Comparison of immunological and immunogenetic markers in recent-onset type 1 diabetes among children and adults

Abstract This study aimed to compare the immunological and immunogenetic profiles over a spectrum of childhood- and adulthood-onset T1D at diagnosis. The cross-sectional study involved participants with recently diagnosed T1D (n = 168), aged 2.9–68.2 years. HLA-II alleles, single nucleotide polymorp...

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Main Authors: Kristi Alnek, Aili Tagoma, Kaja Metsküla, Ija Talja, Helis Janson, Maire Mandel, Tamara Vorobjova, Astrid Oras, Hanna Sepp, Katrin Pruul, Koit Reimand, Tiia Simonen, Aleksandr Peet, Ingrid Reppo, Kaia Tammiksaar, Maire Lubi, Kaire Heilman, Ülle Einberg, Kalle Kisand, Margus Lember, Vallo Tillmann, Raivo Uibo
Format: Article
Language:English
Published: Nature Portfolio 2025-05-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-99664-8
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author Kristi Alnek
Aili Tagoma
Kaja Metsküla
Ija Talja
Helis Janson
Maire Mandel
Tamara Vorobjova
Astrid Oras
Hanna Sepp
Katrin Pruul
Koit Reimand
Tiia Simonen
Aleksandr Peet
Ingrid Reppo
Kaia Tammiksaar
Maire Lubi
Kaire Heilman
Ülle Einberg
Kalle Kisand
Margus Lember
Vallo Tillmann
Raivo Uibo
author_facet Kristi Alnek
Aili Tagoma
Kaja Metsküla
Ija Talja
Helis Janson
Maire Mandel
Tamara Vorobjova
Astrid Oras
Hanna Sepp
Katrin Pruul
Koit Reimand
Tiia Simonen
Aleksandr Peet
Ingrid Reppo
Kaia Tammiksaar
Maire Lubi
Kaire Heilman
Ülle Einberg
Kalle Kisand
Margus Lember
Vallo Tillmann
Raivo Uibo
author_sort Kristi Alnek
collection DOAJ
description Abstract This study aimed to compare the immunological and immunogenetic profiles over a spectrum of childhood- and adulthood-onset T1D at diagnosis. The cross-sectional study involved participants with recently diagnosed T1D (n = 168), aged 2.9–68.2 years. HLA-II alleles, single nucleotide polymorphisms (SNP) (rs2476601, rs3087243, rs1990760, rs13266634), thyroid and coeliac disease-related autoantibodies and anti-enterovirus antibodies (anti-EV) were analysed regarding the diabetes-associated autoantibodies’ (DAA) status and the age of participants. In the longitudinal study, 19 immune checkpoint gene expression levels in children (n = 25) aged 3.6–14.5 years were measured at diagnosis and 1 year after diagnosis. The duration of symptoms before diagnosis was age-dependent. Older age increased the odds of being single DAA-positive (OR 1.05; 95% CI 1.02–1.09), while anti-EV IgG positivity increased the odds of being multiple DAA-positive (adjusted OR 4.42; 95% CI 1.62–12.04). The DAA-negative T1D participants were older than the DAA-positive individuals. The checkpoint gene expression levels between the two time points were similar, but exhibited more pronounced variability at the time of diagnosis. These results confirm immunological variability in recent-onset T1D cases between children and adults and stress the importance of further research to define the comprehensive immunological profile of the disease age-related subgroups.
