ESPE Abstracts (2024) 98 RFC15.4

ESPE2024 Rapid Free Communications Late Breaking (6 abstracts)

Autoimmunity in children with type 1 diabetes in association with the COVID_19 pandemic - results from the prospective DPV Registry

Claudia Boettcher 1 , Reinhard W Holl 2,3 , Katrin Nagl 4 , Beate Karges 5 , Simone Sengbusch 6 , Alena Welters 7 , Katharina Warncke 8,9 , Monika Flury 10 , Diyah Nahdiyati 11 , Thekla von dem Berge 12 & Clemens Kamrath 13


1University Children's Hospital, Julie-von-Jenner Haus, University of Bern, Paediatric Endocrinology and Diabetology, Bern, Switzerland. 2University of Ulm, Institute of Epidemiology and Medical Biometry, ZIBMT, Ulm, Germany. 3German Centre for Diabetes Research (DZD), Munich-Neuherberg, Germany. 4Medical University Vienna, Department of Pediatrics and Adolescent Medicine, Vienna, Austria. 5Medical Faculty, RWTH Aachen University, Division of Endocrinology and Diabetes, Aachen, Germany. 6Division of Peadiatric Endocrinology and Diabetology, University Medical Center Schleswig- Holstein, Campus Lübeck, University of Lübeck, Lübeck, Germany. 7Department of General Paediatrics, Neonatology and Paediatric Cardiology, Medical Faculty, University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany. 8Kinderklinik München Schwabing, School of Medicine, Technical University Munich, Department of Pediatrics, Munich, Germany. 9Helmholtz Munich, German Center for Environmental Health, Institute of Diabetes Research, Munich, Germany. 10Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Department of Paediatrics, Division of Paediatric Endocrinology and Diabetes, Dresden, Germany. 11Rehabilitation Centre for Children and Youth, Viktoriastift Clinic, Bad Kreuznach, Germany. 12Kinder- und Jugendkrankenhaus AUF DER BULT, Hannover, Germany. 13Centre for Paediatric and Adolescent Medicine, University of Freiburg, Section of Paediatric Endocrinology and Diabetology, Freiburg i. Br., Germany


Background and aim: Type 1 diabetes mellitus (T1D) is associated with other autoimmune diseases, often with a sex preference. The onset of the COVID-19 pandemic has led to reports on an increasing risk of autoimmune diseases. Our research aimed to investigate (concomitant) autoimmunity in children with T1D manifestation during the COVID-19 pandemic, considering gender and age, compared to pre-pandemic onset.

Methods: We analysed data of 21,654 children and adolescents aged 0.5-18 years without migration background from the DPV data pool with a T1D manifestation from 2015 to 2023. Rates of beta cell antibodies (ab) [IA2-, ZnT8-, GAD-, insulin-ab (max. four weeks after manifestation)], thyroid-, transglutaminase (TGA)-, and adrenal -ab were determined. Logistic regression models with age and gender as confounders served to investigate the influence of manifestation before (2015-19) versus during (2020-2023) the COVID-19 pandemic on endocrine autoimmunity.

Results: The included children and adolescents had a mean age of 9.6 years and a mean T1D duration of 0.34 years. 11,733 individuals had a T1D diagnosis before and 9,921 after the emergence of COVID-19. The table shows more population characteristics. T1D-onset after the beginning of the COVID-19 pandemic was associated with a higher rate of beta-cell autoimmunity, especially in IA2 (P <0.001 each), whilst there was a negative effect of the pandemic on ZnT8-ab (P <0.001), mainly in girls (P <0.0001). For GAD- and insulin-ab, no effects of the pandemic were seen. T1D-onset after the pandemic's beginning was negatively associated with adrenal-ab (P <0.0001). Neither thyroid- nor TGA-ab-positivity was associated with the COVID-19 pandemic.

Females Males Age
<6 6 - ≤ 12 12 - ≤ 18
N Mean N Mean N Mean N Mean N Mean
Age (y) 9,688 9.24 11,966 9.90 5,237 3.73 9,100 9.16 7,317 14.36
T1D duration (y) 9,688 0.34 11,966 0.33 5,237 0.32 9,100 0,34 7,317 0.34
BMI-SDS (KIGGS) 9,629 0.13 11,907 0.12 5,231 0.38 9,054 0.10 7,269 -0.03
Beta-cell + (%) 6,434 91.92 8,006 91.41 3,556 91.09 6,059 91.58 4,825 92.10
Thyroid-ab + (%) 6,815 10.79 8,474 5.05 3,664 3.08 6,469 7.45 5,156 10.99
TGA-ab + (%) 6,189 9.94 7,610 7.45 3,312 10.53 5,820 9.26 4,667 6.63
Adrenal-ab + (%) 680 5.88 760 4.47 361 6.37 637 4.55 442 4.98

Conclusion: The influence of the COVID-19 pandemic on beta-cell autoimmunity in children with new-onset T1D remains unclear. The COVID-19 pandemic does not seem to trigger the development of additional endocrine autoimmunity in children and adolescents with T1D.

Volume 98

62nd Annual ESPE (ESPE 2024)

Liverpool, UK
16 Nov 2024 - 18 Nov 2024

European Society for Paediatric Endocrinology 

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