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

被引:180
作者
Parikka, V. [1 ,2 ]
Nanto-Salonen, K. [1 ,2 ]
Saarinen, M. [3 ]
Simell, T. [1 ,2 ]
Ilonen, J. [4 ,5 ]
Hyoty, H. [6 ,7 ]
Veijola, R. [8 ,9 ]
Knip, M. [10 ,11 ,12 ,13 ]
Simell, O. [1 ,2 ]
机构
[1] Univ Turku, Dept Pediat, Turku, Finland
[2] Turku Univ Hosp, Dept Pediat, Turku 20521, Finland
[3] Univ Turku, Res Ctr Appl & Prevent Cardiovasc Med, Turku, Finland
[4] Univ Eastern Finland, Dept Clin Microbiol, Kuopio, Finland
[5] Univ Turku, Immunogenet Lab, Turku, Finland
[6] Univ Tampere, Dept Virol, FIN-33101 Tampere, Finland
[7] Tampere Univ Hosp, Ctr Lab Med, Dept Clin Microbiol, Tampere, Finland
[8] Oulu Univ Hosp, Dept Pediat, Oulu, Finland
[9] Univ Oulu, Dept Pediat, SF-90100 Oulu, Finland
[10] Univ Helsinki, Cent Hosp, Childrens Hosp, Helsinki, Finland
[11] Univ Helsinki, Inst Clin Med, Helsinki, Finland
[12] Folkhalsan Res Ctr, Helsinki, Finland
[13] Tampere Univ Hosp, Dept Pediat, Tampere, Finland
基金
芬兰科学院;
关键词
Autoantibodies; GADA; IA-2A; IAA; ICA; Type; 1; diabetes; ISLET-CELL ANTIBODIES; FINNISH CHILDREN; INCIDENCE TRENDS; RISING INCIDENCE; CLASS-I; INSULIN; CHILDHOOD; POPULATION; MELLITUS; PROGRESSION;
D O I
10.1007/s00125-012-2523-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1926 / 1936
页数:11
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