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1.
Eur J Nutr ; 63(4): 1329-1338, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38413484

ABSTRACT

PURPOSE: The aim was to study the association between dietary intake of B vitamins in childhood and the risk of islet autoimmunity (IA) and progression to type 1 diabetes (T1D) by the age of 10 years. METHODS: We followed 8500 T1D-susceptible children born in the U.S., Finland, Sweden, and Germany in 2004 -2010 from the Environmental Determinants of Diabetes in the Young (TEDDY) study, which is a prospective observational birth cohort. Dietary intake of seven B vitamins was calculated from foods and dietary supplements based on 24-h recall at 3 months and 3-day food records collected regularly from 6 months to 10 years of age. Cox proportional hazard models were adjusted for energy, HLA-genotype, first-degree relative with T1D, sex, and country. RESULTS: A total of 778 (9.2) children developed at least one autoantibody (any IA), and 335 (3.9%) developed multiple autoantibodies. 280 (3.3%) children had IAA and 319 (3.8%) GADA as the first autoantibody. 344 (44%) children with IA progressed to T1D. We observed that higher intake of niacin was associated with a decreased risk of developing multiple autoantibodies (HR 0.95; 95% CI 0.92, 0.98) per 1 mg/1000 kcal in niacin intake. Higher intake of pyridoxine (HR 0.66; 95% CI 0.46, 0.96) and vitamin B12 (HR 0.87; 95% CI 0.77, 0.97) was associated with a decreased risk of IAA-first autoimmunity. Higher intake of riboflavin (HR 1.38; 95% CI 1.05, 1.80) was associated with an increased risk of GADA-first autoimmunity. There were no associations between any of the B vitamins and the outcomes "any IA" and progression from IA to T1D.  CONCLUSION: In this multinational, prospective birth cohort of children with genetic susceptibility to T1D, we observed some direct and inverse associations between different B vitamins and risk of IA.


Subject(s)
Autoantibodies , Autoimmunity , Diabetes Mellitus, Type 1 , Islets of Langerhans , Vitamin B Complex , Humans , Diabetes Mellitus, Type 1/immunology , Diabetes Mellitus, Type 1/epidemiology , Male , Female , Vitamin B Complex/administration & dosage , Prospective Studies , Child , Child, Preschool , Infant , Islets of Langerhans/immunology , Autoantibodies/blood , Risk Factors , Diet/methods , Diet/statistics & numerical data , Proportional Hazards Models , United States/epidemiology , Finland/epidemiology , Sweden/epidemiology , Germany/epidemiology , Dietary Supplements , Birth Cohort , Disease Progression
2.
Nutrients ; 11(8)2019 Aug 02.
Article in English | MEDLINE | ID: mdl-31382440

ABSTRACT

Probiotics are linked to positive regulatory effects on the immune system. The aim of the study was to examine the association between the exposure of probiotics via dietary supplements or via infant formula by the age of 1 year and the development of celiac disease autoimmunity (CDA) and celiac disease among a cohort of 6520 genetically susceptible children. Use of probiotics during the first year of life was reported by 1460 children. Time-to-event analysis was used to examine the associations. Overall exposure of probiotics during the first year of life was not associated with either CDA (n = 1212) (HR 1.15; 95%CI 0.99, 1.35; p = 0.07) or celiac disease (n = 455) (HR 1.11; 95%CI 0.86, 1.43; p = 0.43) when adjusting for known risk factors. Intake of probiotic dietary supplements, however, was associated with a slightly increased risk of CDA (HR 1.18; 95%CI 1.00, 1.40; p = 0.043) compared to children who did not get probiotics. It was concluded that the overall exposure of probiotics during the first year of life was not associated with CDA or celiac disease in children at genetic risk.


Subject(s)
Celiac Disease/epidemiology , Probiotics/administration & dosage , Autoimmune Diseases/epidemiology , Autoimmune Diseases/genetics , Celiac Disease/genetics , Celiac Disease/immunology , Child , Child, Preschool , Dietary Supplements , Female , Genetic Predisposition to Disease , Genotype , HLA Antigens/genetics , Humans , Infant , Infant Formula , Infant, Newborn , Male , Risk Factors
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