ORIGINAL ARTICLE
Neurodevelopmental and neurological disorders in children and adolescents with type 1 diabetes in central Poland. A study on one heterogenous region of Poland
 
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1
Department of Paediatrics, Diabetology, Endocrinology and Nephrology, Medical University of Lodz, Lodz, Poland
 
2
Department of Paediatrics and Allergy, Medical University of Lodz, Lodz, Poland
 
3
Department of Rheumatology and Clinical Immunology with Internal Medicine Subdivision, University Clinical Hospital of the Military Academy of Medicine, Lodz, Poland
 
4
Department of Paediatrics, Oncology and Haematology, Medical University of Lodz, Lodz, Poland
 
 
Submission date: 2025-05-24
 
 
Final revision date: 2025-06-15
 
 
Acceptance date: 2026-05-06
 
 
Publication date: 2026-05-06
 
 
Corresponding author
Hanna Maria Kuśmierczyk-Kozieł   

Department of Pediatrics, Diabetology, Endocrinology and Nephrology, Medical University of Lodz, Poland
 
 
 
KEYWORDS
TOPICS
ABSTRACT
Introduction:
Some recent research has shown an increased prevalence of epilepsy and autism spectrum disorder (ASD) in children with type 1 diabetes (T1D) compared with the general population. This study aimed to evaluate the prevalence and clinical characteristics of the above-mentioned and other neurological disorders among children with T1D.

Material and methods:
The study included youths aged 1–16 with T1D from a single paediatric diabetes centre in Central Poland. Children with both T1D and neurological/neurodevelopmental diagnoses were identified by a retrospective medical records review of all patients. The prevalence was compared to the general prevalence among Polish children based on the official electronic databases.

Results:
The study comprised 669 children with T1D, mean age 11.23 ±3.43 years. Twenty nine (4.3%) had at least one neurological disorder, mostly epilepsy (12, 1.8%) and ASD (8, 1.2%). Nine participants had ≥ 1 neurological diagnosis. The prevalence of ASD among children with T1D was similar to the overall population patients aged ≤ 16 in Poland: 1.2% vs. 1.15% (OR = 1.044, 95% CI: 0.52–2.096, p = 0.9032), but it was higher for epilepsy: 1.8% vs. 1.02% (OR = 2.0112, 95% CI: 0.8427–4.7999, p = 0.11). Metabolic control in children with ASD was similar to those with T1D only, but significantly worse for other neurological disorders, especially epilepsy (HbA1c 7.9 ±1.6% vs. 7.2 ±1.0%, p = 0.0014 and 7.6 ±1.0% vs. 7.2 ±1.0%, p = 0.0029, respectively).

Conclusions:
In our study there is a small, but important group of individuals with T1D and neurological disorders comprising mostly boys. This group does not differ significantly from their peers with T1D only in terms of age or diabetes onset but has different immunological patterns and worse metabolic control.
REFERENCES (28)
1.
IDF Diabetes Atlas. 10th ed. Available from: www.diabetesatlas.org (accessed: 15.10.2022).
 
2.
Chobot A, Polanska J, Brandt A, Deja G, Glowinska-Olszewska B, Pilecki O, et al. Updated 24-year trend of type 1 diabetes incidence in children in Poland reveals a sinusoidal pattern and sustained increase. Diabet Med 2017; 34: 1252-1258.
 
3.
Battaglia M, Ahmed S, Anderson MS, Atkinson MA, Becker D, Bingley PJ, et al. Introducing the endotype concept to address the challenge of disease heterogeneity in type 1 diabetes. Diabetes Care 2020; 43: 5-12.
 
4.
Walendzik G, Nowak V. Wsparcie osób z autyzmem i zespołem Aspergera: przygotowanie do samodzielnego funkcjonowania. Kontrola Państw 2021; 66: 59-74.
 
5.
Ministerstwo Zdrowia. NFZ o zdrowiu. Padaczka. Avalable from: https://ezdrowie.gov.pl/portal... (accessed: 2020).
 
6.
Venny 2.1.0. Available from: https://bioinfogp.cnb.csic.es/... (accessed: 13.02.2024).
 
7.
Redondo MJ, Morgan NG. Heterogeneity and endotypes in type 1 diabetes mellitus. Nat Rev Endocrinol 2023; 19: 542-554.
 
8.
Hogendorf A, Lipska-Zietkiewicz BS, Szadkowska A, Borowiec M, Koczkowska M, Trzonkowski P, et al. Chromosome 18q deletion syndrome with autoimmune diabetes mellitus: putative genomic loci for autoimmunity and immunodeficiency. Pediatr Diabetes 2016; 17: 153-159.
 
9.
Hogendorf A, Zieliński M, Constantinou M, Śmigiel R, Wierzba J, Wyka K, et al. Immune dysregulation in patients with chromosome 18q deletions-searching for putative loci for autoimmunity and immunodeficiency. Front Immunol 2021; 12: 742834.
 
