Ileal involvement is age dependent in pediatric Crohn's disease

被引:58
作者
Meinzer, U
Ideström, M
Alberti, C
Peuchmaur, M
Belarbi, N
Bellaïche, M
Mougenot, JF
Cézard, JP
Finkel, Y
Hugot, JP
机构
[1] Assistance Publ Hop Paris, Hop Robert Debre, Dept Paediat Gastroenterol, F-75019 Paris, France
[2] Hop Robert Debre, INSERM, U458, Programme Avenir, F-75019 Paris, France
[3] Karolinska Hosp, Astrid Lindgren Childrens Hosp, Dept Paediat Gastroenterol & Nutr, S-10401 Stockholm, Sweden
[4] Hop Robert Debre, INSERM, CIC EC, Dept Epidemiol & Stat, F-75019 Paris, France
[5] Univ Paris 07, Hop Robert Debre, EA3102, Dept Pathol, Paris, France
[6] Hop Robert Debre, Dept Radiol, F-75019 Paris, France
[7] Assistance Publ Hop Paris, Federat Interhosp Endoscopie Digest Pediat, Paris, France
关键词
CARD15; children; Crohn's disease; lymphoid follicle; NOD2; Peyer's patches;
D O I
10.1097/01.MIB.0000165114.10687.bf
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Lymphoid follicles (LFs) have been suggested to play a role at the early stage of Crohn's disease (CD) lesions. In the small bowel, Us are grouped, forming Peyer's patches, which develop early in fetal life, grow in size and number until puberty, and undergo involution. In contrast, colonic Us are isolated and undergo little change during life. As a result, if Us play a role in the occurrence of CD lesions, the distribution of ileal and colonic lesions is expected to be altered in small children. Methods: Medical records of 2 independent French (n = 136) and Swedish (n = 55) cohorts of consecutive pediatric CD were reviewed. Disease sites and age of onset were recorded, and the age-dependent probability to develop ileal lesions was computed. The CARD15/NOD2 genotype was also analyzed when available (n = 99). Results: The curves of disease occurrence were significantly different in case of CD with or without ileal lesions (P < 0.0001). At the age of 8 years, the probability (95% confidence interval) of small bowel involvement was 0.19 (0.07-0.39). It increased until 16 years of age to 0.61 (0.54-0.68). It was slightly higher in patients carrying I or more CARD15/NOD2 mutations [0.75 (0.55-0.89)] than in wildtype patients [0.46 (0.34-0.58)]. CAPD15 mutations also influenced the age of onset of ileal disease (P < 0.02). Conclusions: in children, ileal CD lesions are delayed compared with colonic lesions. This observation is in agreement with the previously proposed hypothesis of a pathophysiological role of Peyer's patches in ileal CD. The rarity of small bowel lesions should be a warning to be cautious when classifying chronic colitis in small children.
引用
收藏
页码:639 / 644
页数:6
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