Plasma interleukin-22 concentration and disease activity in inflammatory bowel disease.

Journal: Scientific reports
Published Date:

Abstract

The relationship between interleukin-22 and clinical characteristics of patients with inflammatory bowel disease is uncertain. We sought to determine whether plasma interleukin-22 concentrations are associated with disease activity in a large population of patients with inflammatory bowel disease. This was an observational study of patients with Crohn's disease or ulcerative colitis in the Study of a Prospective Adult Research Cohort with IBD (SPARC IBD) from the IBD Plexus registry of the Crohn's & Colitis Foundation in the United States. Interleukin-22 concentrations were measured using an R&D Systems human interleukin-22 enzyme-linked immunosorbent assay. Of 3993 patients included, 1604 with Crohn's disease and 836 with ulcerative colitis had non-missing interleukin-22 baseline samples, of which 33% and 25%, respectively, were above the lower limit of quantification (7.8 pg/mL). Significantly more patients with moderate/severe disease activity had high interleukin-22 concentrations (above lower limit of quantification) versus those with remission/mild disease activity (Crohn's disease: 44.7% vs. 30.0%, P < 0.00001; ulcerative colitis: 39.8% vs. 23.0%, P < 0.001). A multinomial logit model found approximately twice the odds of moderate/severe disease activity in those with high interleukin-22 versus low interleukin-22 (below lower limit of quantification). The strongest predictors of high interleukin-22 concentrations identified by a machine-learning algorithm were higher Short Crohn's Disease Activity Index score in patients with Crohn's disease and prescription of biologics in patients with ulcerative colitis. In summary, high interleukin-22 concentrations tended to be associated with higher disease activity in this large, real-world population of patients with inflammatory bowel disease.

Authors

  • Claudia Cabrera
    Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
  • Daniel Fernández-Llaneza
    Clinical Pharmacology and Safety Sciences, Biopharmaceuticals R&D, AstraZeneca, Pepparedsleden 1, 431 83, Mölndal, SE, Sweden. daniel.fernandez1@astrazeneca.com.
  • Marita Olsson
    Biometrics and Statistical Innovation, Late-Stage Development Respiratory & Immunology, AstraZeneca, Gothenburg, Sweden.
  • Charles Sopp
    BioPharmaceutical Medical, Real World Science & Analytics, AstraZeneca, Cambridge, UK.
  • Tara Fehlmann
    Crohn's & Colitis Foundation, New York, NY, USA.
  • Elizabeth A Duncan
    Late Respiratory and Immunology (R&I), BioPharmaceuticals R&D, AstraZeneca, Durham, NC, USA.
  • Emon Khan
    Late Respiratory and Immunology (R&I), BioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
  • Junmei Cairns
    Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN, USA.
  • Jessica Neisen
    Translational Science & Experimental Medicine, Research and Early Development, Respiratory and Immunology (R&I), BioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.
  • Ulf Gehrmann
    Translational Science & Experimental Medicine, Research and Early Development, Respiratory and Immunology (R&I), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Nick Powell
    Faculty of Medicine, Imperial College London, London, UK.