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早期血清转化和快速增加的自身抗体浓度可预测遗传风险儿童的 1 型糖尿病青春期前发病。

Early seroconversion and rapidly increasing autoantibody concentrations predict prepubertal manifestation of type 1 diabetes in children at genetic risk.

机构信息

Department of Pediatrics, Turku University Hospital, Kiinamyllynkatu 4-8, PO Box 52, 20521 Turku, Finland.

出版信息

Diabetologia. 2012 Jul;55(7):1926-36. doi: 10.1007/s00125-012-2523-3. Epub 2012 Mar 23.

Abstract

AIMS/HYPOTHESIS: The aim of the study was to investigate the timing of the appearance of autoantibodies associated with type 1 diabetes between birth and puberty, the natural fate of these autoantibodies and the predictive power of autoantibody concentrations for early progression to clinical diabetes.

METHODS

Children were recruited to the Type 1 Diabetes Prediction and Prevention Project, an ongoing study based on HLA-conferred genetic risk. Autoantibodies against islet cells, insulin, GAD65 and islet antigen 2 were analysed at 3-12 month intervals, starting from birth.

RESULTS

During the follow-up, 1,320 children (18.4% of the cohort of 7,165 children) were autoantibody positive in at least one sample. Altogether, 184 autoantibody-positive children progressed to type 1 diabetes. Seroconversion occurred at an early age in the progressors (median 1.5 years), among whom 118 (64%) and 150 (82%) seroconverted to autoantibody positivity before the age of 2 and 3 years, respectively. The incidence of seroconversion peaked at 1 year of age. Compared with other autoantibody-positive children, the median autoantibody levels were already markedly higher 3 to 6 months after the seroconversion in children who later progressed to diabetes.

CONCLUSIONS/INTERPRETATION: Early initiation of autoimmunity and rapid increases in autoantibody titres strongly predict progression to overt diabetes before puberty, emphasising the importance of early life events in the development of type 1 diabetes.

摘要

目的/假设:本研究旨在探讨 1 型糖尿病相关自身抗体在出生至青春期之间出现的时间、这些自身抗体的自然转归以及自身抗体浓度对早期进展为临床糖尿病的预测能力。

方法

该研究招募了一批儿童参与 1 型糖尿病预测与预防项目,这是一项基于 HLA 遗传风险的正在进行的研究。从出生开始,每隔 3-12 个月检测一次胰岛细胞、胰岛素、GAD65 和胰岛抗原 2 的自身抗体。

结果

在随访期间,1320 名儿童(7165 名儿童队列的 18.4%)在至少一个样本中呈自身抗体阳性。共有 184 名自身抗体阳性儿童进展为 1 型糖尿病。进展者的自身抗体血清转化发生在较早的年龄(中位数 1.5 岁),其中 118 名(64%)和 150 名(82%)分别在 2 岁和 3 岁之前就发生了自身抗体阳性的血清转化。血清转化的发生率在 1 岁时达到峰值。与其他自身抗体阳性儿童相比,在后来进展为糖尿病的儿童中,自身抗体血清转化后 3 至 6 个月,自身抗体水平中位数已明显升高。

结论/解释:自身免疫的早期启动和自身抗体滴度的快速增加强烈提示在青春期前进展为显性糖尿病,这强调了生命早期事件在 1 型糖尿病发病机制中的重要性。

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