TY - JOUR
T1 - Brief communication
T2 - Early appearance of islet autoantibodies predicts childhood type 1 diabetes in offspring of diabetic parents
AU - Hummel, Michael
AU - Bonifacio, Ezio
AU - Schmid, Sandra
AU - Walter, Markus
AU - Knopff, Annette
AU - Ziegler, Anette G.
PY - 2004/6/1
Y1 - 2004/6/1
N2 - Background: The development of type 1 diabetes mellitus is preceded by autoimmunity against islet β cells. Objective: To determine the risk for islet autoimmunity and childhood diabetes in offspring of affected parents. Design: Prospective cohort study. Setting: German BABYDIAB study. Participants: 1610 offspring of parents with type 1 diabetes. Measurements: Autoantibodies to islet autoantigens were measured at 9 months, 2 years, 5 years, and 8 years of age. Results: By 5 years of age, the frequency of islet autoantibodies was 5.9% (95% CI, 4.6% to 7.2%), the frequency of multiple islet autoantibodies was 3.5% (CI, 2.5% to 4.5%), and the frequency of diabetes was 1.5% (CI, 0.9% to 2.1%). The risk for diabetes was highest in offspring with multiple autoantibodies (40% within 5 years vs. 3% in offspring with single autoantibodies; P = 0.005). Progression to multiple islet autoantibodies was fastest in children who were autoantibody positive by age 2 years (P < 0.001), and progression to diabetes was inversely related to the age of positivity for multiple autoantibodies (P = 0.02). Limitations: The findings are limited to childhood diabetes in affected families. Conclusions: Childhood autoimmune diabetes is associated with autoimmunity that starts before 2 years of age.
AB - Background: The development of type 1 diabetes mellitus is preceded by autoimmunity against islet β cells. Objective: To determine the risk for islet autoimmunity and childhood diabetes in offspring of affected parents. Design: Prospective cohort study. Setting: German BABYDIAB study. Participants: 1610 offspring of parents with type 1 diabetes. Measurements: Autoantibodies to islet autoantigens were measured at 9 months, 2 years, 5 years, and 8 years of age. Results: By 5 years of age, the frequency of islet autoantibodies was 5.9% (95% CI, 4.6% to 7.2%), the frequency of multiple islet autoantibodies was 3.5% (CI, 2.5% to 4.5%), and the frequency of diabetes was 1.5% (CI, 0.9% to 2.1%). The risk for diabetes was highest in offspring with multiple autoantibodies (40% within 5 years vs. 3% in offspring with single autoantibodies; P = 0.005). Progression to multiple islet autoantibodies was fastest in children who were autoantibody positive by age 2 years (P < 0.001), and progression to diabetes was inversely related to the age of positivity for multiple autoantibodies (P = 0.02). Limitations: The findings are limited to childhood diabetes in affected families. Conclusions: Childhood autoimmune diabetes is associated with autoimmunity that starts before 2 years of age.
UR - http://www.scopus.com/inward/record.url?scp=2542505445&partnerID=8YFLogxK
U2 - 10.7326/0003-4819-140-11-200406010-00009
DO - 10.7326/0003-4819-140-11-200406010-00009
M3 - Article
C2 - 15172902
AN - SCOPUS:2542505445
SN - 0003-4819
VL - 140
SP - 882-886+I-64
JO - Annals of Internal Medicine
JF - Annals of Internal Medicine
IS - 11
ER -