Yachha Surender K, Srivastava Anshu, Mohindra Samir, Krishnani Narendra, Aggarwal Rakesh, Saxena Anita
Department of Gastroenterology (Pediatric Gastroenterology), Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
J Gastroenterol Hepatol. 2007 Aug;22(8):1300-5. doi: 10.1111/j.1440-1746.2007.04929.x. Epub 2007 Jun 12.
BACKGROUND AND AIM: Follow-up studies on growth and histological recovery of children with celiac disease (CD) while on a gluten-free diet (GFD) are lacking from Asia. We therefore assessed the effects of this diet. METHODS: Forty-two children with CD were enrolled. Weight and height were expressed as weight for height (WfH) and height standard deviation scores (HSDS), respectively. Twenty-five children had repeated duodenal biopsies after 1-2 years and 14 had a third biopsy after 3-7 years of GFD. Compliance was checked by regular interview and IgA antiendomysial antibody estimation (EMA). RESULTS: At diagnosis (n = 25), mean HSDS was -3.3 +/- 1.6 with 76% having a HSDS of <-2; 60% were undernourished (WfH mean 81.6 +/- 5.7). Over a mean follow up of 3.7 years, HSDS improved to -1.3 +/- 1.7 and 84% cases achieved normal nutrition. Mean height velocity was 13.9 cm during first year and 5.6 cm in subsequent years. Small-bowel biopsies at diagnosis showed subtotal villous atrophy (Marsh IIIb) in 18 (72%) and partial villous atrophy (Marsh IIIa) in seven (28%) patients. Repeat biopsy at 1-2 years showed shift from subtotal to partial villous atrophy in 94% (n = 17/18) and normalization in one patient. In patients with Marsh IIIa improvement of partial villous atrophy was observed in all. Immunoglobulin A endomysial antibody was negative in 81%. Repeat biopsies at 5 years of GFD showed improvement to Marsh I-II, but none normalized. CONCLUSION: The majority of children with CD show normalization of nutrition and growth after GFD. Small-bowel histology improves markedly but does not normalize even after 5 years of GFD.
背景与目的:亚洲缺乏关于乳糜泻(CD)儿童在无麸质饮食(GFD)期间生长及组织学恢复情况的随访研究。因此,我们评估了这种饮食的效果。 方法:纳入42例CD儿童。体重和身高分别用身高体重比(WfH)和身高标准差评分(HSDS)表示。25例儿童在GFD 1 - 2年后进行了重复十二指肠活检,14例在GFD 3 - 7年后进行了第三次活检。通过定期访谈和IgA抗肌内膜抗体检测(EMA)检查依从性。 结果:诊断时(n = 25),平均HSDS为 - 3.3 ± 1.6,76%的儿童HSDS < - 2;60%营养不良(WfH平均为81.6 ± 5.7)。平均随访3.7年,HSDS改善至 - 1.3 ± 1.7,84%的病例营养状况恢复正常。第一年平均身高增长速度为13.9 cm,随后几年为5.6 cm。诊断时小肠活检显示,18例(72%)为全绒毛萎缩(马什IIIb型),7例(28%)为部分绒毛萎缩(马什IIIa型)。1 - 2年后重复活检显示,94%(n = 17/18)从全绒毛萎缩转变为部分绒毛萎缩,1例恢复正常。马什IIIa型患者的部分绒毛萎缩均有改善。81%的患者IgA抗肌内膜抗体呈阴性。GFD 5年后重复活检显示改善至马什I - II型,但无病例恢复正常。 结论:大多数CD儿童在GFD后营养和生长恢复正常。小肠组织学明显改善,但即使在GFD 5年后仍未恢复正常。
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