Systemic interleukin-9 in inflammatory bowel disease: Association with mucosal healing in ulcerative colitis

AIM To evaluate circulating IL9 in inflammatory bowel disease and disease-associated anemia/cachexia and assess its potential as a mucosal healing marker.METHODS Serum IL9 as well as other cytokines(IL1β, IL6, IL13, IFNγ, TNFα, and VEGF-A) were determined in 293 individuals: 97 patients with Crohn’s...

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Published in:World journal of gastroenterology : WJG Vol. 23; no. 22; pp. 4039 - 4046
Main Authors: Matusiewicz, Malgorzata, Neubauer, Katarzyna, Bednarz-Misa, Iwona, Gorska, Sabina, Krzystek-Korpacka, Malgorzata
Format: Journal Article
Language:English
Published: United States Baishideng Publishing Group Inc 14-06-2017
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Summary:AIM To evaluate circulating IL9 in inflammatory bowel disease and disease-associated anemia/cachexia and assess its potential as a mucosal healing marker.METHODS Serum IL9 as well as other cytokines(IL1β, IL6, IL13, IFNγ, TNFα, and VEGF-A) were determined in 293 individuals: 97 patients with Crohn’s disease(CD) and 74 with ulcerative colitis(UC) and in 122 apparently healthy controls. The clinical activity of CD and UC was expressed in terms of the Crohn’s Disease Activity Index(CDAI) and the Mayo Scoring System(MDAI), respectively, and the severity of bowel inflammation in UC patients was assessed using Mayo endoscopic score. Cytokine concentrations were measured by a flow cytometry-based method using Luminex x MAP? technology. Highsensitive C-reactive protein concentrations(hs CRP) were determined in CD and UC patients using the enhanced immunoturbidimetric method.RESULTS Systemic IL9 was significantly lower in healthy individuals [9 pg/m L(95%CI: 8.2-10)] than in patients with inflammatory bowel disease(IBD): both inactive [14.3 pg/m L(11.9-19.9)] and active (27.6 pg/m L(24.5-32), P < 0.0001)Cytokine concentrations were significantly higher in active CD [27.4 pg/m L(23.4-32.2)] and in active UC [32.7 pg/m L(27-38.9)] compared to inactive diseases (15.9 pg/m L(10.8-23.4) in CD and 19.4 pg/m L(13.9-27.1) in UC, P = 0.001)IL9 correlated weakly with CDAI(ρ = 0.32, P = 0.003) and MDAI(ρ = 0.35, P = 0.002) and strongly with endoscopic inflammation in UC(ρ = 0.74, P < 0.0001). As a negative marker of mucosal healing(MH), IL9 had an accuracy superior to hs CRP and IL6 (97%(P < 0.0001), 67%(P = 0.071), and 55%(P = 0.525), respectively)IL9 was significantly higher in cachectic IBD patients [30.25 pg/m L(24.4-37.5) vs 21.88 pg/m L(18-26.5), P = 0.026] and negatively correlated with hemoglobin concentrations(ρ =-0.27, P < 0.001). Multiple regression showed IL1β and IL13 to be the independent predictors of circulating IL9 in healthy individuals, IFNγ or IL6 in active and inactive UC, respectively, and IL13 and VEGF-A in both active and inactive CD.CONCLUSION The systemic IL9 level is higher in IBD and corresponds with endoscopic inflammation, suggesting its possible application as a negative marker of mucosal healing in UC.
Bibliography:Malgorzata Matusiewicz;Katarzyna Neubauer;Iwona Bednarz-Misa;Sabina Gorska;Malgorzata Krzystek-Korpacka;Department of Medical Biochemistry, Wroclaw Medical University;Department of Gastroenterology and Hepatology, Wroclaw Medical University;Laboratory of Medical Microbiology, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences
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Author contributions: Matusiewicz M and Krzystek-Korpacka M designed research; Neubauer K treated patients and collected material and clinical data from patients; Matusiewicz M, Bednarz-Misa I, Gorska S and Krzystek-Korpacka M performed the assays; Matusiewicz M and Krzystek-Korpacka M conducted statistical analyses; Matusiewicz M, Neubauer M and Krzystek-Korpacka M analysed and interpreted data; Matusiewicz M and Krzystek-Korpacka M wrote the paper; all authors critically revised the paper and approved its final version.
Correspondence to: Malgorzata Krzystek-Korpacka, PhD, DSc (Med), Department of Medical Biochemistry, Wroclaw Medical University, ul. Chalubinskiego 10, 50-368 Wroclaw, Poland. malgorzata.krzystek-korpacka@umed.wroc.pl
Supported by National Science Center, No. DEC-2011/01/D/NZ5/02835.
Telephone: +48-71-7841395 Fax: + 48-71-7840085
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v23.i22.4039