Safoora Fatima,Janet E Pope,Lillian-Ruiheng Chen,Orit Schieir,Marie-France Valois,Susan J Bartlett,Gilles Boire,Glen Hazlewood,Carol Hitchon,Diane Tin,Carter Thorne,Bindee Kuriya,Hugues Allard-Chamard,Vivian P Bykerk,Louis Bessette,
{"title":"Higher comorbidities associated with less improvement in disease activity in early rheumatoid arthritis: results from CATCH cohort.","authors":"Safoora Fatima,Janet E Pope,Lillian-Ruiheng Chen,Orit Schieir,Marie-France Valois,Susan J Bartlett,Gilles Boire,Glen Hazlewood,Carol Hitchon,Diane Tin,Carter Thorne,Bindee Kuriya,Hugues Allard-Chamard,Vivian P Bykerk,Louis Bessette,","doi":"10.1093/rheumatology/keaf350","DOIUrl":null,"url":null,"abstract":"OBJECTIVES\r\nComorbidities negatively influence remission rates in rheumatoid arthritis (RA). This study estimated the effects of comorbidities on components of disease activity in early RA (ERA).\r\n\r\nMETHODS\r\nUsing the Rheumatic Disease Comorbidity Index (RDCI), the influence of comorbidities on trajectories of components of the SDAI (Simple Disease Activity Index) was assessed in participants with ERA enrolled in Canadian Early Arthritis Cohort (CATCH) over the first year of treatment. Adjusted effects of RDCI scores categorized 0, 1, 2, and ≥ 3 on SDAI trajectories over time were analyzed using multivariable generalized estimating equations (GEE) models adjusted for multiple confounders.\r\n\r\nRESULTS\r\nERA participants (N = 2248) had a mean (SD) symptom duration of 5.7 (3) months; mean age 55 (15) years and 72% were female. Baseline SDAI was 29 (15), with 90% having moderate-high SDAI. Baseline RDCI scores were 0 in 888 (40%), 1 in 547 (24%), 2 in 451 (20%), and ≥3 in 362 (16%). While baseline disease activity was similar across comorbidity groups, patients with higher RDCI scores showed worse SDAI trajectories over the first year of RA treatment. Higher RDCI scores were independently associated with pain, patient and physician global assessments over time.\r\n\r\nCONCLUSION\r\nThis large real-world analysis of ERA patients seen in routine rheumatology practice across Canada showed that while RA disease activity across comorbidity groups at diagnosis was similar, higher comorbidity was associated with slower improvement in RA disease activity over the first year of treatment, likely driven by independent associations with patient and physician global assessments and pain.","PeriodicalId":21255,"journal":{"name":"Rheumatology","volume":"54 1","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rheumatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/rheumatology/keaf350","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
OBJECTIVES
Comorbidities negatively influence remission rates in rheumatoid arthritis (RA). This study estimated the effects of comorbidities on components of disease activity in early RA (ERA).
METHODS
Using the Rheumatic Disease Comorbidity Index (RDCI), the influence of comorbidities on trajectories of components of the SDAI (Simple Disease Activity Index) was assessed in participants with ERA enrolled in Canadian Early Arthritis Cohort (CATCH) over the first year of treatment. Adjusted effects of RDCI scores categorized 0, 1, 2, and ≥ 3 on SDAI trajectories over time were analyzed using multivariable generalized estimating equations (GEE) models adjusted for multiple confounders.
RESULTS
ERA participants (N = 2248) had a mean (SD) symptom duration of 5.7 (3) months; mean age 55 (15) years and 72% were female. Baseline SDAI was 29 (15), with 90% having moderate-high SDAI. Baseline RDCI scores were 0 in 888 (40%), 1 in 547 (24%), 2 in 451 (20%), and ≥3 in 362 (16%). While baseline disease activity was similar across comorbidity groups, patients with higher RDCI scores showed worse SDAI trajectories over the first year of RA treatment. Higher RDCI scores were independently associated with pain, patient and physician global assessments over time.
CONCLUSION
This large real-world analysis of ERA patients seen in routine rheumatology practice across Canada showed that while RA disease activity across comorbidity groups at diagnosis was similar, higher comorbidity was associated with slower improvement in RA disease activity over the first year of treatment, likely driven by independent associations with patient and physician global assessments and pain.
期刊介绍:
Rheumatology strives to support research and discovery by publishing the highest quality original scientific papers with a focus on basic, clinical and translational research. The journal’s subject areas cover a wide range of paediatric and adult rheumatological conditions from an international perspective. It is an official journal of the British Society for Rheumatology, published by Oxford University Press.
Rheumatology publishes original articles, reviews, editorials, guidelines, concise reports, meta-analyses, original case reports, clinical vignettes, letters and matters arising from published material. The journal takes pride in serving the global rheumatology community, with a focus on high societal impact in the form of podcasts, videos and extended social media presence, and utilizing metrics such as Altmetric. Keep up to date by following the journal on Twitter @RheumJnl.