10.
Verrotti A, Scaparrotta A, Olivieri C, Chiarelli F. Seizures and type 1 diabetes mellitus: current state of knowledge. Eur J Endocrinol 2012; 167: 749-758.
 
11.
Dafoulas GE, Toulis KA, Mccorry D, Kumarendran B, Thomas GN, Willis BH, et al. Type 1 diabetes mellitus and risk of incident epilepsy: a population-based, open-cohort study. Diabetologia 2017; 60: 258-261. 12.
 
12.
De Sousa GJ, Tittel SR, Häusler M, Holterhus PM, Berger G, Holder M, et al. Type 1 diabetes and epilepsy in childhood and adolescence: do glutamic acid decarboxylase autoantibodies play a role? Data from the German/Austrian/Swiss/Luxembourgian DPV Registry. Pediatr Diabetes 2020; 21: 766-773.
 
13.
Wu S, Ding Y. Type 1 diabetes and the risk of epilepsy: a meta-analysis. J Diabetes Investig 2023; 15: 364-373.
 
14.
Amanat M, Thijs RD, Salehi M, Sander JW. Seizures as a clinical manifestation in somatic autoimmune disorders. Seizure 2019; 64: 59-64.
 
15.
Steriade C, Titulaer MJ, Vezzani A, Sander JW, Thijs RD. The association between systemic autoimmune disorders and epilepsy and its clinical implications. Brain 2021; 144: 372-390.
 
16.
Yoshimoto T, Doi M, Fukai N, Izumiyama H, Wago T, Minami I, et al. Type 1 diabetes mellitus and drug-resistant epilepsy: presence of high titer of anti-glutamic acid decarboxylase autoantibodies in serum and cerebrospinal fluid. Intern Med 2005; 44: 1174-1177.
 
17.
Bethin KE, Kanapka LG, Laffel LM, Majidi S, Chaytor NS, MacLeish S, et al. Autism spectrum disorder in children with type 1 diabetes. Diabet Med 2019; 36: 1282-1286.
 
18.
Freeman SJ, Roberts W, Daneman D. Type 1 diabetes and autism: Is there a link? Diabetes Care 2005; 28: 925-926.
 
19.
Tromans S, Yao G, Alexander R, Mukaetova-Ladinska E, Kiani R, Al-Uzri M, et al. The prevalence of diabetes in autistic persons: a systematic review. Clin Pract Epidemiol Ment Health 2020: 16: 212-225.
 
20.
Kohane IS, McMurry A, Weber G, MacFadden D, Rappaport L, Kunkel L, et al. The co-morbidity burden of children and young adults with autism spectrum disorders. PLoS One 2012; 7: e33224.
 
21.
Stanek KR, Youngkin EM, Pyle LL, Raymond JK, Driscoll KA, Majidi S. Prevalence, characteristics, and diabetes management in children with comorbid autism spectrum disorder and type 1 diabetes. Pediatr Diabetes 2019; 20: 645-651.
 
22.
Lemay JF, Lanzinger S, Pacaud D, Plener PL, Fürst-Burger A, Biester T, et al. Metabolic control of type 1 diabetes in youth with autism spectrum disorder: a multicenter Diabetes-Patienten-Verlaufsdokumentation analysis based on 61 749 patients up to 20 years of age. Pediatr Diabetes 2018; 19: 930-936.
 
23.
Zerbo O, Leong A, Barcellos L, Bernal P, Fireman B, Croen LA. Immune mediated conditions in autism spectrum disorders. Brain Behav Immun 2015; 46: 232.
 
24.
Chen MH, Su TP, Chen YS, Hsu JW, Huang KL, Chang WH, et al. Comorbidity of allergic and autoimmune diseases in patients with autism spectrum disorder: a nationwide population-based study. Res Autism Spectr Disord 2013; 7: 205-212.
 
25.
Bartolini E, Ferrari AR, Fiori S, Della Vecchia S. Glycaemic imbalances in seizures and epilepsy of paediatric age: a literature review. J Clin Med 2023; 12: 2580.
 
26.
Imad H, Johan Z, Eva K. Hypoglycemia and risk of seizures: a retrospective cross-sectional study. Seizure 2015; 25: 147-149.
 
27.
Oser TK, Oser SM, Parascando JA, Grisolano LA, Krishna KB, Hale DE, et al. Challenges and successes in raising a child with type 1 diabetes and autism spectrum disorder: mixed methods study. J Med Internet Res 2020; 22: e17184.
 
28.
Płatosa M (red.). Ogólnopolski spis autyzmu. Sytuacja młodzieży i dorosłych z autyzmem w Polsce. Stowarzyszenie Innowacji Społecznych „Mary i Max”, Warszawa 2016.
 
ISSN:2956-5812
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