Nutrients · 2018
Daily Intake of Milk Powder and Risk of Celiac Disease in Early Childhood: A Nested Case-Control Study.
СтатьяМногоцентровое исследованиеНаблюдательное исследованиеНазвание и аннотация: Перевод пока не подготовлен
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Hård Af Segerstad Elin M, Lee Hye-Seung, Andrén Aronsson Carin, Yang Jimin, Uusitalo Ulla, Sjöholm Ingegerd, Rayner Marilyn, Kurppa Kalle, Virtanen Suvi M, Norris Jill M, Agardh Daniel, TEDDY Study Group
Аннотация
Milk powder and gluten are common components in Swedish infants' diets. Whereas large intakes of gluten early in life increases the risk of celiac disease in genetically at-risk Swedish children, no study has yet evaluated if intake of milk powder by 2 years of age is associated with celiac disease. A 1-to-3 nested case-control study, comprised of 207 celiac disease children and 621 controls matched for sex, birth year, and HLA genotype, was performed on a birth cohort of HLA-DR3-DQ2 and/or DR4-DQ8-positive children. Subjects were screened annually for celiac disease using tissue transglutaminase autoantibodies (tTGA). Three-day food records estimated the mean intake of milk powder at ages 6 months, 9 months, 12 months, 18 months, and 24 months. Conditional logistic regression calculated odds ratios (OR) at last intake prior to seroconversion of tTGA positivity, and for each time-point respectively and adjusted for having a first-degree relative with celiac disease and gluten intake. Intake of milk powder prior to seroconversion of tTGA positivity was not associated with celiac disease (OR = 1.00; 95% CI = 0.99, 1.03; p = 0.763). In conclusion, intake of milk powder in early childhood is not associated with celiac disease in genetically susceptible children.
Предметные рубрики MeSH
Age of OnsetAutoantibodiesBiomarkersBottle FeedingCase-Control StudiesCeliac DiseaseChild, PreschoolEuropeFemaleGTP-Binding ProteinsGenetic Predisposition to DiseaseHLA-DQ AntigensHLA-DR3 AntigenHLA-DR4 AntigenHumansInfantInfant FormulaLogistic ModelsMaleOdds RatioPhenotypePowdersProspective StudiesProtein Glutamine gamma Glutamyltransferase 2Risk AssessmentRisk FactorsTransglutaminasesUnited States