
Abstract Aims/hypothesis Delivery by Caesarean section continues to rise globally and has been associated with the risk of developing type 1 diabetes and the rate of progression from pre-symptomatic stage 1 or 2 type 1 diabetes to symptomatic stage 3 disease. The aim of this study was to examine the association between Caesarean delivery and progression to stage 3 type 1 diabetes in children with pre-symptomatic early-stage type 1 diabetes. Methods Caesarean section was examined in 8135 children from the TEDDY study who had an increased genetic risk for type 1 diabetes and were followed from birth for the development of islet autoantibodies and type 1 diabetes. Results The likelihood of delivery by Caesarean section was higher in children born to mothers with type 1 diabetes (adjusted OR 4.61, 95% CI 3.60, 5.90, p<0.0001), in non-singleton births (adjusted OR 4.35, 95% CI 3.21, 5.88, p<0.0001), in premature births (adjusted OR 1.91, 95% CI 1.53, 2.39, p<0.0001), in children born in the USA (adjusted OR 2.71, 95% CI 2.43, 3.02, p<0.0001) and in children born to older mothers (age group >28–33 years: adjusted OR 1.19, 95% CI 1.04, 1.35, p=0.01; age group >33 years: adjusted OR 1.80, 95% CI 1.58, 2.06, p<0.0001). Caesarean section was not associated with an increased risk of developing pre-symptomatic early-stage type 1 diabetes (risk by age 10 years 5.7% [95% CI 4.6%, 6.7%] for Caesarean delivery vs 6.6% [95% CI 6.0%, 7.3%] for vaginal delivery, p=0.07). Delivery by Caesarean section was associated with a modestly increased rate of progression to stage 3 type 1 diabetes in children who had developed multiple islet autoantibody-positive pre-symptomatic early-stage type 1 diabetes (adjusted HR 1.36, 95% CI 1.03, 1.79, p=0.02). No interaction was observed between Caesarean section and non-HLA SNPs conferring susceptibility for type 1 diabetes. Conclusions/interpretation Caesarean section increased the rate of progression to stage 3 type 1 diabetes in children with pre-symptomatic early-stage type 1 diabetes. Data availability Data from the TEDDY study (https://doi.org/10.58020/y3jk-x087) reported here will be made available for request at the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Central Repository (NIDDK-CR) Resources for Research (R4R) (https://repository.niddk.nih.gov/). Graphical Abstract
Short Communication ; Caesarean section ; Progression ; Type 1 diabetes ; Type 1 diabetes susceptibility genes, Male, Adult, Cesarean Section, Short Communication, Infant, Newborn, Infant, Newborn [MeSH] ; Female [MeSH] ; Disease Progression [MeSH] ; Adult [MeSH] ; Humans [MeSH] ; Progression ; Type 1 diabetes susceptibility genes ; Risk Factors [MeSH] ; Type 1 diabetes ; Autoantibodies/immunology [MeSH] ; Diabetes Mellitus, Type 1/genetics [MeSH] ; Male [MeSH] ; Caesarean section ; Short Communication ; Cesarean Section/adverse effects [MeSH] ; Child [MeSH] ; Pregnancy [MeSH] ; Child, Preschool [MeSH], Caesarean Section ; Progression ; Type 1 Diabetes ; Type 1 Diabetes Susceptibility Genes, Diabetes Mellitus, Type 1, Pregnancy, Risk Factors, Child, Preschool, Disease Progression, Humans, Female, Child, Autoantibodies, ddc: ddc:
Short Communication ; Caesarean section ; Progression ; Type 1 diabetes ; Type 1 diabetes susceptibility genes, Male, Adult, Cesarean Section, Short Communication, Infant, Newborn, Infant, Newborn [MeSH] ; Female [MeSH] ; Disease Progression [MeSH] ; Adult [MeSH] ; Humans [MeSH] ; Progression ; Type 1 diabetes susceptibility genes ; Risk Factors [MeSH] ; Type 1 diabetes ; Autoantibodies/immunology [MeSH] ; Diabetes Mellitus, Type 1/genetics [MeSH] ; Male [MeSH] ; Caesarean section ; Short Communication ; Cesarean Section/adverse effects [MeSH] ; Child [MeSH] ; Pregnancy [MeSH] ; Child, Preschool [MeSH], Caesarean Section ; Progression ; Type 1 Diabetes ; Type 1 Diabetes Susceptibility Genes, Diabetes Mellitus, Type 1, Pregnancy, Risk Factors, Child, Preschool, Disease Progression, Humans, Female, Child, Autoantibodies, ddc: ddc:
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