Progression to diabetes in relatives with islet autoantibodies - Is it inevitable

Citation
Sg. Gardner et al., Progression to diabetes in relatives with islet autoantibodies - Is it inevitable, DIABET CARE, 22(12), 1999, pp. 2049-2054
Citations number
24
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
DIABETES CARE
ISSN journal
01495992 → ACNP
Volume
22
Issue
12
Year of publication
1999
Pages
2049 - 2054
Database
ISI
SICI code
0149-5992(199912)22:12<2049:PTDIRW>2.0.ZU;2-5
Abstract
OBJECTIVE - A large cohort of family members with islet cell antibodies (IC A) greater than or equal to 20 Juvenile Diabetes Foundation units (JDF U) w as examined to determine whether there was a subgroup at low risk of progre ssion to diabetes; whether risk of progression changed over lime; and wheth er rate of progression to diabetes varied according to age, islet autoantib odies, and generic markers of susceptibility. RESEARCH DESIGN AND METHODS - Individuals with ICA greater than or equal to 20 JDF I! were identified from 4,423 family members recruited to prospecti ve family studies in the U.K. Subjects were followed for up to 18 years. An tibodies to insulin, GAD, and IA-2 were measured in the first sample, and H LA class II typing was performed. RESULTS - Of 147 family members with ICA greater than or equal to 20 IDF U on at least one occasion, 29 developed type 1 diabetes after a median of 3. 2 years (maximum 18.1). The cumulative risk of developing diabetes within 1 5 years was 47% (95% CI 28-67) for all family members with ICA greater than or equal to 20 JDF U, 2.8% (0-8.2) for those with ICA alone, and 66% (44-8 7) for those with at least one additional autoantibody marker. There were n o differences in age, HLA class II tpc, or levels of ICA, insulin autoantib odies, or IA-2 antibodies between those who developed diabetes within 5 yea rs of testing and those who developed diabetes after this time. GAD antibod y levels were, however, higher in those who progressed more slowly CONCLUSIONS - Family members with ICA alone are at low risk of progression to diabetes. Rapid development of disease after ICA detection could nor be distinguished from delayed development on the basis of autoantibodies or ma rkers of genetic susceptibility, and those with multiple antibodies remaine d at high risk throughout long-term follow-up. This suggests that all famil y members with multiple islet autoantibodies are destined to develop autoim mune diabetes.