4.7 Article

Serum 25-Hydroxyvitamin D Concentrations in Children Progressing to Autoimmunity and Clinical Type 1 Diabetes

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 101, Issue 2, Pages 723-729

Publisher

ENDOCRINE SOC
DOI: 10.1210/jc.2015-3504

Keywords

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Funding

  1. Juvenile Diabetes Research Foundation [4-1998-274, 4-1999-731, 4-2001-435]
  2. Academy of Finland (Centre of Excellence in Molecular Systems Immunology and Physiology Research) [250114, 284597]
  3. Funds for University Hospitals in Finland
  4. Sigrid Juselius Foundation
  5. Signe and Ane Gyllenberg Foundation
  6. Finnish Diabetes Research Foundation
  7. Jalmari and Rauha Ahokas Foundation
  8. University of Turku Doctoral Programme of Clinical Investigation
  9. Academy of Finland (AKA) [284597, 284597] Funding Source: Academy of Finland (AKA)

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Context: The role of vitamin D in the development of type 1 diabetes (T1D) remains controversial. Objective: The objective of the investigation was to study whether there are detectable differences in serum 25-hydroxyvitamin D (25[OH]D) concentrations between children who later progressed to T1D (cases) and matched children who remained nondiabetic and negative for islet autoantibodies (controls) when followed up from birth until disease onset. Design: A total of 3702 prospective serum samples from 252 children were measured for 25(OH)D from the age of 3 months onward using an enzyme immunoassay. Differences between the groups were compared by the mixed-model analysis of variance. Setting: T1D prediction and prevention study clinics in Turku, Oulu, and Tampere University Hospitals, Finland, participated in the study. Participants: By the end of 2012, all 126 case children were diagnosed with T1D. The control children (n = 126) were matched for age, sex, study site, and human leukocyte antigen-HLA-DQ-conferred risk for T1D. Main Outcome Measure: Median circulating 25(OH)D concentration (nanomoles per liter) was measured. Results: The patterns of variation in circulating 25(OH)D concentrations were similar between cases and controls and did not correlate with the age at seroconversion to autoantibody positivity (P = .79) or disease onset (P = .13). The median concentration of all collected samples did not differ between case and control children (66.6 nmol/L [range 14.0-262.8] vs 67.4 nmol/L [range 19.9-213.0]) P = .56). Conclusions: This study shows that serum 25(OH)D concentrations are not associated with the development of T1D in Finland.

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