Islet Autoantibody Seroconversion in the DPT-1 Study Justification for repeat screening throughout childhood

被引:16
|
作者
Vehik, Kendra [1 ]
Haller, Michael J. [2 ]
Beam, Craig A. [1 ]
Schatz, Desmond A. [2 ]
Wherrett, Diane K. [3 ]
Sosenko, Jay M. [4 ]
Krischer, Jeffrey P. [1 ]
机构
[1] Univ S Florida, Pediat Epidemiol Ctr, Tampa, FL 33620 USA
[2] Univ Florida, Coll Med, Gainesville, FL USA
[3] Univ Toronto, Hosp Sick Children, Dept Pediat, Div Endocrinol, Toronto, ON M5G 1X8, Canada
[4] Univ Miami, Div Endocrinol, Miami, FL USA
关键词
RELATIVES; INSULIN;
D O I
10.2337/dc10-1494
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-Although type 1 diabetes autoimmunity frequently begins in childhood, little is known about the relationship between age and autoimmunity development. Our aim was to determine the timing of seroconversion to diabetes-associated autoantibody (DAA) positivity and risk in first- and second-degree relatives of patients with type 1 diabetes. RESEARCH DESIGN AND METHODS-Study subjects were identified through the Diabetes Prevention Trial-Type 1 (DPT-1). Children 3-18 years of age (n = 42,447) were screened for DAAs; 1,454 were ICA positive (>= 10 JDF units), 1,758 were GAD65 positive, and 899 were ICA512 positive at the time of initial screening. Subjects who were initially antibody negative (n = 39,212) were recalled for rescreening, and 11,813 returned for rescreening. RESULTS-DAA seroconversion occurred in 469 (4%) children; 258 seroconverted to ICA, 234 to GAD65, and 99 to ICA512. The median time to seroconversion was 2 years. The 2-year risk for DAAs was highest in early childhood. For each 1-year increase in age in this cohort, the risk of any autoantibody seroconversion (HR 0.95, 95% CI 0.92-0.97) decreased by 5%, and for any two autoantibodies risk decreased by 13% (0.87, 0.82-0.93). CONCLUSIONS-Risk of autoantibody seroconversion among children followed in DPT-1 is age dependent. Younger children have the highest risk for DAAs, with the majority of children seroconverting by 13 years of age (75%). This suggests that annual screenings should be started in early childhood and continued through early adolescence to identify the majority of subjects at risk for type 1 diabetes and eligible for prevention trials.
引用
收藏
页码:358 / 362
页数:5
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