Responsiveness of IGF-I and IGFBP-3 to therapeutic intervention in children and adolescents with Crohn's disease

被引:72
作者
Beattie, RM
Camacho-Hübner, C
Wacharasindhu, S
Cotterill, AM
Walker-Smith, JA
Savage, MO [1 ]
机构
[1] Univ London St Bartholomews Hosp Med Coll, Dept Endocrinol, Paediat Endocrinol Sect, London EC1A 7BE, England
[2] Univ London St Bartholomews Hosp Med Coll, Dept Chem Endocrinol, London EC1A 7BE, England
[3] Univ London St Bartholomews Hosp Med Coll, Dept Paediat Gastroenterol, London EC1A 7BE, England
关键词
D O I
10.1046/j.1365-2265.1998.00562.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE Abnormal linear growth is common in childhood and adolescent Crohn's disease. We have studied the concentrations of the inflammatory marker CRP and of serum IGF-I and IGFBP-3 in patients with active Crohn's disease and have assessed the changes in these parameters during therapeutic intervention with enteral nutrition or intestinal resection. DESIGN Children and adolescents attending the inflammatory bowel disease clinic at our hospital underwent treatment either with enteral nutrition (Study A) or intestinal resection (Study B). These are two separate studies and the results cannot be compared. Serum concentrations of CRP, IGF-I and IGFBP-3 were determined at 0, 2, 8 and 16 weeks after start of enteral nutrition and in addition to height velocity, at 0 and 6 months after intestinal resection. SUBJECTS Study A: 14 patients, 9 male, 5 female, median age 12.5 years (range 7.0-17.2), puberty stage 1 (n=13), stage 3 (n=1). Alt had active Crohn's disease. Study B: 9 patients, 7 male, 2 female, median age 13.5 years (range 7.8-16.5), puberty stage 1 (n=5), stages 2-4 (n=4). All had Crohn's disease resistant to medical therapy. METHODS Crohn's disease was confirmed radiologically, endoscopically and histologically. Disease activity was scored using the Lloyd Still index (LSI). Study A: nutritional support was with a polymeric, casein-based formula feed AL 110. Study B: surgical procedures were small bowel resection (n=2), right hemicolectomy (n=5), subtotal colectomy (n=2). MEASUREMENTS Study A: weight SDS, CRP, IGF-1 and IGFBP-3 were measured at 0, 2, 8, 16 weeks after start of enteral feeding. Study B: height velocity, CRP, IGF-I and IGFBP-3 were measured 0, 6 months after intestinal resection. STATISTICAL ANALYSIS Medians and ranges were used. Significance of changes was calculated using the Wilcoxon rank test for the analysis of paired data. RESULTS Study A: median LSI before treatment was 39 and increased after 8 weeks of enteral nutrition to 60 (P<0.05). Weight SDS increased at 8 and 16 weeks (P<0.05) compared to pretreatment CRP was elevated at 0 weeks, falling during treatment. Median (range) values (normal <5 mg/l) at 0 at 2, 8, 16 weeks were 53 mg/l (15-150), 8 mg/l (5-25), 7 mg/l (5-83) and 14 mg/l (5-39), all P<0.001 compared with pretreatment. Median IGF-I-values increased during treatment. Median (range) values at 0, 2, 8, 16 weeks (all P<0.005) compared to pretreatment, median (range) values at 0, 2, 8, 16 weeks were 78 mu g/l (50-204), 131 mu g/l (73-251), 119 mu g/l (77-291) and 133 mu g/l (67-497), all P<0.005 compared to pre-treatment. IGFBP-3 levels increased during treatment. Median (range) values at 0, 2, 8, 16 weeks were 2.4 mg/l (1.4-3.1), 2.9 mg/l (1.8-4.6), 3.0 mg/l, 3.2 mg/l (1.8-4.5), all P<0.01 compared to pretreatment. Study B: height velocity increased during 6 months after surgery. Median (range) values; 3.3 cm/year (0-8.3 ) before surgery, 8.4 cm/year (2-12.6) 6 months post-surgery, P<0.01. Median (range) CRP values fell from 45 mg/l (5-150) to 8 mg/l (5-31) and IGF-I-vatues increased from 163 mu g/l (64-286) to 226 mu g/l (71-391). These changes were not statistically significant. IGFBP-3 values did not change. CONCLUSION The IGF system, as shown by serum IGF-I and IGFBP-3, is responsive to therapeutic intervention in active Crohn's disease. It is likely that a combination of decreased inflammatory activity and improved nutrition contributes to these changes.
