Xia Li and Lan Liao contributed equally to this work.
Research Article
Protective effects of 1-α-hydroxyvitamin D3 on residual β-cell function in patients with adult-onset latent autoimmune diabetes (LADA)
Article first published online: 1 JUN 2009
DOI: 10.1002/dmrr.977
Copyright © 2009 John Wiley & Sons, Ltd.
Additional Information
How to Cite
Li, X., Liao, L., Yan, X., Huang, G., Lin, J., Lei, M., Wang, X. and Zhou, Z. (2009), Protective effects of 1-α-hydroxyvitamin D3 on residual β-cell function in patients with adult-onset latent autoimmune diabetes (LADA). Diabetes/Metabolism Research and Reviews, 25: 411–416. doi: 10.1002/dmrr.977
Publication History
- Issue published online: 29 JUN 2009
- Article first published online: 1 JUN 2009
- Manuscript Accepted: 23 APR 2009
- Manuscript Revised: 27 MAR 2009
- Manuscript Received: 22 OCT 2008
Funded by
- National Natural Science Foundation of China. Grant Number: 30600298
- Hunan Natural Science Foundation. Grant Numbers: 06JJ20086, 08JJ4007
- National 973. Grant Number: 2006CB503901
- Abstract
- Article
- References
- Cited By
Keywords:
- latent autoimmune diabetes in adults;
- vitamin D;
- β-cell function;
- insulin;
- intervention
Abstract
Background
Previous in vitro and in vivo studies have demonstrated that vitamin D could prevent pancreatic β-cell destruction and reduce the incidence of autoimmune diabetes. In children with type 1 diabetes, vitamin D treatment produces moderate protective effects on residual β-cell function and has proven to be safe. Therefore, we hypothesized that vitamin D might have protective effects on β-cell function in patients with latent autoimmune diabetes in adults (LADA), a form of slowly progressive autoimmune type 1 diabetes.
Methods
Thirty-five patients with LADA were randomly assigned to receive subcutaneous insulin alone (n = 18) or insulin plus 1-α-hydroxyvitamin D3 (1-α(OH)D3; 0.5 µg per day) (n = 17) for 1 year. Plasma C-peptide levels in fasting state (FCP) and 2 h after 75-g glucose load (PCP) were measured every 6 months with radioimmunoassay.
Results
Both FCP and PCP levels stayed steady in the insulin plus 1-α(OH)D3 group, while FCP decreased in insulin-alone group (P = 0.006) during the 12-month intervention. Seventy percent of patients treated with 1-α(OH)D3 maintained or increased their FCP concentrations after 1 year of treatment, while only 22% of patients treated with insulin alone maintained stable FCP levels (P < 0.01). Further analysis on LADA subgroups with different durations of diabetes demonstrated that islet β-cell function was better preserved (as reflected by significantly higher FCP and PCP levels) in the 1-α(OH)D3 plus insulin group only in patients with diabetes duration no longer than 1 year. No severe side effects were observed in any group.
Conclusion
Our data suggest that 1-alpha(OH)D3 plus insulin therapy can preserve pancreatic β-cell function in patients with LADA. Copyright © 2009 John Wiley & Sons, Ltd.

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