Evidence map›Paper›PMID 32653044›Full record

Observational studyArthritis research & therapy2020

Initiating guideline-concordant gout treatment improves arterial endothelial function and reduces intercritical inflammation: a prospective observational study.

Michael Toprover, Binita Shah, Cheongeun Oh, Talia F Igel, Aaron Garza Romero, Virginia C Pike, Fatmira Curovic, Daisy Bang, Deana Lazaro, Svetlana Krasnokutsky and 2 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Arthritis research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

12 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

12 authors at 2 institutions in 1 country.

Michael ToproverSection of Rheumatology, VA New York Harbor Health Care System, New York, NY, USA.
Binita ShahSection of Cardiology, VA New York Harbor Health Care System, New York, NY, USA.
Cheongeun OhDivision of Biostatistics, Department of Population Health, NYU Grossman School of Medicine, New York, NY, USA.
Talia F IgelSection of Rheumatology, VA New York Harbor Health Care System, New York, NY, USA.
Aaron Garza RomeroSection of Rheumatology, VA New York Harbor Health Care System, New York, NY, USA.
Virginia C PikeSection of Rheumatology, VA New York Harbor Health Care System, New York, NY, USA.
Fatmira CurovicSection of Cardiology, VA New York Harbor Health Care System, New York, NY, USA.
Daisy BangSection of Rheumatology, VA New York Harbor Health Care System, New York, NY, USA.
Deana LazaroSection of Rheumatology, VA New York Harbor Health Care System, New York, NY, USA.
Svetlana KrasnokutskySection of Rheumatology, VA New York Harbor Health Care System, New York, NY, USA.
Stuart D KatzDivision of Cardiology, Department of Medicine, NYU Grossman School of Medicine, New York, NY, USA.
Michael H PillingerSection of Rheumatology, VA New York Harbor Health Care System, New York, NY, USA. michael.toprover@nyulangone.org.ORCID 0000-0003-3168-1542
VA NY Harbor Healthcare System · USNew York University · US

Funding

Project-005UL1TR001445 · NCATS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BREDELLA, MIRIAM ANTOINETTE, HOCHMAN, JUDITH S · 2015 to 2025
$103.5M
Studies on the effects of colchicine on neutrophil biology in acute myocardial infarctionR01HL146206 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SHAH, BINITA · 2019 to 2022
$2.4M
Biomedical Laboratory Research and Development, VA Office of Research and Development 1K2CS001074NCATS NIH HHS 1UL1TR001445NCATS NIH HHS UL1 TR001445NHLBI NIH HHS R01 HL146206NHLBI NIH HHS R01HL146206
6 · The paper itself

Abstract

backgroundPatients with gout have arterial dysfunction and systemic inflammation, even during intercritical episodes, which may be markers of future adverse cardiovascular outcomes. We conducted a prospective observational study to assess whether initiating guideline-concordant gout therapy with colchicine and a urate-lowering xanthine oxidase inhibitor (XOI) improves arterial function and reduces inflammation.

methodsThirty-eight untreated gout patients meeting American College of Rheumatology (ACR)/European League Against Rheumatism classification criteria for gout and ACR guidelines for initiating urate-lowering therapy (ULT) received colchicine (0.6 mg twice daily, or once daily for tolerance) and an XOI (allopurinol or febuxostat) titrated to ACR guideline-defined serum urate (sU) target. Treatment was begun during intercritical periods. The initiation of colchicine and XOI was staggered to permit assessment of a potential independent effect of colchicine. Brachial artery flow-mediated dilation (FMD) and nitrate-mediated dilation (NMD) assessed endothelium-dependent and endothelium-independent (smooth muscle) arterial responsiveness, respectively. High-sensitivity C-reactive protein (hsCRP), IL-1β, IL-6, myeloperoxidase (MPO) concentrations, and erythrocyte sedimentation rate (ESR) assessed systemic inflammation.

resultsFour weeks after achieving target sU concentration on colchicine plus an XOI, FMD was significantly improved (58% increase, p = 0.03). hsCRP, ESR, IL-1β, and IL-6 also all significantly improved (30%, 27%, 19.5%, and 18.8% decrease respectively; all p ≤ 0.03). Prior to addition of XOI, treatment with colchicine alone resulted in smaller numerical improvements in FMD, hsCRP, and ESR (20.7%, 8.9%, 13% reductions, respectively; all non-significant), but not IL-1β or IL-6. MPO and NMD did not change with therapy. We observed a moderate inverse correlation between hsCRP concentration and FMD responsiveness (R = - 0.41, p = 0.01). Subgroup analyses demonstrated improvement in FMD after achieving target sU concentration in patients without but not with established cardiovascular risk factors and comorbidities, particularly hypertension and hyperlipidemia.

conclusionsInitiating guideline-concordant gout treatment reduces intercritical systemic inflammation and improves endothelial-dependent arterial function, particularly in patients without established cardiovascular comorbidities.

Indexed as

GoutHyperuricemiaAllopurinolFebuxostatGout SuppressantsHumansInflammationAllopurinolFebuxostatGout SuppressantsAllopurinolColchicineC-reactive proteinFlow-mediated dilationGoutHyperuricemiaInflammationSubclinical cardiovascular diseaseUrate-lowering therapyXanthine oxidase inhibitor

Identifiers

PMID32653044
PMCPMC7353742
OpenAlexW3041161188

What OpenQuestion holds

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LicenceCC BY
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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.