On the road to universal screening for risk of type 1 diabetes.
On the road to universal screening for risk of type 1 diabetes.
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DOI:
10.1016/s2213-8587(22)00166-8
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发表时间:
2022-08
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Mohamed Ghalwash and colleagues1 sought to determine the optimal age or ages for islet-autoantibody screening to predict the development of clinical type 1 diabetes by 15 years of age. The authors combined five birth cohorts (from the DIPP cohort in Finland, DiPiS cohort in Sweden, DAISY cohort in Colorado, USA, DEW-IT cohort in Washington, USA, and BABYDIAB cohort in Germany) with a total of approximately 25 000 children at risk for type 1 diabetes. The analysis focused on almost 7000 of these participants, who had been followed up to age 15 years or, in about 10% of the cases, developed clinical type 1 diabetes. Data from the remaining children, with shorter follow-up, were used to mitigate the potential bias caused by non-random loss of follow-up, by applying inverse probability censoring weighting, a method that accounts for right-censored outcomes. The relative homogeneity of the study samples and available data allowed harmonisation of the five studies, and the resulting large size of the combined dataset is one of the strengths of the analysis. Autoantibodies to insulin, GAD65, and IA-2 were tested at several, varying timepoints.The major novel finding in this study is that testing for islet autoantibodies at 2 years and 6 years of age had the highest sensitivity (82%) and positive predictive value (79%) for diabetes by age 15 years. That is, 82% of the individuals who developed type 1 diabetes by age 15 years were identified by the autoantibody screening strategy proposed by the authors, and 79% of the participants identified as being autoantibody positive ultimately developed the disease. This performance seems acceptable for a screening strategy, in which