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Early-childhood body mass index and its association with the COVID-19 pandemic, containment measures and islet autoimmunity in children with increased risk for type 1 diabetes.
Hummel, Sandra; Rosenberger, Sarah; von dem Berge, Thekla; Besser, Rachel E J; Casteels, Kristina; Hommel, Angela; Kordonouri, Olga; Elding Larsson, Helena; Lundgren, Markus; Marcus, Benjamin A; Oltarzewski, Mariusz; Rochtus, Anne; Szypowska, Agnieszka; Todd, John A; Weiss, Andreas; Winkler, Christiane; Bonifacio, Ezio; Ziegler, Anette-G.
Afiliação
  • Hummel S; Institute of Diabetes Research, Helmholtz Munich, German Research Center for Environmental Health, Munich, Germany. sandra.hummel@helmholtz-munich.de.
  • Rosenberger S; Forschergruppe Diabetes e.V. at Helmholtz Zentrum München, Munich, Germany. sandra.hummel@helmholtz-munich.de.
  • von dem Berge T; School of Medicine, Forschergruppe Diabetes at Klinikum rechts der Isar, Technical University Munich, Munich, Germany. sandra.hummel@helmholtz-munich.de.
  • Besser REJ; Institute of Diabetes Research, Helmholtz Munich, German Research Center for Environmental Health, Munich, Germany.
  • Casteels K; Institute for Medical Information Processing, Biometry and Epidemiology - IBE, Ludwig-Maximilians-Universität München, Munich, Germany.
  • Hommel A; Pettenkofer School of Public Health, Munich, Germany.
  • Kordonouri O; Kinder- und Jugendkrankenhaus auf der Bult, Hannover, Germany.
  • Elding Larsson H; Centre for Human Genetics, JDRF/Wellcome Diabetes and Inflammation Laboratory, Nuffield Department of Medicine, NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.
  • Lundgren M; Department of Pediatrics, University Hospitals Leuven, Leuven, Belgium.
  • Marcus BA; Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
  • Oltarzewski M; Center for Regenerative Therapies Dresden, Technische Universität Dresden, Dresden, Germany.
  • Rochtus A; Paul Langerhans Institute Dresden of the Helmholtz Munich at University Hospital Carl Gustav Carus and Faculty of Medicine, Technische Universität Dresden, Dresden, Germany.
  • Szypowska A; Kinder- und Jugendkrankenhaus auf der Bult, Hannover, Germany.
  • Todd JA; Unit for Pediatric Endocrinology, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
  • Weiss A; Department of Paediatrics, Skane University Hospital, Malmö/Lund, Sweden.
  • Winkler C; Unit for Pediatric Endocrinology, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
  • Bonifacio E; Department of Pediatrics, Kristianstad Hospital, Kristianstad, Sweden.
  • Ziegler AG; School of Medicine, Forschergruppe Diabetes at Klinikum rechts der Isar, Technical University Munich, Munich, Germany.
Diabetologia ; 67(4): 670-678, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38214711
ABSTRACT
AIMS/

HYPOTHESIS:

The aim of this study was to determine whether BMI in early childhood was affected by the COVID-19 pandemic and containment measures, and whether it was associated with the risk for islet autoimmunity.

METHODS:

Between February 2018 and May 2023, data on BMI and islet autoimmunity were collected from 1050 children enrolled in the Primary Oral Insulin Trial, aged from 4.0 months to 5.5 years of age. The start of the COVID-19 pandemic was defined as 18 March 2020, and a stringency index was used to assess the stringency of containment measures. Islet autoimmunity was defined as either the development of persistent confirmed multiple islet autoantibodies, or the development of one or more islet autoantibodies and type 1 diabetes. Multivariate linear mixed-effect, linear and logistic regression methods were applied to assess the effect of the COVID-19 pandemic and the stringency index on early-childhood BMI measurements (BMI as a time-varying variable, BMI at 9 months of age and overweight risk at 9 months of age), and Cox proportional hazard models were used to assess the effect of BMI measurements on islet autoimmunity risk.

RESULTS:

The COVID-19 pandemic was associated with increased time-varying BMI (ß = 0.39; 95% CI 0.30, 0.47) and overweight risk at 9 months (ß = 0.44; 95% CI 0.03, 0.84). During the COVID-19 pandemic, a higher stringency index was positively associated with time-varying BMI (ß = 0.02; 95% CI 0.00, 0.04 per 10 units increase), BMI at 9 months (ß = 0.13; 95% CI 0.01, 0.25) and overweight risk at 9 months (ß = 0.23; 95% CI 0.03, 0.43). A higher age-corrected BMI and overweight risk at 9 months were associated with increased risk for developing islet autoimmunity up to 5.5 years of age (HR 1.16; 95% CI 1.01, 1.32 and HR 1.68, 95% CI 1.00, 2.82, respectively). CONCLUSIONS/

INTERPRETATION:

Early-childhood BMI increased during the COVID-19 pandemic, and was influenced by the level of restrictions during the pandemic. Controlling for the COVID-19 pandemic, elevated BMI during early childhood was associated with increased risk for childhood islet autoimmunity in children with genetic susceptibility to type 1 diabetes.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 4_TD Base de dados: MEDLINE Assunto principal: Ilhotas Pancreáticas / Diabetes Mellitus Tipo 1 / COVID-19 Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Humans Idioma: En Revista: Diabetologia Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 4_TD Base de dados: MEDLINE Assunto principal: Ilhotas Pancreáticas / Diabetes Mellitus Tipo 1 / COVID-19 Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Humans Idioma: En Revista: Diabetologia Ano de publicação: 2024 Tipo de documento: Article