P1048 - Inflammatory Bowel Disease-Associated Peripheral Spondyloarthritis (IBD-pSpA) Negatively Influences Health Related Quality of Life Across Multiple Patient Reported Outcomes - Results From the CHASE Cohort
Katherine Falloon, MD1, Suha Abushamma, MD1, Ashwin Ananthakrishnan, 2, Edward L. Barnes, MD, MPH3, Abhik Bhattacharya, MD4, Raymond K. Cross, MD, MS, FACG5, Shashank Cheemalavagu, MD1, Jean-Frederic Colombel, MD4, Emily Gore, MD4, Hans Herfarth, MD, PhD6, Sara Horst, MD, MPH, FACG7, M. Elaine Husni, MD1, Jeremy A.. Klein, MD8, Dana J. Lukin, MD, PhD, FACG9, Ellen J. Scherl, MD9, David T. Rubin, MD10, Benjamin L. Cohen, MD1, Taha Qazi, MD1, Qijun Yang, MS11, Brian G. Feagan, MD12, Florian Rieder, MD1 1Cleveland Clinic Foundation, Cleveland, OH; 2Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School, Boston, MA; 3Multidisciplinary Inflammatory Bowel Diseases Center, Division of Gastroenterology and Hepatology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA, Chapel Hill, NC; 4Icahn School of Medicine at Mount Sinai, New York, NY; 5The Melissa L. Posner Institute for Digestive Health & Liver Disease, Mercy Medical Center, Baltimore, MD; 6University of North Carolina at Chapel Hill, Chapel Hill, NC, USA, Chapel Hill, NC; 7Vanderbilt University School of Medicine, Nashville, TN; 8University of Chicago Medicine, Inflammatory Bowel Disease Center, Chicago, IL; 9Jill Roberts Center for Inflammatory Bowel Disease, Weill Cornell Medicine, New York, NY; 10University of Chicago Medicine Inflammatory Bowel Disease Center, Chicago, IL, USA, Chicago, IL; 11Cleveland Clinic, Cleveland, OH; 12Division of Gastroenterology, Department of Medicine, University of Western Ontario and Alimentiv, London, ON, Canada Introduction: Inflammatory bowel disease (IBD)-associated peripheral spondyloarthritis (IBD-pSpA) is common but not well studied, with limited data regarding impact on health-related quality of life (HRQoL). The aim of this study was to evaluate whether IBD-pSpA negatively impacts HRQoL via use of previously validated patient reported outcome measures (PROs). Methods: We prospectively recruited patients with IBD-pSpA, defined by previously established consensus criteria via the Cohort for Healing Arthritis, Skin, and Eye Extra-Intestinal Manifestations (CHASE-EIM), from six sites across the United States along with controls with IBD but no prior history of joint disease. All patients completed the Inflammatory Bowel Disease Questionnaire (IBDQ), the Work Productivity and Activity Impairment Questionnaire (WPAI), and the Functional Assessment of Chronic Illness Therapy – Fatigue (FACIT-F). Analyses were performed using R software and a significance level of 0.05 was assumed. Results: We recruited 235 patients (134 with IBD-pSpA and 101 controls with IBD but no history of joint disease). When compared with controls, patients with IBD-pSpA were older (median 43.2 [32.3; 53.8] vs 31.1 years [25.0; 39.9], p< 0.001), more often female (61.2% vs 46.0%, p=0.029), had longer disease duration (median 14.5 [7.50; 26.1] vs 9.0 years [3.65;1 5.4], p< 0.001), and were more likely to have CD (70.1% vs 54.0%, p=0.016). There were no statistically significant differences between groups with respect to IBD disease activity in the bowel as per global physician impression, endoscopy, or imaging (see Table 1), though patients with IBD-pSpA were statistically more likely to have an elevated CRP (30.4% vs 8.6%, p=0.024). They were also more likely to be on medications commonly used to treat IBD-pSpA (sulfasalazine and methotrexate, see Table 1). Patients with IBD-pSpA had statistically worsened WPAI scores across all domains (see Table 2). They also had lower median IBDQ scores (158 [127; 184]vs 185 [164; 204], p< 0.001) and lower FACIT-F scores (29 [19.0; 37.0] vs 42 [34.0; 47.0]) (Table 2). Discussion: The presence of IBD-pSpA is significantly associated with worsened HRQoL across multiple PRO domains, highlighting the need for further research to improve therapeutic management of this underserved patient population.
Figure: Table 1: Baseline Demographics and Clinical Characteristics
IBD = inflammatory bowel disease, UC = ulcerative colitis, CD = Crohn’s disease, CRP = C reactive protein
Figure: Table 2: Patient Reported Outcome Scores
WPAI = work productivity and activity impairment questionnaire, IBDQ = inflammatory bowel disease questionnaire, FACIT=F = functional assessment of chronic illness therapy
Katherine Falloon, MD1, Suha Abushamma, MD1, Ashwin Ananthakrishnan, 2, Edward L. Barnes, MD, MPH3, Abhik Bhattacharya, MD4, Raymond K. Cross, MD, MS, FACG5, Shashank Cheemalavagu, MD1, Jean-Frederic Colombel, MD4, Emily Gore, MD4, Hans Herfarth, MD, PhD6, Sara Horst, MD, MPH, FACG7, M. Elaine Husni, MD1, Jeremy A.. Klein, MD8, Dana J. Lukin, MD, PhD, FACG9, Ellen J. Scherl, MD9, David T. Rubin, MD10, Benjamin L. Cohen, MD1, Taha Qazi, MD1, Qijun Yang, MS11, Brian G. Feagan, MD12, Florian Rieder, MD1. P1048 - Inflammatory Bowel Disease-Associated Peripheral Spondyloarthritis (IBD-pSpA) Negatively Influences Health Related Quality of Life Across Multiple Patient Reported Outcomes - Results From the CHASE Cohort, ACG 2025 Annual Scientific Meeting Abstracts. Phoenix, AZ: American College of Gastroenterology.