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Effect of nicotinamide on newly diagnosed type 1 diabetic children
Madeeha Kamal1, Abdul-Jabbar Al Abbasy, Ahood Al Muslemani
1Department of Pediatrics, Salmaniya Medical Complex, Manama, Bahrain.
Insights
Low-dose nicotinamide (NA) therapy in children with new-onset type 1 diabetes reduced insulin needs and extended the remission (honeymoon) period. This suggests NA may help manage pediatric type 1 diabetes.
Area of Science:
- Endocrinology
- Metabolic Disorders
- Pediatric Diabetes Management
Background:
- Type 1 diabetes (T1D) is an autoimmune disease characterized by pancreatic beta-cell destruction.
- The 'honeymoon period' in T1D is a temporary phase of reduced insulin needs post-diagnosis.
- Maintaining beta-cell function is crucial for long-term T1D management.
Purpose of the Study:
- To investigate the efficacy of early low-dose nicotinamide (NA) therapy in pediatric patients with newly diagnosed type 1 diabetes.
- To determine if NA treatment can prolong the remission period and decrease insulin requirements.
- To assess the impact of NA on glycemic control in children with T1D.
Main Methods:
- A cohort of 66 pediatric patients with newly diagnosed T1D received nicotinamide (1-2 mg/kg/day) within 24 hours of diagnosis.
- Patients were followed for 24 months, with insulin dosage per kg bodyweight recorded at 3-month intervals.
- Results were compared to a control group (n=37) diagnosed between 1995-1997 who did not receive NA.
Main Results:
- No significant differences in baseline characteristics (age, weight, insulin dose, glucose levels) were observed between the NA and control groups.
- The NA group consistently demonstrated lower insulin requirements compared to the control group at all 3-month intervals up to 2 years post-diagnosis.
- This indicates a potential benefit of NA in reducing exogenous insulin needs.
Conclusions:
- Early administration of low-dose oral nicotinamide may be beneficial in managing pediatric type 1 diabetes.
- NA therapy appears to reduce insulin requirements and potentially prolong the honeymoon period in children with newly diagnosed T1D.
- Further research is warranted to confirm these findings and explore optimal NA dosing strategies.
Aim:
To determine whether a low dose of nicotinamide (NA) therapy for pediatric patients with type 1 diabetes, initiated within the first 24 h of diagnosis, prolongs the honeymoon period and lowers their insulin requirements.
Methods:
All children (n=66) with newly diagnosed type 1 diabetes admitted to Salmaniya Medical Complex between 1998 and 2000, received NA 1-2 mg/kg per day, in addition to sc insulin bid. The patients were followed for 24 months (NA group). Findings in this group were compared with records from a similarly diagnosed control group (n=37), who were admitted to the same hospital between 1995 and 1997 and did not receive NA treatment. The insulin dose per kg bodyweight required at baseline and at 3-monthly intervals up to 2 years after diagnosis was determined.
Results:
At baseline, the two groups did not differ with respect to age, ethnic background, weight, insulin dose per kg bodyweight or glucose levels on admission. However, NA group had lower insulin requirements than control group at each 3-month interval up to 2 years after diagnosis.
Conclusion:
Our study results suggest that even low doses of oral NA given to children with newly diagnosed type 1 diabetes may reduce insulin requirements and prolong the honeymoon period.
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