Evidence map›Paper›PMID 23547211›Full record

ArticleThe Journal of rheumatology2013

Cardiovascular events are not associated with MTHFR polymorphisms, but are associated with methotrexate use and traditional risk factors in US veterans with rheumatoid arthritis.

Lisa A Davis, Grant W Cannon, Lauren F Pointer, Leah M Haverhals, Roger K Wolff, Ted R Mikuls, Andreas M Reimold, Gail S Kerr, J Steuart Richards, Dannette S Johnson and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of rheumatology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 12% 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

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

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  14. Initiation of Disease-Modifying Therapies in Rheumatoid Arthritis Is Associated With Changes in Blood Pressure.Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases · 2018
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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

13 authors at 1 institution in 1 country.

Lisa A DavisDepartment of Rheumatology, University of Colorado School of Medicine, Denver, CO, USA. lisa.davis@ucdenver.edu
Grant W Cannon
Lauren F Pointer
Leah M Haverhals
Roger K Wolff
Ted R Mikuls
Andreas M Reimold
Gail S Kerr
J Steuart Richards
Dannette S Johnson
Robert Valuck
Allan Prochazka
Liron Caplan
University of Colorado Denver · US

Funding

Research Training in Rheumatology INCLUDE Down Syndrome SupplementT32AR007534 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI Kristine A. Kuhn · 1986 to 2026
$6.1M
NIAMS NIH HHS T32 AR007534NIAMS NIH HHS T32 AR007534-24
6 · The paper itself

Abstract

objectiveC677T and A1298C polymorphisms in the enzyme methylenetetrahydrofolate reductase (MTHFR) have been associated with increased cardiovascular (CV) events in non-rheumatoid arthritis (RA) populations. We investigated potential associations of MTHFR polymorphisms and use of methotrexate (MTX) with time-to-CV event in data from the Veterans Affairs Rheumatoid Arthritis (VARA) registry.

methodsVARA participants were genotyped for MTHFR polymorphisms. Variables included demographic information, baseline comorbidities, RA duration, autoantibody status, and disease activity. Patients' comorbidities and outcome variables were defined using International Classification of Diseases-9 and Current Procedural Terminology codes. The combined CV event outcome included myocardial infarction (MI), percutaneous coronary intervention, coronary artery bypass graft surgery, and stroke. Cox proportional hazards regression was used to model the time-to-CV event.

resultsData were available for 1047 subjects. Post-enrollment CV events occurred in 97 patients (9.26%). Although there was a trend toward reduced risk of CV events, MTHFR polymorphisms were not significantly associated with time-to-CV event. Time-to-CV event was associated with prior stroke (HR 2.01, 95% CI 1.03-3.90), prior MI (HR 1.70, 95% CI 1.06-2.71), hyperlipidemia (HR 1.57, 95% CI 1.01-2.43), and increased modified Charlson-Deyo index (HR 1.23, 95% CI 1.13-1.34). MTX use (HR 0.66, 95% CI 0.44-0.99) and increasing education (HR 0.87, 95% CI 0.80-0.95) were associated with a lower risk for CV events.

conclusionAlthough MTHFR polymorphisms were previously associated with CV events in non-RA populations, we found only a trend toward decreased association with CV events in RA. Traditional risk factors conferred substantial CV risk, while MTX use and increasing years of education were protective.

Indexed as

AdultAgedAged, 80 and overAntirheumatic AgentsArthritis, RheumatoidCardiovascular DiseasesFemaleGenotypeHumansMaleMethotrexateMethylenetetrahydrofolate Reductase (NADPH2)Middle AgedPolymorphism, Single NucleotideRegistriesRisk FactorsAntirheumatic AgentsMethotrexateMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanCARDIOVASCULAR DISEASESMETHOTREXATEMETHYLENETETRAHYDROFOLATE REDUCTASERHEUMATOID ARTHRITISSINGLE-NUCLEOTIDE POLYMORPHISM

Identifiers

PMID23547211
PMCPMC4097095
OpenAlexW2110870445

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.