Evidence map›Paper›PMID 23813577›Full record

ArticleRheumatology (Oxford, England)2013

Comorbidities are associated with poorer outcomes in community patients with rheumatoid arthritis.

Veena K Ranganath, Paul Maranian, David A Elashoff, Thasia Woodworth, Dinesh Khanna, Theodore Hahn, Catherine Sarkisian, Joel M Kremer, Daniel E Furst, Harold E Paulus

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
–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

51 citing papers in PubMed.

  1. Trial
  2. The burden of multimorbidity in patients with systemic lupus erythematosus - single-centre analysis.Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia · 2026
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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.

Veena K RanganathUniversity of California at Los Angeles, 1000 Veteran Avenue, Rehab Building 32-59, Los Angeles, CA 90095, USA. vranganath@mednet.ucla.edu.
Paul Maranian
David A Elashoff
Thasia Woodworth
Dinesh Khanna
Theodore Hahn
Catherine Sarkisian
Joel M Kremer
Daniel E Furst
Harold E Paulus

Funding

UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
Health Values and Minimally Important Differences in Systemic SclerosisK23AR053858 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KHANNA, DINESH · 2007 to 2011
$617k
Biomarkers for Early Therapeutic Response in Older RA PatientsK23AR057818 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RANGANATH, VEENA K · 2010 to 2014
$607k
NCATS NIH HHS UL1 TR000124NIAMS NIH HHS K23 AR053858NIAMS NIH HHS K23 AR053858-04NIAMS NIH HHS K23 AR057818NIAMS NIH HHS K23 AR057818-02
6 · The paper itself

Abstract

objectiveTo evaluate the impact of comorbidities on achieving remission by examining changes in the clinical disease activity index (CDAI) in RA patients in the community-based Consortium of Rheumatology Researchers of North America (CORRONA) registry.

methodsA subcohort of 1548 RA subjects with varying disease duration met the following inclusion criteria: started a DMARD/biologic agent, continued therapy ≥ 3 months, CDAI ≥ 2.8 at study entry and followed longitudinally from baseline to follow-up (mean time 7.46 months). Patients reported comorbidities according to a standardized list of 33 conditions. Entry characteristics were compared across age categories using one-way analysis of variance. Linear and logistic regression models were constructed to assess characteristics [e.g. age, disease duration, number of previous DMARDs/biologics, baseline modified health assessment questionnaire (MHAQ), baseline CDAI and number of comorbidities] associated with primary outcomes: change in CDAI (baseline to follow-up) and CDAI remission (yes/no).

resultsAlthough disease activity measures at entry were similar across age categories, older patients had more comorbidities, less improvement in CDAI/MHAQ and were less likely to attain remission at follow-up. However, after adjusting covariates an increasing number of patient-reported comorbidities and higher baseline CDAI (but not age) were consistently and independently associated with a lower likelihood of clinical improvement or remission (P < 0.001).

conclusionIn this observational cohort of community RA patients an increasing number of patients reported comorbidities, independently correlated with less CDAI improvement over time. These results reaffirm that comorbidities may be an important factor in consideration of treat-to-target recommendations and aid in understanding achievable RA therapeutic goals.

Indexed as

AdultAgedAged, 80 and overAge FactorsAntirheumatic AgentsArthritis, RheumatoidBiological ProductsComorbidityFemaleFollow-Up StudiesHumansMaleMiddle AgedRemission InductionSeverity of Illness IndexTreatment OutcomeAntirheumatic AgentsBiological Productsagecomorbiditiesremissionrheumatoid arthritis

Identifiers

PMID23813577
PMCPMC3775293

What OpenQuestion holds

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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.