Evidence map›Paper›PMID 30418120›Full record

ArticleClinical and experimental rheumatology

Body mass index and persistence of conventional DMARDs and TNF inhibitors in rheumatoid arthritis.

Caroline B McCulley, Jennifer L Barton, Grant W Cannon, Brian C Sauer, Chia Chen Teng, Michael D George, Liron Caplan, Bryant R England, Ted R Mikuls, Joshua F Baker

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Clinical and experimental rheumatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02694185 (Secondary Event Prevention Using Population Risk Management After PCI), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 11% 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.

NCT02694185 nacompletednot on this map

Secondary Event Prevention Using Population Risk Management After PCI

TypeinterventionalSponsorVA Office of Research and DevelopmentRan2016 to 2025Enrolled5,269ConditionsMyocardial Ischemia, Rheumatic DiseasesArmsCaplan IVR
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 21 citations in OpenAlex.

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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 at 1 institution in 1 country.

Caroline B McCulleyVA Portland Health Care System; Oregon Health & Science University, OR, USA. caroline.bonafede@gmail.com.
Jennifer L BartonVA Portland Health Care System; Oregon Health & Science University, OR, USA.
Grant W CannonVA Salt Lake City Healthcare System; University of Utah; Salt Lake City VA Medical Center (IDEAS 2.0) University of Utah, Division of Epidemiology, Team VERITAS, OR, USA.
Brian C SauerVA Salt Lake City Healthcare System; University of Utah; Salt Lake City VA Medical Center (IDEAS 2.0) University of Utah, Division of Epidemiology, Team VERITAS, OR, USA.
Chia Chen TengVA Salt Lake City Healthcare System; University of Utah; Salt Lake City VA Medical Center (IDEAS 2.0) University of Utah, Division of Epidemiology, Team VERITAS, OR, USA.
Michael D GeorgeDivision of Rheumatology, University of Pennsylvania, Philadelphia, PA, USA.
Liron CaplanDepartment of Medicine, Rocky Mountain VA Medical Center, Aurora, CO, USA.
Bryant R EnglandVA Nebraska-Western Iowa Health Care Center and the University of Nebraska Medical Center, Omaha, NE, USA.
Ted R MikulsVA Nebraska-Western Iowa Health Care Center and the University of Nebraska Medical Center, Omaha, NE, USA.
Joshua F BakerDivision of Rheumatology, University of Pennsylvania, Philadelphia, and Corporal Michael C. Crescenz VA Medical Center, Philadelphia, PA, USA.
University of Pennsylvania · US

Funding

Tracking and Evaluation CoreU54GM115458 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HOLSTEIN, SARAH A · 2016 to 2025
$42.8M
UNMC Summer Undergraduate Alcohol Research ProgramR25AA020818 · NIAAA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Kristina L Bailey · 2012 to 2026
$931k
Goal concordance in rheumatoid arthritis in diverse populationsK23AR064372 · NIAMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI BARTON, JENNIFER L · 2015 to 2019
$805k
CSRD VA I01 CX000896CSRD VA IK2 CX000955NIAAA NIH HHS R25 AA020818NIAMS NIH HHS K23 AR064372NIGMS NIH HHS U54 GM115458
6 · The paper itself

Abstract

objectivesObese patients with rheumatoid arthritis (RA) may be more likely to discontinue therapy than non-obese patients, possibly signifying a more refractory phenotype. The purpose of this study was to examine the association between body mass index (BMI) and discontinuation rates for different RA treatments accounting for confounding factors.

methodsVeterans Affairs administrative databases were used to define initial courses of methotrexate (MTX), hydroxychloroquine, sulfasalazine, prednisone, and self-injectable tumour necrosis factor inhibitors (TNFi). Discontinuation was defined as a lapse in drug refill >90 days. Using overweight BMI (25-30 kg/m2) as the referent group, multivariable Cox proportional hazards models were used to evaluate associations between BMI category and time to treatment discontinuation.

resultsThere were 46,970 initial RA treatment courses identified from 2005-2014 among 23,669 Veterans with RA. In multivariable models, severe obesity (BMI >35 kg/m2), compared to overweight BMI, was not associated with treatment discontinuation with the exception of prednisone [HR 1.10 (1.04, 1.17) p<0.001]. Patients with low (<20 kg/m2) and normal BMI (20-25 kg/m2) were more likely to discontinue MTX, TNFi, and HCQ compared to overweight patients. Other factors associated with earlier MTX and/or TNFi discontinuation included female sex, black race, greater comorbidity, depression, malignancy, congestive heart failure, current smoking, and more recent calendar year.

conclusionsObesity was not associated with therapy discontinuation among veterans with RA after accounting for confounding factors, suggesting that obesity is not a biological mediator of more refractory disease. Conversely, low BMI, comorbidity, and depression were identified as important predictors of drug discontinuation.

Indexed as

Arthritis, RheumatoidBody Mass IndexAntirheumatic AgentsDrug UtilizationFemaleHumansMethotrexatePredictive Value of TestsRisk AssessmentRisk FactorsTreatment OutcomeTumor Necrosis Factor-alphaAntirheumatic AgentsMethotrexateTumor Necrosis Factor-alpha

Identifiers

PMID30418120
PMCPMC7836911
OpenAlexW2969499634

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.