteoarthritis.Medical science monitor : international medical journal of experimental and clinical research · 2021
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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

9 authors.

L LongobardiDivision of Rheumatology, Allergy and Immunology and the Thurston Arthritis Research Center, University of North Carolina-Chapel Hill, NC, USA. Electronic address: lara_longobardi@med.unc.edu.
J M JordanDivision of Rheumatology, Allergy and Immunology and the Thurston Arthritis Research Center, University of North Carolina-Chapel Hill, NC, USA. Electronic address: joanne_jordan@med.unc.edu.
X A ShiDivision of Rheumatology, Allergy and Immunology and the Thurston Arthritis Research Center, University of North Carolina-Chapel Hill, NC, USA. Electronic address: xyshi@email.unc.edu.
J B RennerDepartment of Radiology, University of North Carolina-Chapel Hill, NC, USA. Electronic address: jordan_renner@med.unc.edu.
T A SchwartzDivision of Rheumatology, Allergy and Immunology and the Thurston Arthritis Research Center, University of North Carolina-Chapel Hill, NC, USA; Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina-Chapel Hill, NC, USA. Electronic address: tschwart@email.unc.edu.
A E NelsonDivision of Rheumatology, Allergy and Immunology and the Thurston Arthritis Research Center, University of North Carolina-Chapel Hill, NC, USA. Electronic address: amanda_nelson@med.unc.edu.
D A BarrowSchool of Dentistry, University of North Carolina-Chapel Hill, NC, USA. Electronic address: David_Barrow@unc.edu.
V B KrausDuke Molecular Physiology Institute and Division of Rheumatology, Department of Medicine, Duke University School of Medicine, Durham, NC, USA. Electronic address: vbk@duke.edu.
A SpagnoliDepartment of Pediatrics, Rush University Medical Center, Chicago, IL, USA. Electronic address: Anna_Spagnoli@rush.edu.

Funding

Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI Sarah B. Peskoe · 2006 to 2026
$24.6M
Project 3P60AR049465 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JORDAN, JOANNE M. · 2003 to 2008
$6.0M
Johnston County Osteoarthritis Project: Arthritis, Disability, and Other Chronic DiseasesU01DP006266 · DP · UNIV OF NORTH CAROLINA CHAPEL HILL · PI NELSON, AMANDA E · 2016 to 2020
$3.8M
Role of CCR2 in osteoarthritisR01AR070821 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Lara Longobardi · 2017 to 2026
$3.1M
Women's knee motion patterns in functional activitiesP60AR030701 · NIAMS · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI WINFIELD, JOHN B · 1986 to 2001
$1.9M
Molecular Mechanisms in Joint DevelopmentR01AR057042 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SPAGNOLI, ANNA · 2010 to 2014
$1.6M
NCCDPHP CDC HHS U01 DP006266NIAMS NIH HHS P60 AR030701NIAMS NIH HHS P60 AR049465NIAMS NIH HHS R01 AR057042NIAMS NIH HHS R01 AR070821NIA NIH HHS P30 AG028716
6 · The paper itself

Abstract

objectiveOur study analyzes the association between chemokine-ligand-2 (CCL2) serum concentrations at baseline and knee radiographic osteoarthritis (OA) (knee-rOA), knee-rOA progression, individual radiographic features and knee symptomatic OA at 5-year follow-up.

designOA outcomes were analyzed in a community-based cohort including a baseline enrollment and a 5-year follow-up. Baseline CCL2 serum concentrations were assessed by multiplex assay and associated with presence or progression of individual radiographic features at 5-year follow-up. Separate multiple logistic regression models were used to examine adjusted associations between baseline CCL2 and each of the knee OA variables at follow-up. CCL2 at baseline was modeled as an explanatory variable, whereas each of the knee OA variables at follow-up served as the response variables. Models were adjusted for age, BMI, race, and sex. Trend tests were conducted to assess any linear effect on outcomes across CCL2 tertiles.

resultsParticipants (n = 168) had a median age of 57-years and median BMI of 29 kg/m2. About 63% of all participants were women, and 58% Caucasian (42% African American). In adjusted logistic models, continuous log-CCL2 was significantly associated with knee-rOA. For each unit increase in log CCL2, the odds of having knee-rOA at follow-up was increased by 72%. CCL2 tertiles showed significant linear associations with presence and progression of knee-rOA and medial joint space narrowing (JSN), but not with presence or progression of osteophytes, bone sclerosis, knee symptoms, or symptomatic knee-rOA.

conclusionsSerum CCL2 may help to elucidate some mechanisms of joint destruction and identify individuals with higher odds of structural knee changes.

Indexed as

Disease ProgressionAgedBiomarkersChemokine CCL2Cohort StudiesFemaleHumansLogistic ModelsMaleMiddle AgedMultivariate AnalysisOsteoarthritis, KneePrognosisRadiographySensitivity and SpecificitySeverity of Illness IndexBiomarkersChemokine CCL2BiomarkersChemokinesOsteoarthritis

Identifiers

PMID29723633
PMCPMC6098742

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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.