Relationships between serum IGF-1, IGFBP-2, interleukin-1beta and interleukin-6 in inflammatory bowel disease

被引:93
作者
Street, ME
de'Angelis, G
Camacho-Hübner, C
Giovannelli, G
Ziveri, MA
Bacchini, PL
Bernasconi, S
Sansebastiano, G
Savage, MO [1 ]
机构
[1] St Bartholomews Hosp, Dept Endocrinol, London EC1A 7BE, England
[2] Univ Parma, Dept Paediat, I-43100 Parma, Italy
[3] Univ Parma, Dept Hyg, I-43100 Parma, Italy
关键词
insulin-like growth factor-I; insulin-like growth factor-binding protein-2 interleukin-1 beta; interleukin-6; inflammatory bowel disease; Crohn's disease; ulcerative colitis;
D O I
10.1159/000075699
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: To study the relationships between serum IGF-1, IGFBP-3 and IGFBP-2 and interleukin (IL)-1beta and IL-6 in inflammatory bowel disease (IBD). Methods: Thirty-seven patients (18 males, 19 females, aged 8.8 - 26.1 years) with IBD ( Crohn's disease, CD, n = 17, and ulcerative colitis, UC, n = 20) were studied. Patients were in relapse or remission according to established criteria. Serum IGF-1, IGFBP-3, IGFBP-2, IL-1beta and IL-6 levels were determined in patients and 15 healthy controls ( aged 8.2 - 19.0 years). Results: IGF-1 levels were lower in patients with CD in relapse compared with controls (p < 0.05). IGFBP-2 levels were higher in CD in relapse compared with other groups (all p < 0.05). In CD and UC patients ( n = 37), IGF-1 levels were inversely correlated with the erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP). IGFBP-2 levels correlated positively with ESR and IL-1beta. IL-6 levels correlated positively with ESR and CRP. IL-1beta levels were elevated in CD in relapse compared to controls (p < 0.05) and were higher in UC in relapse than in other groups ( all p < 0.05). In combined CD/UC patients in relapse (n = 20), IL-1beta levels were higher ( p < 0.05) in patients with recto-sigmoiditis ( n = 5) than in other patients. Conclusions: IGF-1, IGFBP-2 levels were related to IL levels, disease activity and anatomical distribution, consistent with active inflammation modifying the IGF-IGFBP system, possibly relevant to disturbance of growth. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:159 / 164
页数:6
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