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Gestational respiratory infections interacting with offspring HLA and CTLA-4 modifies incident β-cell autoantibodies

Lynch, Kristian F. (författare)
University of South Florida
Lee, Hye-Seung (författare)
University of South Florida
Törn, Carina (författare)
Lund University,Lunds universitet,Celiaki och diabetes,Forskargrupper vid Lunds universitet,Celiac Disease and Diabetes Unit,Lund University Research Groups,Skåne University Hospital
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Vehik, Kendra (författare)
University of South Florida
Krischer, Jeffrey P. (författare)
University of South Florida
Larsson, Helena Elding (författare)
Lund University,Lunds universitet,Pediatrisk endokrinologi,Forskargrupper vid Lunds universitet,Paediatric Endocrinology,Lund University Research Groups,Skåne University Hospital
Haller, Michael J (författare)
Florida Museum Natural History
Hagopian, William A. (författare)
Pacific Northwest Research Institute
Rewers, Marian J. (författare)
University of Colorado
She, Jin-Xiong (författare)
Medical College of Georgia
Simell, Olli G (författare)
Turku University Hospital
Toppari, Jorma (författare)
University of Turku
Ziegler, Anette G. (författare)
Klinikum rechts der Isar,Helmholtz Zentrum München
Akolkar, Beena (författare)
National Institute of Diabetes and Digestive and Kidney Diseases
Hyöty, Heikki (författare)
Bonifacio, Ezio (författare)
Lernmark, Åke (författare)
Lund University,Lunds universitet,Celiaki och diabetes,Forskargrupper vid Lunds universitet,Celiac Disease and Diabetes Unit,Lund University Research Groups,Skåne University Hospital
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 (creator_code:org_t)
 
Elsevier BV, 2018
2018
Engelska.
Ingår i: Journal of Autoimmunity. - : Elsevier BV. - 0896-8411. ; 86, s. 93-103
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • β-cell autoantibodies against insulin (IAA), GAD65 (GADA) and IA-2 (IA-2A) precede onset of childhood type 1 diabetes (T1D). Incidence of the first appearing β-cell autoantibodies peaks at a young age and is patterned by T1D-associated genes, suggesting an early environmental influence. Here, we tested if gestational infections and interactions with child's human leukocyte antigen (HLA) and non-HLA genes affected the appearance of the first β-cell autoantibody. Singletons of mothers without diabetes (n = 7472) with T1D-associated HLA-DR-DQ genotypes were prospectively followed quarterly through the first 4 years of life, then semiannually until age 6 years, using standardized autoantibody analyses. Maternal infections during pregnancy were assessed via questionnaire 3-4.5 months post-delivery. Polymorphisms in twelve non-HLA genes associated with the first appearing β-cell autoantibodies were included in a Cox regression analysis. IAA predominated as the first appearing β-cell autoantibody in younger children (n = 226, median age at seroconversion 1.8 years) and GADA (n = 212; 3.2 years) in children aged ≥2 years. Gestational infections were not associated with the first appearing β-cell autoantibodies overall. However, gestational respiratory infections (G-RI) showed a consistent protective influence on IAA (HR 0.64, 95% CI 0.45-0.91) among CTLA4-(AG, GG) children (G-RI*. CTLA4 interaction, p = 0.002). The predominant associations of HLA-DR-DQ 4-8/8-4 with IAA and HLA-DR-DQ 3-2/3-2 with GADA were not observed if a G-RI was reported (G-RI*HLA-DR-DQ interaction, p = 0.03). The role of G-RI may depend on offspring HLA and CTLA-4 alleles and supports a bidirectional trigger for IAA or GADA as a first appearing β-cell autoantibody in early life.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Nyckelord

Autoimmune diabetes
Autoimmunity
Glutamic acid decarboxylase
HLA
IA-2
Insulin
Type 1 diabetes
β-cell autoantibodies

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art (ämneskategori)
ref (ämneskategori)

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