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A pilot interventional study to evaluate the impact of cholecalciferol treatment on HbA1c in type 1 diabetes (T1D).
Perchard, R; Magee, L; Whatmore, A; Ivison, F; Murray, P; Stevens, A; Mughal, M Z; Ehtisham, S; Campbell, J; Ainsworth, S; Marshall, M; Bone, M; Doughty, I; Clayton, P E.
Afiliación
  • Perchard R; Division of Developmental Biology & MedicineSchool of Medical Sciences, Faculty of Biology, Medicine & Health, University of Manchester, Manchester, UK.
  • Magee L; Division of Developmental Biology & MedicineSchool of Medical Sciences, Faculty of Biology, Medicine & Health, University of Manchester, Manchester, UK.
  • Whatmore A; Division of Developmental Biology & MedicineSchool of Medical Sciences, Faculty of Biology, Medicine & Health, University of Manchester, Manchester, UK.
  • Ivison F; Department of BiochemistryCentral Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
  • Murray P; Division of Developmental Biology & MedicineSchool of Medical Sciences, Faculty of Biology, Medicine & Health, University of Manchester, Manchester, UK.
  • Stevens A; Department of Paediatric EndocrinologyRoyal Manchester Children's Hospital, Central Manchester Foundation Hospitals NHS Trust, Manchester, UK.
  • Mughal MZ; Division of Developmental Biology & MedicineSchool of Medical Sciences, Faculty of Biology, Medicine & Health, University of Manchester, Manchester, UK.
  • Ehtisham S; Department of Paediatric EndocrinologyRoyal Manchester Children's Hospital, Central Manchester Foundation Hospitals NHS Trust, Manchester, UK.
  • Campbell J; Department of Paediatric EndocrinologyRoyal Manchester Children's Hospital, Central Manchester Foundation Hospitals NHS Trust, Manchester, UK.
  • Ainsworth S; Department of Paediatric EndocrinologyRoyal Manchester Children's Hospital, Central Manchester Foundation Hospitals NHS Trust, Manchester, UK.
  • Marshall M; Department of Paediatric EndocrinologyRoyal Manchester Children's Hospital, Central Manchester Foundation Hospitals NHS Trust, Manchester, UK.
  • Bone M; Department of BiochemistryCentral Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
  • Doughty I; Department of General PaediatricsRoyal Manchester Children's Hospital, Central Manchester Foundation Hospitals NHS Trust, Manchester, UK.
  • Clayton PE; Department of General PaediatricsRoyal Manchester Children's Hospital, Central Manchester Foundation Hospitals NHS Trust, Manchester, UK.
Endocr Connect ; 6(4): 225-231, 2017 May.
Article en En | MEDLINE | ID: mdl-28381562
ABSTRACT

BACKGROUND:

Higher 25(OH)D3 levels are associated with lower HbA1c, but there are limited UK interventional trials assessing the effect of cholecalciferol on HbA1c.

AIMS:

(1) To assess the baseline 25(OH)D3 status in a Manchester cohort of children with type 1 diabetes (T1D). (2) To determine the effect of cholecalciferol administration on HbA1c.

METHODS:

Children with T1D attending routine clinic appointments over three months in late winter/early spring had blood samples taken with consent. Participants with a 25(OH)D3 level <50 nmol/L were treated with a one-off cholecalciferol dose of 100,000 (2-10 years) or 160,000 (>10 years) units. HbA1c levels before and after treatment were recorded.

RESULTS:

Vitamin D levels were obtained from 51 children. 35 were Caucasian, 11 South Asian and 5 from other ethnic groups. 42 were vitamin D deficient, but 2 were excluded from the analysis. All South Asian children were vitamin D deficient, with mean 25(OH)D3 of 28 nmol/L. In Caucasians, there was a negative relationship between baseline 25(OH)D3 level and HbA1c (r = -0.484, P < 0.01). In treated participants, there was no significant difference in mean HbA1c at 3 months (t = 1.010, P = 0.328) or at 1 year (t = -1.173, P = 0.248) before and after treatment. One-way ANCOVA, controlling for age, gender, ethnicity, BMI and diabetes duration showed no difference in Δ HbA1c level.

CONCLUSION:

We report important findings at baseline, but in children treated with a stat dose of cholecalciferol, there was no effect on HbA1c. Further studies with larger sample sizes and using maintenance therapy are required.
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