Evidence map›Paper›PMID 36585217›Full record

Trial reportRMD open2022

Baseline serum levels of cross-linked carboxy-terminal telopeptide of type I collagen predict abatacept treatment response in methotrexate-naive, anticitrullinated protein antibody-positive patients with early rheumatoid arthritis.

Chun Wu, Yanhua Hu, Peter Schafer, Sean E Connolly, Robert Wong, Signe Holm Nielsen, Anne-Christine Bay-Jensen, Paul Emery, Yoshiya Tanaka, Vivian P Bykerk and 4 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in RMD open, 2022. 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 32% 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, 3 citations in OpenAlex.

  1. Trial
  2. Article
  3. Observational
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 8 institutions in 5 countries.

Chun WuBristol Myers Squibb, Princeton, New Jersey, USA.
Yanhua HuBristol Myers Squibb, Princeton, New Jersey, USA.
Peter SchaferBristol Myers Squibb, Princeton, New Jersey, USA.
Sean E ConnollyBristol Myers Squibb, Princeton, New Jersey, USA.
Robert WongBristol Myers Squibb, Princeton, New Jersey, USA.
Signe Holm NielsenNordic Bioscience, Herlev, Denmark.
Anne-Christine Bay-JensenNordic Bioscience, Herlev, Denmark.
Paul EmeryUniversity of Leeds and Leeds NIHR Biomedical Research Centre, Leeds, UK.ORCID 0000-0002-7429-8482
Yoshiya TanakaUniversity of Occupational and Environmental Health, Kitakyushu, Japan.ORCID 0000-0002-0807-7139
Vivian P BykerkHospital for Special Surgery, New York, New York, USA.ORCID 0000-0002-1219-3845
Clifton O BinghamJohns Hopkins University, Baltimore, Maryland, USA.
Thomas Wj HuizingaLeiden University Medical Center, Leiden, Netherlands.ORCID 0000-0001-7033-7520
Roy FleischmannUniversity of Texas Southwestern Medical Center, Metroplex Clinical Research Center, Dallas, Texas, USA.ORCID 0000-0002-6630-1477
Jinqi LiuBristol Myers Squibb, Princeton, New Jersey, USA jinqi.liu@bms.com.ORCID 0000-0002-0094-9801
Bristol-Myers Squibb (United States) · USNordic Bioscience (Denmark) · DKHospital for Special Surgery · USJohns Hopkins University · USLeiden University Medical Center · NLMetroplex Clinical Research Center · USUniversity of Leeds · GBUniversity of Occupational and Environmental Health Japan · JP

Funding

Molecular Pathways in Treatment Response and Flare in RAUH2AR067691 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI BYKERK, VIVIAN P, IVASHKIV, LIONEL B · 2014 to 2020
$2.0M
NIAMS NIH HHS UH2 AR067691
6 · The paper itself

Abstract

objectiveTo investigate correlations between biomarkers of bone remodelling and extracellular matrix turnover with baseline disease activity and treatment response in patients with early rheumatoid arthritis (RA).

methods

resultsPatient characteristics were similar between overall (n=752) and biomarker subgroup (n=535) populations and across treatments. At baseline, neoepitopes of matrix metalloproteinase-mediated degradation products of types III and IV collagen and of C reactive protein (CRP) showed the greatest correlations with disease activity; cross-linked carboxy-terminal telopeptide of type I collagen (CTX-I) showed weak correlation. Only CTX-I predicted treatment response; baseline CTX-I levels were significantly associated with achieving Simplified Disease Activity Index remission and Disease Activity Score in 28 joints (DAS28 (CRP)) <2.6 (weeks 24 and 52), and American College of Rheumatology 70 response (week 52), in patients treated with abatacept+MTX but not abatacept placebo+MTX. CTX-I predicted significant differential response between arms for DAS28 (CRP) <2.6 (week 24). Treatment differences were greater for abatacept+MTX in patients with medium/high versus low baseline CTX-I.

conclusionIn MTX-naive, ACPA-positive patients with early RA, baseline CTX-I predicted treatment response to abatacept+MTX but not abatacept placebo+MTX.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidAbataceptAnti-Citrullinated Protein AntibodiesBiomarkersCollagen Type IC-Reactive ProteinDrug Therapy, CombinationHumansMethotrexateTreatment OutcomeAbataceptAnti-Citrullinated Protein AntibodiesAntirheumatic AgentsBiomarkersCollagen Type IC-Reactive ProteinMethotrexateAbataceptAnti-Citrullinated Protein AntibodiesArthritis, RheumatoidMethotrexate

Identifiers

PMID36585217
PMCPMC9809248
OpenAlexW4313365103

What OpenQuestion holds

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LicenceCC BY-NC
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.