Evidence map›Paper›PMID 41419188›Full record

ArticleJoint bone spine2026

High disease activity is associated with incident osteoporotic fractures among veterans with rheumatoid arthritis.

Katherine D Wysham, Hannah F Brubeck, Aaron Baraff, Punyasha Roul, Marianna Olave, John S Richards, Paul Monach, Dolores M Shoback, Patricia P Katz, Brian C Sauer and 6 more

Abstract readMulticenter Study
In one paragraph

Article in Joint bone spine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Katherine D WyshamVA Puget Sound Health Care System, Seattle, WA, United States; University of Washington, Seattle, WA, United States; Puget Sound Geriatrics Research Education and Clinical Center, Seattle, WA, United States. Electronic address: katherine.wysham@va.gov.
Hannah F BrubeckVA Puget Sound Health Care System, Seattle, WA, United States.
Aaron BaraffVA Puget Sound Health Care System, Seattle, WA, United States.
Punyasha RoulUniversity of Nebraska Medical Center, Omaha, NE, United States.
Marianna OlaveCorporal Crescenz VA Medical Center, Philadelphia, PA, United States.
John S RichardsVA Pittsburgh Healthcare System, Pittsburgh, PA, United States; University of Pittsburg, Pittsburgh, PA, United States.
Paul MonachVA Boston Healthcare System, Boston, MA, United States; Brigham and Women's Hospital, Boston, MA, United States.
Dolores M ShobackSan Francisco VA Medical Center, San Francisco, CA, United States; University of California San Francisco, San Francisco, CA, United States.
Patricia P KatzUniversity of California San Francisco, San Francisco, CA, United States.
Brian C SauerVA Salt Lake City, Salt Lake City, UT, United States; University of Utah, Salt Lake City, UT, United States.
Beth WallaceVA Ann Arbor Health Care System, Ann Arbor, MI, United States; University of Michigan, Ann Arbor, MI, United States.
Jose M GarciaVA Puget Sound Health Care System, Seattle, WA, United States; University of Washington, Seattle, WA, United States; Puget Sound Geriatrics Research Education and Clinical Center, Seattle, WA, United States.
Grant W CannonVA Salt Lake City, Salt Lake City, UT, United States; University of Utah, Salt Lake City, UT, United States.
Ted R MikulsVA Nebraska-Western Iowa Health Care System, Omaha, NE, United States; University of Nebraska Medical Center, Omaha, NE, United States.
Bryant R EnglandVA Nebraska-Western Iowa Health Care System, Omaha, NE, United States; University of Nebraska Medical Center, Omaha, NE, United States.
Joshua F BakerCorporal Crescenz VA Medical Center, Philadelphia, PA, United States; University of Pennsylvania, Philadelphia, PA, United States.

Funding

Tracking and Evaluation CoreU54GM115458 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ESTABROOKS, PAUL · 2016 to 2025
$42.8M
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 BX002807BLRD VA I01 BX003635CSRD VA IK2 CX002203CSRD VA IK2 CX002351CSRD VA IK2 CX002430NCI NIH HHS R01 CA239208NCI NIH HHS R01 CA279220NIA NIH HHS R01 AG061558NIGMS NIH HHS U54 GM115458RRD VA I01 RX003644RRD VA I01 RX004770
6 · The paper itself

Abstract

objectivesRheumatoid arthritis (RA) increases osteoporosis and fracture risk. The relationship between disease activity and fracture is not well characterized. We aimed to study whether RA disease activity and its components were associated with incident osteoporotic fracture.

methodsData were from the multicenter Veterans Affairs RA (VARA) registry. Fractures were identified by ICD9/10 codes and validated by chart review. Multivariable Cox regression was used to quantify associations of time-varying and cumulative RA disease activity, using DAS28-ESR, with incident osteoporotic fracture. To directly compare hazard ratios (HRs), DAS28-ESR components were scaled, centered and evaluated in multivariable models. Sensitivity analyses, including evaluating DAS28-ESR categories, were also performed.

resultsAmong 2912 veterans, 248 (9%) experienced incident osteoporotic fracture. Those who fractured were more likely to be female (19 versus 11%), White (83 vs. 75%) and had higher baseline disease activity (DAS28-ESR 4.0±1.5 vs. 3.8±1.6). The time-varying model demonstrated an 18% increased risk of incident osteoporotic fracture per unit increase of DAS28-ESR (aHR 1.18 [95% CI 1.09-1.28], P<0.001). The cumulative model revealed a 3% increased risk per DAS28-ESR unit-year (aHR 1.03 [95% CI 1.01-1.05], P<0.001). Patient global assessment of disease activity had the highest point estimates of the disease activity components in both time-varying and cumulative models. Compared to remission, moderate and high disease activity carried a 2-fold risk of incident osteoporotic fracture (aHR 2.24 and 2.01 respectively, both P<0.01).

conclusionTime-varying and cumulative RA disease activity are associated with incident osteoporotic fracture. These data support achieving low disease activity or remission to reduce the risk of incident osteoporotic fracture.

Indexed as

Arthritis, RheumatoidOsteoporotic FracturesVeteransAgedFemaleHumansIncidenceMaleMiddle AgedProportional Hazards ModelsRegistriesRetrospective StudiesRisk AssessmentRisk FactorsSeverity of Illness IndexUnited StatesDisease activityFracturesOsteoporosisRheumatoid arthritis

Identifiers

PMID41419188
PMCPMC12747156

What Socratic 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 Socratic graph.