Evidence map›Paper›PMID 38214711›Full record

ArticleDiabetologia2024

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.

Sandra Hummel, Sarah Rosenberger, Thekla von dem Berge, Rachel E J Besser, Kristina Casteels, Angela Hommel, Olga Kordonouri, Helena Elding Larsson, Markus Lundgren, Benjamin A Marcus and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Diabetologia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.9field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 8 institutions in 5 countries.

Sandra HummelInstitute of Diabetes Research, Helmholtz Munich, German Research Center for Environmental Health, Munich, Germany. sandra.hummel@helmholtz-munich.de.ORCID 0000-0001-6554-5974
Sarah RosenbergerInstitute of Diabetes Research, Helmholtz Munich, German Research Center for Environmental Health, Munich, Germany.
Thekla von dem BergeKinder- und Jugendkrankenhaus auf der Bult, Hannover, Germany.
Rachel E J BesserCentre for Human Genetics, JDRF/Wellcome Diabetes and Inflammation Laboratory, Nuffield Department of Medicine, NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.
Kristina CasteelsDepartment of Pediatrics, University Hospitals Leuven, Leuven, Belgium.
Angela HommelCenter for Regenerative Therapies Dresden, Technische Universität Dresden, Dresden, Germany.
Olga KordonouriKinder- und Jugendkrankenhaus auf der Bult, Hannover, Germany.
Helena Elding LarssonUnit for Pediatric Endocrinology, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
Markus LundgrenUnit for Pediatric Endocrinology, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
Benjamin A MarcusSchool of Medicine, Forschergruppe Diabetes at Klinikum rechts der Isar, Technical University Munich, Munich, Germany.
Mariusz OltarzewskiDepartment of Paediatric Diabetology and Paediatrics, The Children's Clinical Hospital Józef Polikarp Brudziński, Warsaw, Poland.
Anne RochtusDepartment of Pediatrics, University Hospitals Leuven, Leuven, Belgium.
Agnieszka SzypowskaDepartment of Paediatric Diabetology and Paediatrics, The Children's Clinical Hospital Józef Polikarp Brudziński, Warsaw, Poland.
John A ToddCentre for Human Genetics, JDRF/Wellcome Diabetes and Inflammation Laboratory, Nuffield Department of Medicine, NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.
Andreas WeissInstitute of Diabetes Research, Helmholtz Munich, German Research Center for Environmental Health, Munich, Germany.
Christiane WinklerInstitute of Diabetes Research, Helmholtz Munich, German Research Center for Environmental Health, Munich, Germany.
Ezio BonifacioCenter for Regenerative Therapies Dresden, Technische Universität Dresden, Dresden, Germany.
Anette-G ZieglerInstitute of Diabetes Research, Helmholtz Munich, German Research Center for Environmental Health, Munich, Germany.
GPPAD and POInT Study Group
Helmholtz Zentrum München · DETUM Klinikum · DECentre for Human Genetics · GBKinderkrankenhaus auf der Bult · DEKU Leuven · BELund University · SEMedical University of Warsaw · PLPaul Langerhans Institute Dresden · DE

Funding

Wellcome TrustWellcome Trust [107212/Z/15/Z]
6 · The paper itself

Abstract

aims/hypothesisThe 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.

methodsBetween 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.

resultsThe COVID-19 pandemic was associated with increased time-varying BMI (β = 0.39; 95% CI 0.30, 0.47) and overweight risk at 9 months (β = 0.44; 95% CI 0.03, 0.84). During the COVID-19 pandemic, a higher stringency index was positively associated with time-varying BMI (β = 0.02; 95% CI 0.00, 0.04 per 10 units increase), BMI at 9 months (β = 0.13; 95% CI 0.01, 0.25) and overweight risk at 9 months (β = 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/

interpretationEarly-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.

Indexed as

COVID-19Diabetes Mellitus, Type 1Islets of LangerhansAutoantibodiesAutoimmunityBody Mass IndexChild, PreschoolHumansOverweightPandemicsAutoantibodiesChildhood BMICOVID-19Islet autoimmunityStringency indexType 1 diabetes

Identifiers

PMID38214711
PMCPMC10904508
OpenAlexW4390793613

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.