Evidence map›Paper›PMID 40702741›Full record

ArticleArthritis care & research2026

Evaluating the Longitudinal Association of Rheumatoid Arthritis Disease Activity With Phenotypic Frailty: Evidence for Secondary Frailty?

Hannah F Brubeck, Kylie E Riggles, Riley S Bass, Elizabeth R Wahl, George Mount, Dolores M Shoback, James S Andrews, Jose M Garcia, Ariela R Orkaby, Joshua F Baker and 3 more

Abstract read
In one paragraph

Article in Arthritis care & research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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.

Hannah F BrubeckVA Puget Sound Health Care System, Seattle, Washington.ORCID 0009-0007-1964-5318
Kylie E RigglesVA Puget Sound Health Care System, Seattle, Washington.
Riley S BassVA Puget Sound Health Care System, Seattle, Washington.
Elizabeth R WahlVA Puget Sound Health Care System and University of Washington, Seattle, Washington.
George MountVA Puget Sound Health Care System and University of Washington, Seattle, Washington.
Dolores M ShobackSan Francisco VA Medical Center and University of California San Francisco, San Francisco, California.
James S AndrewsUniversity of Alabama at Birmingham, Birmingham VA Health Care System, and Atlanta-Birmingham VA Geriatric Research Education and Clinical Center, Birmingham, Alabama.
Jose M GarciaVA Puget Sound Health Care System, Puget Sound Geriatric Research Education and Clinical Center, and University of Washington, Seattle, Washington.
Ariela R OrkabyNew England Geriatric Research, Education, and Clinical Center, VA Boston Healthcare System, Brigham and Women's Hospital, and Harvard Medical School, Boston, Massachusetts.
Joshua F BakerCorporal Crescenz VA Medical Center and University of Pennsylvania, Philadelphia, Pennsylvania.
Patricia P KatzUniversity of California San Francisco, San Francisco, California.ORCID 0000-0002-8146-2519
Katherine D WyshamVA Puget Sound Health Care System, Puget Sound Geriatric Research Education and Clinical Center, and University of Washington, Seattle, Washington.
Courtney N LoeckerUniversity of Nebraska Medical Center and Omaha VA Medical Center, Omaha, Nebraska.ORCID 0000-0002-2754-5233

Funding

Improving cancer-related fatigue, sexual dysfunction and quality of life in older men with cancer and androgen deficiencyR01AG061558 · NIA · SEATTLE INST FOR BIOMEDICAL/CLINICAL RES · PI BASARIA, SHEHZAD, DEL FABBRO, EGIDIO · 2019 to 2025
$3.4M
Improving Patient-Important Outcomes with Testosterone Replacement in Hypogonadal Men with a Prior History of CancerR01CA239208 · NCI · SEATTLE INST FOR BIOMEDICAL/CLINICAL RES · PI BASARIA, SHEHZAD, GARCIA, JOSE M. · 2019 to 2025
$3.3M
SArcopenia in Men with Prostate Cancer undergoing ADT (SAP-ADT)R01CA279220 · NCI · SEATTLE INST FOR BIOMEDICAL/CLINICAL RES · PI Jose M. Garcia, Sina A Gharib · 2024 to 2026
$1.4M
BLRD VA I01 BX002807CSRD VA IK2 CX002351NCI NIH HHS R01 CA239208NCI NIH HHS R01 CA279220NIA NIH HHS R01 AG061558RRD VA I01 RX003644RRD VA I01 RX004770
6 · The paper itself

Abstract

objectiveThe cross-sectional association between rheumatoid arthritis (RA) disease activity and frailty has been described; however, the longitudinal relationship is less well understood. We evaluated the association between disease activity and frailty over time.

methodsWe used a longitudinal RA cohort established at the Department of Veterans Affairs Puget Sound Health Care System. RA disease activity (Disease Activity Score in 28 joints using the C-reactive protein level [DAS28-CRP]) and frailty (measured by the Fried Frailty Phenotype [FFP]) were evaluated at baseline and at one year. Frailty was categorized as robust, prefrail, or frail. Ordinal logistic regressions assessed the cross-sectional associations of DAS28-CRP and frailty at baseline and at one year. Paired t-tests and multivariable mixed ordinal logistic regressions assessed the longitudinal associations of DAS28-CRP and frailty. Models were adjusted for age, sex, disease duration, prednisone use, conventional synthetic disease-modifying antirheumatic drug (DMARD) use, and biologic DMARD use.

resultsA total of 132 patients with RA aged 64.2 ± 11.3 years were included; 73% were male, 69% were White, 11% were Black, and 12% reported multiple races. The mean ± SD baseline DAS28-CRP was 3.9 ± 1.3, and frailty was categorized as robust in 35 (27%) patients, prefrail in 77 (58%) patients, and frail in 20 (15%) patients. DAS28-CRP (per 1-unit increase) was associated with a higher FFP category at baseline (adjusted odds ratio [aOR] 1.98, P < 0.0001). Disease activity increased in those whose frailty score worsened at one year (mean ± SD change score 0.61 ± 0.96, P = 0.0121). An increased DAS28-CRP was independently associated with a higher frailty category over one year (aOR 3.31, P < 0.0001; n = 65).

conclusionDisease activity is independently associated with phenotypic frailty. Increased disease activity over time is associated with worsening frailty status. Future studies are needed to explore this longitudinal relationship and to determine if controlling disease activity can mitigate frailty.

Indexed as

Arthritis, RheumatoidFrailtyAgedAntirheumatic AgentsC-Reactive ProteinCross-Sectional StudiesFemaleHumansLongitudinal StudiesMaleMiddle AgedPhenotypeSeverity of Illness IndexAntirheumatic AgentsC-Reactive Protein

Identifiers

PMID40702741
PMCPMC12747155

What OpenQuestion holds

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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.