Zachor D A, Mroczek-Musulman E, Brown P
Department of Pediatrics, University of Alabama at Birmingham, USA.
J Pediatr Gastroenterol Nutr. 2000 Sep;31(3):275-9. doi: 10.1097/00005176-200009000-00014.
Numerous studies in Europe have documented a high prevalence of celiac disease in Down syndrome. This study was undertaken to estimate the prevalence of celiac disease in Down syndrome in the southeastern United States.
Seventy-five patients with Down syndrome were screened using immunoglobulin (Ig)A-anti antiendomysium antibodies, IgA-antigliadin antibodies, and total IgA level. When either antiendomysium or antigliadin antibodies produced positive findings, patients were referred to a pediatric gastroenterologist for consideration of a duodenal biopsy.
Thirteen percent (10/75) were positive for antiendomysium antibodies. Half of these patients were also positive for antigliadin antibodies. Six of 10 patients positive for antiendomysium antibodies underwent intestinal biopsy. Changes consistent with celiac disease were documented in five. Histologic findings ranged from focal to total villous atrophy. None had IgA deficiency.
There was a high prevalence of positivity to antiendomysium antibody in Down syndrome. Antiendomysium antibody was a more sensitive screening test than antigliadin antibody. The prevalence of celiac disease in Down syndrome in the southeastern United States was 1 in 14 cases. Screening with antiendomysium antibody and IgA for all children with Down syndrome is recommended, even if there are no gastrointestinal symptoms.
欧洲的大量研究记录了唐氏综合征患者中乳糜泻的高患病率。本研究旨在估计美国东南部唐氏综合征患者中乳糜泻的患病率。
使用免疫球蛋白(Ig)A抗肌内膜抗体、IgA抗麦醇溶蛋白抗体和总IgA水平对75例唐氏综合征患者进行筛查。当抗肌内膜或抗麦醇溶蛋白抗体检测结果呈阳性时,患者会被转介给儿科胃肠病学家考虑进行十二指肠活检。
13%(10/75)的患者抗肌内膜抗体呈阳性。这些患者中有一半抗麦醇溶蛋白抗体也呈阳性。10例抗肌内膜抗体呈阳性的患者中有6例接受了肠道活检。其中5例记录到符合乳糜泻的变化。组织学表现从局灶性到完全绒毛萎缩不等。所有患者均无IgA缺乏。
唐氏综合征患者中抗肌内膜抗体阳性率较高。抗肌内膜抗体是比抗麦醇溶蛋白抗体更敏感的筛查试验。美国东南部唐氏综合征患者中乳糜泻的患病率为1/14。建议对所有唐氏综合征儿童进行抗肌内膜抗体和IgA筛查,即使没有胃肠道症状。