[1型糖尿病患儿乳糜泻发生的预后因素]

Małgorzata Myśliwiec, Anna Balcerska, Jan Stepiński, Alicja Bakowska, Anna Jedrzejczyk, Joanna Bautembach-Minkowska, Beata Sztangierska, Piotr Banach, Piotr Wiśniewski
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引用次数: 0

摘要

前言:讨论了乳糜泻与1型糖尿病(DM1)共存的频率,并试图规范DM1患儿乳糜泻的诊断方法。目的:评估波兰波美拉尼亚地区DM1儿童乳糜泻的发病率,并分析这一特殊儿童群体中乳糜泻发展的推定预后因素。材料与方法:将70名年龄为9.47+/-4.59(第一组)的新发DM1患儿和223名年龄为10.20+/-3.87(诊断后4.47+/-3.16年)的长期1型糖尿病患儿纳入研究。检测c肽、HbA1c、CRP、TSH、fT4、fT3、尿白蛋白分泌率、IgA、抗麸质蛋白抗体(AGA)、抗组织转谷氨酰胺酶(TGA) IgA和IgG抗体(ELISA)、抗肌内膜(EmA) IgA和IgG抗体(免疫荧光)和抗酪蛋白抗体(TG)、抗甲状腺过氧化物酶(TPO)抗体(ELISA)水平。所有患者均行空肠活检和甲状腺超声检查。结果:基于空肠活检阳性,第1组患者中有5.7%被诊断为乳糜泻,而第2组为9.4%。2组TGA抗体阳性率为9.52%,AGA抗体阳性率为7.62%,EmA抗体阳性率为6.19%。10%的1组儿童有自身免疫性甲状腺炎,而24.2%的2组儿童有。长期DM1与乳糜泻同时存在的儿童组(A组)的特点是诊断年龄明显早(p=0.003), HbA(1)c较高(p=结论:DM1患儿空肠活检证实乳糜泻发病率高(9.4%)。血清TGA的评估似乎是DM1儿童乳糜泻检测最敏感的筛查标志物。
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[Prognostic factors of celiac disease occurrence in type 1 diabetes mellitus children].

Introduction: Discussion on the frequency of coexistent celiac disease and type 1 diabetes mellitus (DM1) as well as an attempt to standardize diagnostic methods of celiac disease detection among DM1 children have been performed.

Objectives: To assess the incidence of celiac disease among DM1 children in the Pomeranian region of Poland followed by analysis of the putative prognostic factors for celiac disease development in this particular group of children.

Materials and methods: 70 children aged 9.47+/-4.59 (group 1) de novo diagnosed with DM1 and 223 children aged 10.20+/-3.87 with long-standing diabetes mellitus type 1 (4.47+/-3.16 years from the diagnosis) were enrolled in the study. All the patients had C-peptide, HbA1c, CRP, TSH, fT4, fT3, urinary albumin secretion rate, IgA, level of antigliadin antibodies (AGA), anti-tissue transglutaminase (TGA) IgA and IgG antibodies (ELISA), anti-endomysium (EmA) IgA and IgG antibodies (immunofluorescence) and anti-tyreoglobulin antibodies (TG), anti-thyroid peroxidase (TPO) antibodies (ELISA) evaluated. All the patients had jejunal biopsy and thyroid ultrasound examination.

Results: 5.7% of group 1 patients were diagnosed with celiac disease based on the positive jejunal biopsy in comparison with 9.4% in the group 2. TGA antibodies were present in 9.52% of group 2, AGA in 7.62%, EmA in 6.19%. 10% of group 1 children had autoimmune thyroiditis versus 24.2% of group 2 children. The group of children with coincident long-lasting DM1 and celiac disease (group A) was characterized by significantly earlier age at diagnosis (p=0.003), higher HbA(1)c (p=<0.001), CRP (p<0.001) and elevated urine albumin secretion in relation to children without celiac disease and autoimmune thyroiditis (group B). Serologic test detecting TGA antibodies was found to be the most sensitive (95.2%) for the detection of celiac disease among DM1 children, while the lowest sensitivity was obtained in the case of the EmA antibody test (61.9%).

Conclusions: The celiac disease morbidity confirmed by jejunal biopsy is high among DM1 children (9.4%). The assessment of the serum TGA appears to be the most sensitive screening marker for the celiac disease detection in DM1 children.

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