Evidence map›Paper›PMID 40802523›Full record

ArticleRheumatology (Oxford, England)2025

Anxiety symptoms and associated factors in the Scleroderma Patient-centered Intervention Network (SPIN) cohort: a cross-sectional study.

Sabrina Provencher, Marie-Eve Carrier, Gabrielle Virgili-Gervais, Meira Golberg, Richard S Henry, Linda Kwakkenbos, Catherine Fortuné, Amy Gietzen, Karen Gottesman, Geneviève Guillot and 13 more

Abstract readMulticenter Study
In one paragraph

Article in Rheumatology (Oxford, England), 2025. 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. 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

23 authors.

Sabrina ProvencherLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.
Marie-Eve CarrierLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.
Gabrielle Virgili-GervaisLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.
Meira GolbergLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.
Richard S HenryLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.
Linda KwakkenbosDepartment of Clinical Psychology, Behavioural Science Institute, Radboud University, Nijmegen, The Netherlands.
Catherine FortunéOttawa Scleroderma Support Group, Ottawa, ON, Canada.
Amy GietzenNational Scleroderma Foundation, Tri-State Chapter, Buffalo, NY, USA.
Karen GottesmanNational Scleroderma Foundation, Los Angeles, CA, USA.
Geneviève GuillotSclérodermie Québec, Longueuil, QC, Canada.
Amanda Lawrie-JonesScleroderma Australia and Scleroderma Victoria, Melbourne, Victoria, Australia.
Maureen SauvéScleroderma Society of Ontario and Scleroderma Canada, Hamilton, ON, Canada.
Susan J BartlettDepartment of Medicine, McGill University, Montreal, QC, Canada.ORCID 0000-0001-9755-2490
Laura K HummersDivision of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Vanessa MalcarneDepartment of Psychology, San Diego State University, San Diego, CA, USA.
Maureen D MayesDivision of Rheumatology, University of Texas McGovern School of Medicine, Houston, TX, USA.
Michelle RichardScleroderma Atlantic, Halifax, NS, Canada.
James StempelScleroderma Chicago, Chicago, IL, USA.
Robyn K WojeckAmgen Inc, Thousand Oaks, CA, USA.
Luc MouthonService de Médecine Interne, Centre de Référence Maladies Autoimmunes et Autoinflammatoires Systémiques Rares d'Ile de France, de l'Est et de l'Ouest, Hôpital Cochin, Paris, France.ORCID 0000-0002-9838-246X
Andrea BenedettiDepartment of Medicine, McGill University, Montreal, QC, Canada.ORCID 0000-0002-8314-9497
Brett D ThombsLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.
Scleroderma Patient-centered Intervention Network Investigators

Funding

Arthritis SocietyCIHRFonds de Recherche du Québec-SantéJewish General Hospital FoundationJewish General Hospital, Montreal, QuebecLady Davis Institute for Medical ResearchMaster's Research AwardMcGill UniversityScleroderma Association of BCScleroderma AtlanticScleroderma Canada; Sclérodermie QuébecScleroderma Foundation of CaliforniaScleroderma ManitobaScleroderma New South WalesScleroderma SASKScleroderma Society of OntarioScleroderma VictoriaThe Scleroderma Patient-centered Intervention NetworkTier 1 Canada Research Chair
6 · The paper itself

Abstract

objectiveWe (1) compared anxiety symptom levels in a multinational SSc cohort to a general population normative sample and (2) evaluated sociodemographic, lifestyle and SSc disease factors associated with symptoms.

methodsScleroderma Patient-centered Intervention Network Cohort participants completed the Patient-Reported Outcomes Measurement Information System (PROMIS) Version 2 4a Anxiety domain upon enrolment. PROMIS domain scores use T-scores (mean = 50, S.D. = 10) calibrated to a United States normative sample. We compared T-scores to the PROMIS United States normative sample and, in SSc, assessed associations of sociodemographic, lifestyle and physician-reported disease-related variables with multivariable linear regression.

resultsAmong 2463 participants with SSc, mean anxiety symptom T-score (52.6, S.D. = 10.0, 95% CI 52.2, 53.0) was ∼1/3 S.D. higher than the United States general population mean of 50 (S.D. = 10), though within normal limits. Higher T-scores were associated with younger age (1.07 T-score points per 10 years, 95% CI 0.74, 1.40), female sex (1.81, 95% CI 0.63, 3.00), non-married status (0.99, 95% CI 0.14, 1.84), race or ethnicity other than White (1.79, 95% CI 0.72, 2.85), living in Canada (1.70, 95% CI 0.61, 2.79), the United Kingdom (1.53, 95% CI 0.06, 2.99) or France (2.01, 95% CI 0.98, 3.03) (vs the United States), higher BMI (0.11, 95% CI 0.03, 0.17), less time since non-Raynaud's symptom onset (0.82 per 10 years, 95% CI 0.40, 1.30), gastrointestinal involvement (2.70, 95% CI 1.52, 3.88), moderate small joint contractures (1.24, 95% CI 0.10, 2.38), the absence of interstitial lung disease (0.93, 95% CI -1.79, -0.07) and Sjögren disease (1.67, 95% CI 0.17, 3.17). Interstitial lung disease was not statistically significant when accounting for an interaction with country. Anxiety was also associated with pruritus and pain intensity in a sensitivity analysis that included variables with possible bi-directional pathways with anxiety.

conclusionAnxiety symptoms were somewhat elevated among individuals with SSc and associated with multiple sociodemographic and disease factors.

Indexed as

AnxietyScleroderma, SystemicAdultAgedCohort StudiesCross-Sectional StudiesFemaleHumansLife StyleMaleMiddle AgedPatient-Centered CarePatient Reported Outcome MeasuresUnited StatesanxietyPROMIS-29sclerodermaSSc

Identifiers

PMID40802523
PMCPMC12671864

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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.