引用
收藏
页码:483 / 489
页数:7
相关论文
共 33 条
  • [1] BEATTIE RM, 1994, ALIMENT PHARM THERAP, V8, P609
  • [2] URINARY GROWTH-HORMONE IN GROWTH-IMPAIRED CHILDREN WITH CHRONIC INFLAMMATORY BOWEL-DISEASE
    BRAEGGER, CP
    TORRESANI, T
    MURCH, SH
    SAVAGE, MO
    WALKERSMITH, JA
    MACDONALD, TT
    [J]. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1993, 16 (01) : 49 - 52
  • [3] GROWTH AND PUBERTY IN CHRONIC INFLAMMATORY BOWEL-DISEASE
    BRAIN, CE
    SAVAGE, MO
    [J]. BAILLIERES CLINICAL GASTROENTEROLOGY, 1994, 8 (01): : 83 - 100
  • [4] TUMOR-NECROSIS-FACTOR ALPHA-PRODUCING CELLS IN THE INTESTINAL-MUCOSA OF CHILDREN WITH INFLAMMATORY BOWEL-DISEASE
    BREESE, EJ
    MICHIE, CA
    NICHOLLS, SW
    MURCH, SH
    WILLIAMS, CB
    DOMIZIO, P
    WALKERSMITH, JA
    MACDONALD, TT
    [J]. GASTROENTEROLOGY, 1994, 106 (06) : 1455 - 1466
  • [5] BREESE EJ, 1995, ALIMENT PHARM THERAP, V9, P547
  • [6] Cameron N., 1978, HUMAN GROWTH, DOI [10.1007/978-1-4684-2622-9_3, DOI 10.1007/978-1-4684-2622-9_3]
  • [7] CHRONIC INFLAMMATORY BOWEL-DISEASE IN CHILDHOOD
    CHONG, SKF
    BARTRAM, C
    CAMPBELL, CA
    WILLIAMS, CB
    BLACKSHAW, AJ
    WALKERSMITH, JA
    [J]. BRITISH MEDICAL JOURNAL, 1982, 284 (6309) : 101 - 103
  • [8] SURGERY FOR CROHNS-DISEASE IN CHILDHOOD - INFLUENCE OF SITE OF DISEASE AND OPERATIVE PROCEDURE ON OUTCOME
    DAVIES, G
    EVANS, CM
    SHAND, WS
    WALKERSMITH, JA
    [J]. BRITISH JOURNAL OF SURGERY, 1990, 77 (08) : 891 - 894
  • [9] Juvenile rheumatoid arthritis - Effects of disease activity and recombinant human growth hormone on insulin-like growth factor 1, insulin-like growth factor binding proteins 1 and 3, and osteocalcin
    Davies, UM
    Jones, J
    Reeve, J
    CamachoHubner, C
    Charlett, A
    Ansell, BM
    Preece, MA
    Woo, PMM
    [J]. ARTHRITIS AND RHEUMATISM, 1997, 40 (02): : 332 - 340
  • [10] Interleukin 6 causes growth impairment in transgenic mice through a decrease in insulin-like growth factor-I - A model for stunted growth in children with chronic inflammation
    DeBenedetti, F
    Alonzi, T
    Moretta, A
    Lazzaro, D
    Costa, P
    Poli, V
    Martini, A
    Ciliberto, G
    Fattori, E
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (04) : 643 - 650