Evidence map›Paper›PMID 26882094›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2016

Changes in Body Mass Related to the Initiation of Disease-Modifying Therapies in Rheumatoid Arthritis.

Joshua F Baker, Brian C Sauer, Grant W Cannon, Chia-Chen Teng, Kaleb Michaud, Said Ibrahim, Erik Jorgenson, Lisa Davis, Liron Caplan, Amy Cannella and 1 more

Open access · greenAbstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
4.8field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 citations in OpenAlex.

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  10. The Effect of TNF-Cardiology research and practice · 2022
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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

11 authors at 7 institutions in 1 country.

Joshua F BakerPhiladelphia VA Medical Center and University of Pennsylvania, Philadelphia.
Brian C SauerSalt Lake City VA Medical Center and University of Utah, Salt Lake City.
Grant W CannonSalt Lake City VA Medical Center and University of Utah, Salt Lake City.
Chia-Chen TengSalt Lake City VA Medical Center and University of Utah, Salt Lake City.
Kaleb MichaudUniversity of Nebraska Medical Center, Omaha, and National Data Bank for Rheumatic Diseases, Wichita, Kansas.
Said IbrahimCenter for Health Equity Research and Promotion, Philadelphia VA Medical Center, and University of Pennsylvania, Philadelphia.
Erik JorgensonPhiladelphia VA Medical Center and University of Pennsylvania, Philadelphia.
Lisa DavisDenver VA Medical Center, Denver, Colorado.
Liron CaplanDenver VA Medical Center, Denver, Colorado.
Amy CannellaUniversity of Nebraska Medical Center, Omaha, VA Nebraska-Western Iowa Health Care System, Omaha, Nebraska.
Ted R MikulsUniversity of Nebraska Medical Center, Omaha, VA Nebraska-Western Iowa Health Care System, Omaha, Nebraska.
Denver VA Medical Center · USPhiladelphia VA Medical Center · USUniversity of Nebraska Medical Center · USUniversity of Utah · USLake City VA Medical Center · USUniversity of Pennsylvania · USVA Nebraska Western Iowa Health Care System · US

Funding

Racial Disparity in the Utilization of Joint Replacement for OsteoarthritisK24AR055259 · NIAMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI IBRAHIM, SAID A · 2007 to 2019
$1.2M
Body composition, bone structure, and joint damage in rheumatoid arthritisIK2CX000955 · VA · PHILADELPHIA VA MEDICAL CENTER · PI BAKER, JOSHUA F. · 2013 to 2017
–
CSRD VA IK2 CX000955Intramural VA VA999999NIAMS NIH HHS K24 AR055259
6 · The paper itself

Abstract

objectiveUnintentional weight loss is important and can be predictive of long-term outcomes in patients with rheumatoid arthritis (RA). This study was undertaken to assess how primary therapies for RA may influence changes in body mass index (BMI) in RA patients from a large administrative database.

methodsUnique dispensing episodes of methotrexate, prednisone, leflunomide, and tumor necrosis factor inhibitors (TNFi) administered to RA patients were identified from the US Department of Veterans Affairs pharmacy databases. Values for C-reactive protein (CRP) level and BMI closest to the time point within 30 days of the treatment course start date and at follow-up time points were linked. Missing laboratory values were imputed. Weight loss was defined as a decrease in BMI of >1 kg/m(2) . Regression models were used to evaluate changes in BMI during each drug treatment as compared to treatment with methotrexate. To assess the impact of confounding by indication, propensity scores for use of each drug were incorporated in analyses using matched-weighting techniques.

resultsIn total, 52,662 treatment courses in 32,859 RA patients were identified. At 6 months from the date of prescription fill, weight gain was seen among patients taking methotrexate, those taking prednisone, and those taking TNFi. On average, compared to methotrexate-treated patients, prednisone-treated patients had significantly more weight gain, while leflunomide-treated patients demonstrated weight loss. In multivariable models, more weight loss (β = -0.41 kg/m(2) , 95% confidence interval [95% CI] -0.46, -0.36; P < 0.001) and a greater risk of weight loss (odds ratio 1.73, 95% CI 1.55, 1.79; P < 0.001) were evident among those receiving leflunomide compared to those receiving methotrexate. Treatment with prednisone was associated with greater weight gain (β = 0.072 kg/m(2) , 95% CI 0.042, 0.10; P < 0.001). These associations persisted in analyses adjusted for propensity scores and in sensitivity analyses.

conclusionLeflunomide is associated with significantly more, but modest, weight loss, while prednisone is associated with greater weight gain compared to other therapies for RA.

Indexed as

Body Mass IndexAnti-Inflammatory AgentsAntirheumatic AgentsArthritis, RheumatoidBody WeightFemaleHumansIsoxazolesLeflunomideMaleMethotrexateMiddle AgedPrednisoneTumor Necrosis Factor-alphaAnti-Inflammatory AgentsAntirheumatic AgentsIsoxazolesLeflunomideMethotrexatePrednisoneTumor Necrosis Factor-alpha

Identifiers

PMID26882094
PMCPMC4963297
OpenAlexW2278670734

What OpenQuestion holds

Textmetadata
LicenceTDM
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.