Increased serum levels of YKL-40 in patients with inflammatory bowel disease

被引:81
作者
Koutroubakis, IE
Petinaki, E
Dimoulios, P
Vardas, E
Roussomoustakaki, M
Maniatis, AN
Kouroumalis, EA
机构
[1] Univ Hosp Heraklion, Dept Gastroenterol, Iraklion 71110, Crete, Greece
[2] Univ Thessaly, Lab Clin Microbiol, Iraklion, Crete, Greece
关键词
Crohn's disease; fibroblast; fibrosis; inflammation; ulcerative colitis;
D O I
10.1007/s00384-002-0446-z
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and aims: Initiation of a fibrotic process has been suggested as part of the intestinal response to chronic inflammation in inflammatory bowel disease. YKL-40 has been proposed as a new serum marker of fibrosis. We studied compared the serum levels of YKL-40 in patients with ulcerative colitis or Crohn's disease with inflammatory and healthy controls. Patients and methods: YKL-40 serum levels were measured in 179 patients with inflammatory bowel disease (94 ulcerative colitis, 85 Crohn's disease), in 23 with intestinal inflammation of other causes, and 70 matched healthy controls using a commercially available enzyme-linked immunosorbent assay. YKL-40 levels were assessed in terms of disease activity, type and localization. Results: Mean serum YKL-40 levels were 102.6+/-82.7 ng/ml in ulcerative colitis patients and 112.2+/-83.7 ng/ml in Crohn's disease patients, significantly higher than in healthy controls (64.1+/-21.4 ng/ml) but not significantly different from inflammatory controls (77.8+/-23.1 ng/ml). Disease activity and C-reactive protein levels were significantly correlated with YKL-40 levels in both ulcerative colitis and Crohn's disease. Crohn's disease patients with ileum localization had significantly higher YKL-40 levels than those with ileocolonic or colonic disease. Patients with stenotic disease had mean YKL-40 levels not significantly different than those with nonstenotic disease. Conclusion: Serum levels of YKL-40 are increased in patients with inflammatory bowel disease, and this is associated with the inflammatory process rather than with the degree of fibrosis.
引用
收藏
页码:254 / 259
页数:6
相关论文
共 26 条
[1]  
Baslund B, 1998, ARTHRITIS RHEUM, V41, pS118
[2]  
BEST WR, 1976, GASTROENTEROLOGY, V70, P439
[3]   YKL-40 (cartilage gp-39) induces proliferative events in cultured chondrocytes and synoviocytes and increases glycosaminoglycan synthesis in chondrocytes [J].
De Ceuninck, F ;
Gaufillier, S ;
Bonnaud, A ;
Sabatini, M ;
Lesur, C ;
Pastoureau, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 285 (04) :926-931
[4]   Strictures in Crohn's disease are characterised by an accumulation of mast cells colocalised with laminin but not with fibronectin or vitronectin [J].
Gelbmann, CM ;
Mestermann, S ;
Gross, V ;
Köllinger, M ;
Schölmerich, J ;
Falk, W .
GUT, 1999, 45 (02) :210-217
[5]  
HAKALA BE, 1993, J BIOL CHEM, V268, P25803
[6]  
Johansen JS, 1996, BRIT J RHEUMATOL, V35, P553
[7]   Plasma YKL-40: A new potential marker of fibrosis in patients with alcoholic cirrhosis? [J].
Johansen, JS ;
Moller, S ;
Price, PA ;
Bendtsen, F ;
Junge, J ;
Garbarsch, C ;
Henriksen, JH .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1997, 32 (06) :582-590
[8]  
JOHANSEN JS, 1992, J BONE MINER RES, V7, P501
[9]   Inflammation location, but not type, determines the increase in TGF-β1 and IGF-1 expression and collagen deposition in IBD intestine [J].
Lawrance, IC ;
Maxwell, L ;
Doe, W .
INFLAMMATORY BOWEL DISEASES, 2001, 7 (01) :16-26
[10]   Altered response of intestinal mucosal fibroblasts to profibrogenic cytokines in inflammatory bowel disease [J].
Lawrance, IC ;
Maxwell, L ;
Doe, W .
INFLAMMATORY BOWEL DISEASES, 2001, 7 (03) :226-236