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首页> 外文期刊>Diabetes care >Age at development of type 1 diabetes- and celiac disease-associated antibodies and clinical disease in genetically susceptible children observed from birth.
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Age at development of type 1 diabetes- and celiac disease-associated antibodies and clinical disease in genetically susceptible children observed from birth.

机译:从出生开始就观察到的遗传易感儿童中1型糖尿病和腹腔疾病相关抗体的发展年龄和临床疾病。

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OBJECTIVE: To compare the ages and sequence in which antibodies associated with type 1 diabetes and celiac disease appear and overt diseases develop in children with an HLA-conferred susceptibility to both diseases. RESEARCH DESIGN AND METHODS: We observed 2,052 children carrying genetic risks for both type 1 diabetes and celiac disease from birth until the median age of 5.7 years and analyzed diabetes- and celiac disease-associated antibodies in serum samples collected at 3- to 12-month intervals. Diabetes was confirmed by World Health Organization criteria and celiac disease by duodenal biopsies. RESULTS: Altogether 342 children seroconverted to positivity for at least one diabetes-associated autoantibody and 88 to positivity for at least one celiac disease-associated antibody at the median ages of 3.0 and 1.5 years, respectively (P < 0.001). If only children with biochemically defined diabetes-associated autoantibodies against insulin, GAD, or IA-2A protein (n = 146) and children with tissue transglutaminase autoantibodies were compared (n = 86), the median seroconversion ages were 2.5 and 3.0 years (P = 0.011). Fifty-one children progressed to overt diabetes at 4.5 years and 44 children to celiac disease at 4.3 years (P = 0.257). Of the 19 children who developed both diabetes- and celiac disease-associated antibodies, 3 progressed to both diabetes and celiac disease. CONCLUSIONS: Children with HLA-conferred susceptibility to type 1 diabetes and celiac disease develop celiac disease-associated antibodies mostly at a younger age or the same age at which they develop diabetes-associated autoantibodies. Clinical diabetes and celiac disease are commonly diagnosed at the same median age.
机译:目的:比较与HLA相关的两种疾病易感性患儿与1型糖尿病和腹腔疾病相关的抗体出现和显性疾病发展的年龄和顺序。研究设计和方法:我们观察了2052名从出生到中位年龄为5.7岁的儿童均患有1型糖尿病和乳糜泻的遗传风险,并分析了在3到12个月收集的血清样本中与糖尿病和乳糜泻相关的抗体间隔。根据世界卫生组织的标准确认为糖尿病,通过十二指肠活检确认为乳糜泻。结果:在中位年龄分别为3.0岁和1.5岁的儿童中,共有342名儿童血清阳性转化为至少一种与糖尿病相关的自身抗体,而对于至少一种腹腔疾病相关抗体血清转化为88例(P <0.001)。如果仅对患有胰岛素,GAD或IA-2A蛋白的生化定义与糖尿病相关的自身抗体的儿童(n = 146)和具有组织转谷氨酰胺酶自身抗体的儿童(n = 86)进行比较,则血清转化年龄的中位数分别为2.5岁和3.0岁(P = 0.011)。 51名儿童在4.5岁时患上了明显的糖尿病,而44名儿童在4.3岁时患了乳糜泻(P = 0.257)。在19位同时患有糖尿病和腹腔疾病相关抗体的儿童中,有3位同时患有糖尿病和腹腔疾病。结论:患有HLA的1型糖尿病和腹腔疾病易感儿童大多会在与糖尿病相关的自身抗体的年龄较小或相同的年龄发展与腹腔疾病相关的抗体。临床糖尿病和腹腔疾病通常被诊断为相同的中位年龄。

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