4.3 Article

Vitamin D status, enterovirus infection, and type 1 diabetes in Italian children/adolescents

期刊

PEDIATRIC DIABETES
卷 19, 期 5, 页码 923-929

出版社

WILEY
DOI: 10.1111/pedi.12673

关键词

adolescents; children; enterovirus; infection; PCR; type 1 diabetes; vitamin D

资金

  1. JDRF nPOD-V [25-2012-770]
  2. Italian Ministry of Health [PE-2013-02357094]

向作者/读者索取更多资源

At the time of the clinical onset of type 1 diabetes (T1D), we investigated 82 pediatric cases in parallel with 117 non-diabetic controls matched by age, geographic area, and time of collection. The occurrence of an enteroviral infection was evaluated in peripheral blood using a sensitive method capable of detecting virtually all human enterovirus (EV) types. While non-diabetic controls were consistently EV-negative, 65% of T1D cases carried EVs in blood. The vitamin D status was assessed by measuring the concentration of 25-hydroxyvitamin D [25(OH)D] in serum. Levels of 25(OH)D were interpreted as deficiency (<= 50 nmol/L), insufficiency (52.5-72.5 nmol/L), and sufficiency (75-250 nmol/L). In T1D cases, the median serum concentration of 25(OH)D was 54.4 +/- 27.3 nmol/L vs 74.1 +/- 28.5 nmol/L in controls (P=.0001). Diabetic children/adolescents showed deficient levels of vitamin D 25(OH)D (ie, 72.5 nmol/L) in 48.8% cases vs 17.9% in non-diabetic controls (P=.0001). Unexpectedly, the median vitamin D concentration was significantly reduced in virus-positive vs virus-negative diabetics (48.2 +/- 22.5 vs 61.8 +/- 31.2 nmol/L; P=.015), with deficient levels in 58.5% vs 31.0%, respectively. Thus, at the time of clinical onset, EV-positive cases had reduced vitamin D levels compared with EV-negative cases. This could indicate either that the virus-negative children/adolescents had been hit by a non-infectious T1D-triggering event, or that children/adolescents with proper levels of vitamin D had been able to rapidly clear the virus. Thus, it would be important to assess whether adequate vitamin D supplementation before or during the prediabetic phase of T1D may counteract the diabetogenic potential of infectious pathogens.

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