Serum Analyte Profiles Associated With Crohn's Disease and Disease Location

被引:18
作者
Boucher, Gabrielle [1 ]
Paradis, Alexandre [2 ]
Chabot-Roy, Genevieve [2 ]
Coderre, Lise [2 ]
Hillhouse, Erin E. [2 ]
Bitton, Alain [4 ]
Des Rosiers, Christine [1 ,3 ]
Levings, Megan K. [5 ]
Schumm, L. Philip [6 ]
Lazarev, Mark [7 ]
Brant, Steve R. [7 ,8 ,9 ,10 ,11 ,12 ,13 ]
Duerr, Richard [14 ]
McGovern, Dermot [15 ]
Silverberg, Mark S. [16 ]
Cho, Judy [17 ]
Lesage, Sylvie [2 ,18 ]
Rioux, John D. [1 ,19 ]
机构
[1] Montreal Heart Inst, Montreal, PQ, Canada
[2] Maisonneuve Rosemont Hosp, Res Ctr, Montreal, PQ, Canada
[3] McGill Univ, Div Gastroenterol, Montreal, PQ, Canada
[4] Univ Montreal, Dept Nutr, Montreal, PQ, Canada
[5] BC Childrens Hosp, Res Inst, Vancouver, BC, Canada
[6] Univ Chicago, Dept Publ Hlth Sci, Chicago, IL 60637 USA
[7] Johns Hopkins Univ, Sch Med, Dept Med, Harvey M & Lyn P Meyerhoff Inflammatory Bowel Dis, Baltimore, MD 21205 USA
[8] Rutgers State Univ, Rutgers Robert Wood Johnson Med Sch, Dept Med, Div Gastroenterol & Hepatol, New Brunswick, NJ USA
[9] Rutgers State Univ, Dept Genet, New Brunswick, NJ USA
[10] Rutgers State Univ, Human Genet Inst New Jersey, New Brunswick, NJ USA
[11] Rutgers State Univ, Rutgers Robert Wood Johnson Med Sch, Dept Med, Div Gastroenterol & Hepatol, Piscataway, NJ USA
[12] Rutgers State Univ, Dept Genet, Piscataway, NJ USA
[13] Rutgers State Univ, Human Genet Inst New Jersey, Piscataway, NJ USA
[14] Univ Pittsburgh, Dept Med, Pittsburgh, PA USA
[15] Cedars Sinai Med Ctr, F Widjaja Fdn Inflammatory Bowel & Immunobiol Res, Los Angeles, CA 90048 USA
[16] Mt Sinai Hosp, Mt Sinai Hosp Inflammatory Bowel Dis Ctr, Lunenfeld Tanenbaum Res Inst, Toronto, ON, Canada
[17] Mt Sinai, Icahn Sch Med, New York, NY USA
[18] Univ Montreal, Dept Microbiol Infectiol & Immunol, Montreal, PQ, Canada
[19] Univ Montreal, Dept Med, Montreal, PQ, Canada
基金
加拿大健康研究院; 加拿大创新基金会;
关键词
serum biomarkers; Crohn's disease; disease location; GENOME-WIDE ASSOCIATION; CHEMOKINE; IMMUNE; INFLAMMATION; ACTIVATION; DISCOVERY; GENETICS; POTENT; ALPHA; CELL;
D O I
10.1093/ibd/izab123
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Crohn's disease (CD) can affect any segment of the digestive tract but is most often localized in the ileal, ileocolonic, and colorectal regions of the intestines. It is believed that the chronic inflammation in CD is a result of an imbalance between the epithelial barrier, the immune system, and the intestinal microbiota. The aim of the study was to identify circulating markers associated with CD and/or disease location in CD patients. Methods: We tested 49 cytokines, chemokines, and growth factors in serum samples from 300 patients with CD and 300 controls. After quality control, analyte levels were tested for association with CD and disease location. Results: We identified 13 analytes that were higher in CD patients relative to healthy controls and that remained significant after conservative Bonferroni correction (P < 0.0015). In particular, CXCL9, CXCL1, and interleukin IL-6 had the greatest effect and were highly significant (P < 5 x 10(-7)). We also identified 9 analytes that were associated with disease location, with VEGF, IL-12p70, and IL-6 being elevated in patients with colorectal disease (P < 3 x 10(-4)). Conclusions: Multiple serum analytes are elevated in CD. These implicate the involvement of multiple cell types from the immune, epithelial, and endothelial systems, suggesting that circulating analytes reflect the inflammatory processes that are ongoing within the gut. Moreover, the identification of distinct profiles according to disease location supports the existence of a biological difference between ileal and colonic CD, consistent with previous genetic and clinical observations.
引用
收藏
页码:9 / 20
页数:12
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