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[Protective effect of vitamin A on residual pancreatic β cell function in children with type 1 diabetes mellitus]
Yong-Xing Chen1, Qiong Chen, Ying-Xian Zhang
1Department of Endocrinology and Inherited Metabolism, Children's Hospital Affiliated to Zhengzhou University/Henan Children's Hospital/Zhengzhou Children's Hospital, Zhengzhou 450000, China. haiyanwei2009@163.com.
Insights
Vitamin A supplementation may preserve pancreatic beta cell function in children with type 1 diabetes mellitus (T1DM). This intervention reduced interleukin-17 (IL-17) levels and improved insulin sensitivity.
Area of Science:
- Endocrinology
- Immunology
- Pediatrics
Background:
- Type 1 diabetes mellitus (T1DM) is an autoimmune disease characterized by the destruction of pancreatic beta cells.
- Residual beta cell function is crucial for glycemic control and long-term outcomes in T1DM.
- Interleukin-17 (IL-17) is implicated in autoimmune inflammation and beta cell destruction.
Purpose of the Study:
- To investigate the protective effects of vitamin A on residual pancreatic beta cell function in children with T1DM.
- To explore the potential mechanism involving IL-17 modulation.
Main Methods:
- A randomized controlled trial involving 46 children with T1DM and 25 healthy controls.
- Intervention group received vitamin A (1500-2000 IU/day) alongside insulin therapy.
- Measurements included glycosylated hemoglobin (HbA1C), stimulated C-peptide, vitamin A, and IL-17 levels before and after 3 months.
Main Results:
- Children with T1DM had lower vitamin A and higher IL-17 levels compared to controls.
- Vitamin A intervention significantly reduced IL-17 levels and insulin requirements.
- The intervention group showed significantly higher stimulated C-peptide levels post-treatment.
Conclusions:
- Vitamin A supplementation appears to protect residual pancreatic beta cell function in T1DM.
- The protective effect may be mediated by the modulation of IL-17 secretion.
- Vitamin A is a potential therapeutic adjunct for managing T1DM in children.
Objective:
To study the protective effect of vitamin A on residual pancreatic β cell function in children with type 1 diabetes mellitus (T1DM) and its mechanism.
Methods:
A total of 46 children with T1DM (with a course of disease of 0.5-1 year) were randomly divided into an intervention group and a non-intervention group (n=23 each). The children in both groups were given insulin treatment, and those in the intervention group were also given vitamin A at a daily dose of 1 500-2 000 IU. A total of 25 healthy children were enrolled as the control group. The daily dose of insulin was calculated for the children with T1DM, and the serum levels of glycosylated hemoglobin (HbA1C), stimulated C-peptide, vitamin A, and interleukin-17 (IL-17) were measured before intervention and 3 months after intervention.
Results:
Before vitamin A intervention, the intervention group and the non-intervention group had a significantly lower serum level of vitamin A and a significantly higher level of IL-17 than the control group (P<0.01). After 3 months of intervention, the intervention group had significantly lower serum IL-17 level and insulin dose and a significantly higher level of stimulated C-peptide than the non-intervention group (P<0.05).
Conclusions:
Vitamin A may protect residual pancreatic β cell function, possibly by improving the abnormal secretion of IL-17 in children with T1DM.
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