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Ergocalciferol in New-onset Type 1 Diabetes: A Randomized Controlled Trial
Benjamin Udoka Nwosu1, Sadichchha Parajuli1, Gabrielle Jasmin1
1Division of Pediatric Endocrinology, Department of Pediatrics, University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA.
Vitamin D supplementation with ergocalciferol in type 1 diabetes (T1D) youth reduced inflammation and slowed the rise in HbA1c. This suggests ergocalciferol may protect residual beta-cell function and prolong remission in newly diagnosed T1D.
Area of Science:
- Endocrinology
- Immunology
- Nutritional Science
Background:
- The role of vitamin D in type 1 diabetes (T1D) management is not fully understood.
- Vitamin D possesses anti-inflammatory and immunomodulatory properties.
Purpose of the Study:
- To investigate the impact of ergocalciferol on residual beta-cell function (RBCF) and partial remission (PR) in newly diagnosed T1D youth.
- To test the hypothesis that ergocalciferol supplementation enhances RBCF and extends PR.
Main Methods:
- A 12-month randomized, double-blind, placebo-controlled trial involving 36 youth (10-21 years) with recent T1D diagnosis.
- Participants received either ergocalciferol (50,000 IU weekly then bi-weekly) or a placebo.
- Key metrics included stimulated C-peptide (SCP), HbA1c, and insulin dose-adjusted A1c (IDAA1c).
Main Results:
- Ergocalciferol significantly increased serum 25-hydroxyvitamin D levels and decreased TNF-α concentration.
- No significant differences were observed in SCP or HbA1c between groups.
- However, temporal trends for rising HbA1c and IDAA1c were significantly blunted in the ergocalciferol group.
Conclusions:
- Ergocalciferol supplementation effectively reduced inflammation (TNF-α) and slowed glycemic deterioration (HbA1c, IDAA1c) in newly diagnosed T1D youth.
- These findings suggest a protective effect on residual beta-cell function and partial remission.
- Further research is warranted to confirm these benefits in T1D management.
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