Colonic Crohn's disease in children does not respond well to treatment with enteral nutrition if the ileum is not involved

被引:106
作者
Afzal, NA
Davies, S
Paintin, M
Arnaud-Battandier, F
Walker-Smith, JA
Murch, S
Heuschkel, R
Fell, J
机构
[1] Royal Free Hosp, Ctr Pediat Gastroenterol, London NW3 2QG, England
[2] Chelsea & Westminster Hosp, Dept Pediat Gastroenterol, London, England
[3] Nestle Res Ctr, CH-1000 Lausanne, Switzerland
关键词
Crohn's disease; child; enteral nutrition; colon;
D O I
10.1007/s10620-005-2864-6
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Data supporting a response to treatment with exclusive enteral nutrition in pediatric colonic Crohn's disease are few. We examined clinical and biochemical responses of ileal, colonic, and ileocolonic Crohn's disease and assessed the endoscopic and histological colonic mucosal response in the colonic and ileocolonic groups. We prospectively enrolled 65 children (age: 8-17 years) with acute intestinal Crohn's disease (Pediatric Crohn's Disease Activity Index [PCDAI] > 20). After ileocolonoscopy, gastroscopy, and a barium meal and follow-through, they were distributed into three groups (ileal, n = 12, ileocolonic, n = 39; and colonic, n = 14). All patients received exclusive polymeric feed as treatment, with a repeat endoscopy at completion of treatment. At enrollment the ileal group had significantly less severe disease (P = 0.05) compared to the colonic and ileocolonic groups. However, the colonic disease group showed the least fall in PCDAI scores at completion of treatment with enteral nutrition (P = 0.03), with the lowest remission rate (50%, vs 82.1% in the ileocolonic and 91.7% in the ileal group [chi(2) test, P = 0.021]). Endoscopic and histologic colonic mucosal assessment showed a posttreatment improvement in the ileocolonic (P <= 0.01) but not in the colonic disease group (P = ns). Children with disease in the colon respond better to enteral nutrition if the ileum is also involved. This may be due to different underlying inflammatory mechanisms. Detailed pretreatment assessment in studies of Crohn's disease according to disease distribution with appropriate individualized tailoring of treatment may be important in this regard.
引用
收藏
页码:1471 / 1475
页数:5
相关论文
共 32 条
[1]   Improvement in quality of life of children with acute Crohn's disease does not parallel mucosal healing after treatment with exclusive enteral nutrition [J].
Afzal, NA ;
van der Zaag-Loonen, HJ ;
Arnaud-Battandier, F ;
Davies, S ;
Murch, S ;
Derkx, B ;
Heuschkel, R ;
Fell, JM .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2004, 20 (02) :167-172
[2]  
AFZAL NA, 2002, CLIN NUTR S, P204
[3]   The molecular classification of the clinical manifestations of Crohn's disease [J].
Ahmad, T ;
Armuzzi, A ;
Bunce, M ;
Mulcahy-Hawes, K ;
Marshall, SE ;
Orchard, TR ;
Crawshaw, J ;
Large, O ;
De Silva, A ;
Cook, JT ;
Barnardo, M ;
Cullen, S ;
Welsh, KI ;
Jewell, DP .
GASTROENTEROLOGY, 2002, 122 (04) :854-866
[4]  
Andus T, 2000, HEPATO-GASTROENTEROL, V47, P29
[5]  
BEATTIE RM, 1994, ALIMENT PHARM THERAP, V8, P609
[6]   Bone mineral density and nutritional status in children with chronic inflammatory bowel disease [J].
Boot, AM ;
Bouquet, J ;
Krenning, EP ;
Keizer-Schrama, SMPFD .
GUT, 1998, 42 (02) :188-194
[7]   TUMOR-NECROSIS-FACTOR ALPHA-PRODUCING CELLS IN THE INTESTINAL-MUCOSA OF CHILDREN WITH INFLAMMATORY BOWEL-DISEASE [J].
BREESE, EJ ;
MICHIE, CA ;
NICHOLLS, SW ;
MURCH, SH ;
WILLIAMS, CB ;
DOMIZIO, P ;
WALKERSMITH, JA ;
MACDONALD, TT .
GASTROENTEROLOGY, 1994, 106 (06) :1455-1466
[8]   Long-term evolution of disease behavior of Crohn's disease [J].
Cosnes, J ;
Cattan, S ;
Blain, A ;
Beaugerie, L ;
Carbonnel, F ;
Parc, R ;
Gendre, JP .
INFLAMMATORY BOWEL DISEASES, 2002, 8 (04) :244-250
[9]   Early lesions of recurrent Crohn's disease caused by infusion of intestinal contents in excluded ileum [J].
D'Haens, GR ;
Geboes, K ;
Peeters, M ;
Baert, F ;
Pennickx, F ;
Rutgeerts, P .
GASTROENTEROLOGY, 1998, 114 (02) :262-267
[10]   The Crohn's disease-associated bacterial protein I2 is a novel enteric T cell superantigen [J].
Dalwadi, H ;
Wei, B ;
Kronenberg, M ;
Sutton, CL ;
Braun, J .
IMMUNITY, 2001, 15 (01) :149-158