Evidence map›Paper›PMID 28575534›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2017

CCL2 in the Circulation Predicts Long-Term Progression of Interstitial Lung Disease in Patients With Early Systemic Sclerosis: Data From Two Independent Cohorts.

Minghua Wu, Murray Baron, Claudia Pedroza, Gloria A Salazar, Jun Ying, Julio Charles, Sandeep K Agarwal, Marie Hudson, Janet Pope, Xiaodong Zhou and 4 more

Open access · greenAbstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 81 citations in OpenAlex.

  1. Trial
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  8. Associations with, and predictors of, progression in systemic sclerosis-related interstitial lung disease: a scoping literature review.European respiratory review : an official journal of the European Respiratory Society · 2026
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  10. Observational
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  18. Immune network · 2024
    Article
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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

14 authors at 6 institutions in 2 countries.

Minghua WuMcGovern Medical School, University of Texas Health Science Center at Houston.
Murray BaronMcGill University, Montreal, Quebec, Canada.
Claudia PedrozaMcGovern Medical School, University of Texas Health Science Center at Houston.
Gloria A SalazarMcGovern Medical School, University of Texas Health Science Center at Houston.ORCID 0000-0003-4286-2250
Jun YingMcGovern Medical School, University of Texas Health Science Center at Houston.
Julio CharlesMcGovern Medical School, University of Texas Health Science Center at Houston.
Sandeep K AgarwalBaylor College of Medicine, Houston, Texas.
Marie HudsonJewish General Hospital and Lady Davis Institute for Medical Research, Montreal, Quebec, Canada.
Janet PopeSt. Joseph's Health Care, University of Western Ontario, London, Ontario, Canada.
Xiaodong ZhouMcGovern Medical School, University of Texas Health Science Center at Houston.
John D ReveilleMcGovern Medical School, University of Texas Health Science Center at Houston.
Marvin J FritzlerUniversity of Calgary, Calgary, Alberta, Canada.
Maureen D MayesMcGovern Medical School, University of Texas Health Science Center at Houston.
Shervin AssassiMcGovern Medical School, University of Texas Health Science Center at Houston.
The University of Texas Health Science Center at Houston · USBaylor College of Medicine · USJewish General Hospital · CAMcGill University · CAUniversity of Calgary · CAWestern University · CA

Funding

U OF TEXAS HLTH SCI CTR HOUSTON CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCESUL1RR024148 · NCRR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2006 to 2010
$27.9M
Role of TGF-beta and CTGF Signaling Transgenic Mouse Models of SclerodermaP50AR054144 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI TAN, FILEMON K. · 2006 to 2010
$7.7M
Two-Stage Genome-Wide Association Study in Systemic SclerosisR01AR055258 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MAYES, MAUREEN MAUREEN · 2008 to 2012
$5.9M
Cadherin-11 Regulation Of Dermal Fribrosis And Macrophage FunctionR01AR062056 · NIAMS · BAYLOR COLLEGE OF MEDICINE · PI AGARWAL, SANDEEP K · 2012 to 2016
$1.7M
SCLERODERMA FAMILY REGISTRY AND DNA REPOSITORY-264002251-264002251-264002251N01AR002251 · NIAMS · WAYNE STATE UNIVERSITY · PI MAYES, MAUREEN · 2000 to 2006
$659k
Molecular Markers for Progression of Pulmonary Fibrosis in Systemic SclerosisK23AR061436 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ASSASSI, SHERVIN · 2011 to 2014
$494k
NCRR NIH HHS UL1 RR024148NIAMS NIH HHS K23 AR061436NIAMS NIH HHS N01 AR002251NIAMS NIH HHS P50 AR054144NIAMS NIH HHS R01 AR055258NIAMS NIH HHS R01 AR062056
6 · The paper itself

Abstract

objectiveThere are few clinical predictors of the progression of systemic sclerosis (SSc)-related interstitial lung disease (ILD). The purpose of this study was to examine the predictive significance of key cytokines for long-term progression of ILD and survival in 2 independent cohorts of patients with early SSc.

methodsPlasma levels of 11 Th1/Th2 cytokines (interleukin-1β [IL-1β], IL-5, IL-6, IL-8, IL-10, IL-12, IL-13, tumor necrosis factor, CCL2, interferon-inducible T cell α chemoattractant, and interferon-γ-inducible 10-kd protein) were measured in 266 patients with early SSc in the Genetics versus Environment in Scleroderma Outcome Study (GENISOS) discovery cohort. Levels of CCL2, IL-10, and IL-6 were measured in 171 patients with early SSc in the Canadian Scleroderma Research Group (CSRG) replication cohort. The primary outcome measure was a decline in the forced vital capacity percent predicted (FVC%) value over time. A joint analysis of longitudinal FVC% values and survival was performed.

resultsAfter adjustment for age, sex, and ethnicity, CCL2 and IL-10 were found to be significant predictors of ILD progression in the discovery cohort. Higher CCL2 levels predicted a faster decline in FVC% values (b = -0.57, P = 0.032), while higher IL-10 levels predicted a slower decline (b = 0.26, P = 0.01). A higher CCL2 value was also predictive of poorer survival (hazard ratio 1.76, P = 0.030). In the CSRG replication cohort, higher CCL2 levels predicted a faster decline in FVC% values (b = -0.58, P = 0.038), but neither IL-10 nor IL-6 had predictive significance. A higher CCL2 level also predicted poorer survival (hazard ratio 3.89, P = 0.037).

conclusionHigher CCL2 levels in the circulation were predictive of ILD progression and poorer survival in patients with early SSc, findings that support the notion that CCL2 has a role as a biomarker and potential therapeutic target.

Indexed as

AdultBiomarkersCanadaChemokine CCL2Cohort StudiesCytokinesDisease ProgressionFemaleHumansLongitudinal StudiesLung Diseases, InterstitialMalePredictive Value of TestsPrognosisProportional Hazards ModelsScleroderma, SystemicBiomarkersCCL2 protein, humanChemokine CCL2Cytokines

Identifiers

PMID28575534
PMCPMC5575955
OpenAlexW2621221129

What OpenQuestion holds

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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.