Evidence map›Paper›PMID 40782426›Full record

ArticleSeminars in arthritis and rheumatism2025

Real-world persistence of urate-lowering therapy following a treat-to-target intervention: A two-year follow-up analysis of the STOP gout trial.

Samantha Kohn, Harlan Sayles, Lindsay N Helget, Bryant R England, Punyasha Roul, Jeff A Newcomb, Bridget Kramer, Anne Davis-Karim, Mary T Brophy, Ryan Ferguson and 6 more

Abstract read
In one paragraph

Article in Seminars in arthritis and rheumatism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

16 authors.

Samantha KohnVeterans Affairs (VA) Nebraska-Western Iowa Health Care System, Omaha, NE, United States; University of Nebraska Medical Center (UNMC), Omaha, NE United States.
Harlan SaylesDepartment of Biostatistics, UNMC, United States.
Lindsay N HelgetVeterans Affairs (VA) Nebraska-Western Iowa Health Care System, Omaha, NE, United States; University of Nebraska Medical Center (UNMC), Omaha, NE United States.
Bryant R EnglandVeterans Affairs (VA) Nebraska-Western Iowa Health Care System, Omaha, NE, United States; University of Nebraska Medical Center (UNMC), Omaha, NE United States.
Punyasha RoulUniversity of Nebraska Medical Center (UNMC), Omaha, NE United States.
Jeff A NewcombVeterans Affairs (VA) Nebraska-Western Iowa Health Care System, Omaha, NE, United States; University of Nebraska Medical Center (UNMC), Omaha, NE United States.
Bridget KramerVeterans Affairs (VA) Nebraska-Western Iowa Health Care System, Omaha, NE, United States; University of Nebraska Medical Center (UNMC), Omaha, NE United States.
Anne Davis-KarimVA Cooperative Studies Program Clinical Research Pharmacy Coordinating Center, Albuquerque, NM, United States.
Mary T BrophyVA Boston Cooperative Studies Program Coordinating Center, Boston, MA, United States; Boston University School of Medicine, VA Boston Health Care System, Boston, MA, United States.
Ryan FergusonVA Boston Cooperative Studies Program Coordinating Center, Boston, MA, United States.
Michael H PillingerVA New York Harbor Health Care System, New York, NY, United States; NYU Grossman School of Medicine, New York, NY, United States.
Tuhina NeogiBoston University School of Medicine, Boston, MA, United States.
Paul M PalevskyVA Pittsburgh Health Care System, Pittsburgh, PA United States; University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.
Hongsheng WuVA Boston Cooperative Studies Program Coordinating Center, Boston, MA, United States; Wentworth Institute of Technology, Boston, MA, United States.
James R O'DellVeterans Affairs (VA) Nebraska-Western Iowa Health Care System, Omaha, NE, United States; University of Nebraska Medical Center (UNMC), Omaha, NE United States.
Ted R MikulsVeterans Affairs (VA) Nebraska-Western Iowa Health Care System, Omaha, NE, United States; University of Nebraska Medical Center (UNMC), Omaha, NE United States. Electronic address: tmikuls@unmc.edu.

Funding

Project-005UL1TR001445 · NCATS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BREDELLA, MIRIAM ANTOINETTE, HOCHMAN, JUDITH S · 2015 to 2025
$103.5M
Tracking and Evaluation CoreU54GM115458 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI PHILIBERT, INGRID · 2016 to 2025
$42.8M
Research and Evaluation Support Core Unit (RESCU Core)P30AR072571 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI TUHINA NEOGI · 2019 to 2026
$6.9M
The Role of Urate in Knee Osteoarthritis-Related Inflammation, Pathology and PainK24AR070892 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI TUHINA NEOGI · 2017 to 2026
$1.1M
BLRD VA I01 BX003635CSRD VA I01 CX002358CSRD VA IK2 CX002203NCATS NIH HHS UL1 TR001445NIAMS NIH HHS K24 AR070892NIAMS NIH HHS P30 AR072571NIGMS NIH HHS U54 GM115458
6 · The paper itself

Abstract

objectiveThough gout guidelines endorse treat-to-target urate-lowering therapy (ULT), its long-term durability following treat-to-target implementation has not been extensively studied. Examining follow-up data from a trial implementing treat-to-target management, we evaluated the frequency and determinants of ULT persistence.

methodsThis analysis examined participants completing the 72-week STOP Gout trial with available follow-up data extending 2-years post-study. Participants were followed passively using administrative and electronic health record data with persistence defined by a ULT dispensing episode overlapping with the 2-year post-study time point. Associations of participant factors with ULT persistence were examined using multivariable logistic regression.

resultsParticipants in this analysis (n = 638) were predominantly male (99 %) and had a mean age of 62.7 years. At 2-years post-study, 66 % continued ULT. Adjusting for covariates, ≥2 rheumatology visits post-study (vs. none) was associated with greater ULT persistence (aOR 1.75; 95 % CI 1.13-2.72). ULT persistence was lower in individuals reporting Black/African American race (aOR 0.56; 95 % CI 0.36-0.87), Hispanic ethnicity (aOR 0.21; 95 % CI 0.09-0.50), and better quality-of-life at the beginning of post-study follow-up. Though not reaching significance, achievement of serum urate goal at 48-weeks during STOP Gout study demonstrated a borderline association with greater long-term persistence (aOR 1.68; 95 % CI 0.99-2.85).

conclusionThough interventions implementing treat-to-target ULT have demonstrated efficacy in trials, this study suggests that such interventions may have limited durability following transitions back to real-world gout management. The issue of limited treatment durability appears to be compounded among underrepresented patient populations and improved in the context of ongoing rheumatological care.

Indexed as

GoutGout SuppressantsUric AcidAgedAllopurinolFemaleFollow-Up StudiesHumansMaleMiddle AgedAllopurinolGout SuppressantsUric AcidDeterminants of healthGoutReal-world careTreatment persistenceTreat-to-targetUrate-lowering therapy

Identifiers

PMID40782426
PMCPMC13671858

What OpenQuestion holds

Textmetadata
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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.