Evidence map›Paper›PMID 40035233›Full record

ArticleACR open rheumatology2025

Changes in Long-Term Glucocorticoid Use Among Older Adults After New Diagnosis of Late-Onset Rheumatoid Arthritis.

Jiha Lee, Jonathan Martindale, Beth I Wallace, Namrata Singh, Una E Makris, Julie P W Bynum

Abstract read
In one paragraph

Article in ACR open rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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  5. Review
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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

6 authors.

Jiha LeeUniversity of Michigan, Ann Arbor.ORCID https://orcid.org/0000-0002-6402-6563
Jonathan MartindaleUniversity of Michigan, Ann Arbor.
Beth I WallaceUniversity of Michigan, Ann Arbor, and VA Ann Arbor Healthcare System, Ann Arbor, Virginia.
Namrata SinghUniversity of Washington, Seattle.
Una E MakrisUniversity of Texas Southwestern Medical Center and VA North Texas Health Care System, Dallas.ORCID https://orcid.org/0000-0003-4750-0777
Julie P W BynumUniversity of Michigan, Ann Arbor.

Funding

Improving shared decision-making around the use of disease modifying anti-rheumatic drugs in patients with rheumatoid arthritis and cancerK23AR079588 · NIAMS · UNIVERSITY OF WASHINGTON · PI Namrata Singh · 2022 to 2026
$821k
Understanding disease modifying antirheumatic drug use in older adults with late-onset rheumatoid arthritisK23AG082727 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JIHA LEE · 2023 to 2026
$778k
Evaluation of treatment patterns and prescription medication use among older adults with late-onset rheumatoid arthritisR03AG067975 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, JIHA · 2020 to 2021
$308k
CSRD VA IK2 CX002430NIAMS NIH HHS K23 AR079588NIAMS NIH HHS K23AR079588NIA NIH HHS K23 AG082727NIA NIH HHS K23AG082727NIA NIH HHS R03 AG067975NIA NIH HHS R03AG067975U.S. Department of Veterans Affairs IIR 20-256U.S. Department of Veterans Affairs IK2CX002430
6 · The paper itself

Abstract

backgroundWe evaluated changes in long-term glucocorticoid (GC) use and factors associated with persistent GC use in older adults with late-onset rheumatoid arthritis (LORA).

methodsUsing 20% Medicare data from 2008 to 2017, we identified adults ≥66 years with a new diagnosis of LORA, disease-modifying antirheumatic drug (DMARD) use or at least two rheumatologist visits, and at least 12 months of follow-up data. Older adults were categorized as DMARD-exposed or DMARD-unexposed based on treatment during the 12 months after LORA diagnosis (index date). For each quarter after the index date, long-term GC use was defined as having oral GC prescriptions for at least 30 days with a dose >5 mg/day prednisone equivalent. We compared long-term GC use between quarter (Q)1 and Q4 and performed stratified mixed-effects logistic regression for factors associated with persistent GC use, defined as long-term GC use in Q2 to Q4.

resultsThe cohort included 15,425 individuals with two-thirds (62.5%) being DMARD-exposed. Between Q1 and Q4, the proportion of older adults on long-term GC declined from 44.1 to 24.9% (∆19.2%) among the DMARD-exposed and from 25.8 to 17.9% (∆7.9%) among the DMARD-unexposed. One year after the index date, 13.5% of the DMARD-exposed and 9.8% of the DMARD-unexposed were persistent GC users. In stratified mixed-effects logistic models, persistent GC use was associated with low-income subsidy status among the DMARD-exposed and with greater comorbidity burden among DMARD-unexposed.

conclusionLong-term GC use declined more among DMARD-exposed than DMARD-unexposed patients. One in seven DMARD-exposed and one in ten DMARD-unexposed have persistent GC use which is associated with financial barriers and multimorbidity that may limit the use of steroid-sparing DMARDs.

Identifiers

PMID40035233
PMCPMC11877135

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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.