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
[11]   T cell specificity and cross reactivity towards enterobacteria, Bacteroides, Bifidobacterium, and antigens from resident intestinal flora in humans [J].
Duchmann, R ;
May, E ;
Heike, M ;
Knolle, P ;
Neurath, M ;
zum Büschenfelde, KHM .
GUT, 1999, 44 (06) :812-818
[12]   The genetics of inflammatory bowel disease [J].
Duerr, RH .
GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 2002, 31 (01) :63-+
[13]  
Fell JME, 2000, ALIMENT PHARM THERAP, V14, P281
[14]   Application of the Vienna Classification for Crohn's disease to a single clinician database of 877 patients [J].
Freeman, HJ .
CANADIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2001, 15 (02) :89-93
[15]   Lessons from Nod2 studies: towards a link between Crohn's disease and bacterial sensing [J].
Girardin, SE ;
Hugot, JP ;
Sansonetti, PJ .
TRENDS IN IMMUNOLOGY, 2003, 24 (12) :652-658
[16]   Bone mineral density assessment in children with inflammatory bowel disease [J].
Gokhale, R ;
Favus, MJ ;
Karrison, T ;
Sutton, MM ;
Rich, B ;
Kirschner, BS .
GASTROENTEROLOGY, 1998, 114 (05) :902-911
[17]   Enteral nutrition and corticosteroids in the treatment of acute Crohn's disease in children [J].
Heuschkel, RB ;
Menache, CC ;
Megerian, JT ;
Baird, AE .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2000, 31 (01) :8-15
[18]   CARD15/NOD2 functions as an antibacterial factor in human intestinal epithelial cells [J].
Hisamatsu, T ;
Suzuki, M ;
Reinecker, HC ;
Nadeau, WJ ;
McCormick, BA ;
Podolsky, DK .
GASTROENTEROLOGY, 2003, 124 (04) :993-1000
[19]   Host recognition of bacterial muramyl dipeptide mediated through NOD2 [J].
Inohara, N ;
Ogura, Y ;
Fontalba, A ;
Gutierrez, O ;
Pons, F ;
Crespo, J ;
Fukase, K ;
Inamura, S ;
Kusumoto, S ;
Hashimoto, M ;
Foster, SJ ;
Moran, AP ;
Fernandez-Luna, JL ;
Nuñez, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :5509-5512
[20]   INFLUENCE OF INFLAMMATORY BOWEL-DISEASE ON INTESTINAL MICROFLORA [J].
KEIGHLEY, MRB ;
ARABI, Y ;
DIMOCK, F ;
BURDON, DW ;
ALLAN, RN ;
ALEXANDERWILLIAMS, J .
GUT, 1978, 19 (12) :1099-1104