Prediction of type 1 diabetes in the general population.
Prediction of type 1 diabetes in the general population.
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DOI:
10.2337/dc09-1040
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发表时间:
2010-06
期刊:
影响因子:
16.2
通讯作者:
Akerblom HK
中科院分区:
文献类型:
--
作者:
Knip M;Korhonen S;Kulmala P;Veijola R;Reunanen A;Raitakari OT;Viikari J;Akerblom HK
To evaluate the utility of GAD antibodies (GADAs) and islet antigen-2 antibodies (IA-2As) in prediction of type 1 diabetes over 27 years in the general population and to assess the 6-year rates of seroconversion. A total of 3,475 nondiabetic subjects aged 3–18 years were sampled in 1980, and 2,375 subjects (68.3%) were resampled in 1986. All subjects were observed for development of diabetes to the end of 2007. GADAs and IA-2As were analyzed in all samples obtained in 1980 and 1986. A total of 34 individuals (1.0%; 9 developed diabetes) initially had GADAs and 22 (0.6%; 9 developed diabetes) IA-2As. Seven subjects (0.2%) tested positive for both autoantibodies. The positive seroconversion rate over 6 years was 0.4% for GADAs and 0.2% for IA-2As, while the inverse seroconversion rates were 33 and 57%, respectively. Eighteen subjects (0.5%) developed type 1 diabetes after a median pre-diabetic period of 8.6 years (range 0.9–20.3). Initial positivity for GADAs and/or IA-2As had a sensitivity of 61% (95% CI 36–83) for type 1 diabetes. Combined positivity for GADAs and IA-2As had both a specificity and a positive predictive value of 100% (95% CI 59–100). One-time screening for GADAs and IA-2As in the general childhood population in Finland would identify ∼60% of those individuals who will develop type 1 diabetes over the next 27 years, and those subjects who have both autoantibodies carry an extremely high risk for diabetes. Both positive and inverse seroconversions do occur over time reflecting a dynamic process of β-cell autoimmunity.
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影响因子:
8.2
作者:
Siljander, H. T.;Veijola, R.;Knip, M.
通讯作者:
Knip, M.
影响因子:
5.8
作者:
Kimpim채ki, T;Kupila, A;Knip, M
通讯作者:
Knip, M
影响因子:
16.2
作者:
LaGasse, JM;Palmer, JP;Monks, S
通讯作者:
Monks, S
影响因子:
8.2
作者:
BONIFACIO, E;GENOVESE, S;BOSI, E
通讯作者:
BOSI, E
影响因子:
8.2
作者:
Kulmala, P;Rahko, J;Knip, M
通讯作者:
Knip, M