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spelling doaj-art-0aa31c4baca34ac48c6d62522831a78e2025-08-20T02:10:53ZengNature PortfolioScientific Reports2045-23222025-05-0115111110.1038/s41598-025-99664-8Comparison of immunological and immunogenetic markers in recent-onset type 1 diabetes among children and adultsKristi Alnek0Aili Tagoma1Kaja Metsküla2Ija Talja3Helis Janson4Maire Mandel5Tamara Vorobjova6Astrid Oras7Hanna Sepp8Katrin Pruul9Koit Reimand10Tiia Simonen11Aleksandr Peet12Ingrid Reppo13Kaia Tammiksaar14Maire Lubi15Kaire Heilman16Ülle Einberg17Kalle Kisand18Margus Lember19Vallo Tillmann20Raivo Uibo21Department of Immunology, Institute of Bio- and Translational Medicine, University of TartuDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuChildren’s Clinic of Tartu University HospitalInternal Medicine Clinic of Tartu University HospitalInternal Medicine Clinic of Tartu University HospitalInternal Medicine Clinic of Tartu University HospitalTallinn Children’s HospitalTallinn Children’s HospitalDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuInternal Medicine Clinic of Tartu University HospitalChildren’s Clinic of Tartu University HospitalDepartment of Immunology, Institute of Bio- and Translational Medicine, University of TartuAbstract This study aimed to compare the immunological and immunogenetic profiles over a spectrum of childhood- and adulthood-onset T1D at diagnosis. The cross-sectional study involved participants with recently diagnosed T1D (n = 168), aged 2.9–68.2 years. HLA-II alleles, single nucleotide polymorphisms (SNP) (rs2476601, rs3087243, rs1990760, rs13266634), thyroid and coeliac disease-related autoantibodies and anti-enterovirus antibodies (anti-EV) were analysed regarding the diabetes-associated autoantibodies’ (DAA) status and the age of participants. In the longitudinal study, 19 immune checkpoint gene expression levels in children (n = 25) aged 3.6–14.5 years were measured at diagnosis and 1 year after diagnosis. The duration of symptoms before diagnosis was age-dependent. Older age increased the odds of being single DAA-positive (OR 1.05; 95% CI 1.02–1.09), while anti-EV IgG positivity increased the odds of being multiple DAA-positive (adjusted OR 4.42; 95% CI 1.62–12.04). The DAA-negative T1D participants were older than the DAA-positive individuals. The checkpoint gene expression levels between the two time points were similar, but exhibited more pronounced variability at the time of diagnosis. These results confirm immunological variability in recent-onset T1D cases between children and adults and stress the importance of further research to define the comprehensive immunological profile of the disease age-related subgroups.https://doi.org/10.1038/s41598-025-99664-8AdultsAutoantibodiesAutoantibody-negativeChildrenEnterovirus antibodiesHLA
spellingShingle Kristi Alnek
Aili Tagoma
Kaja Metsküla
Ija Talja
Helis Janson
Maire Mandel
Tamara Vorobjova
Astrid Oras
Hanna Sepp
Katrin Pruul
Koit Reimand
Tiia Simonen
Aleksandr Peet
Ingrid Reppo
Kaia Tammiksaar
Maire Lubi
Kaire Heilman
Ülle Einberg
Kalle Kisand
Margus Lember
Vallo Tillmann
Raivo Uibo
Comparison of immunological and immunogenetic markers in recent-onset type 1 diabetes among children and adults
Scientific Reports
Adults
Autoantibodies
Autoantibody-negative
Children
Enterovirus antibodies
HLA
title Comparison of immunological and immunogenetic markers in recent-onset type 1 diabetes among children and adults
title_full Comparison of immunological and immunogenetic markers in recent-onset type 1 diabetes among children and adults
title_fullStr Comparison of immunological and immunogenetic markers in recent-onset type 1 diabetes among children and adults
title_full_unstemmed Comparison of immunological and immunogenetic markers in recent-onset type 1 diabetes among children and adults
title_short Comparison of immunological and immunogenetic markers in recent-onset type 1 diabetes among children and adults
title_sort comparison of immunological and immunogenetic markers in recent onset type 1 diabetes among children and adults
topic Adults
Autoantibodies
Autoantibody-negative
Children
Enterovirus antibodies
HLA
url https://doi.org/10.1038/s41598-025-99664-8
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