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Effect of dexamethasone therapy on serum vitamin E concentrations in premature infants with bronchopulmonary
Sanjiv B Amin1, Nirupama Laroia, Robert A Sinkin
1Department of Pediatrics, Division of Neonatology, Children's Hospital at Strong University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Insights
Dexamethasone therapy significantly increases serum vitamin E levels in premature infants with bronchopulmonary dysplasia. This rise in vitamin E is linked to increased triglycerides and occurs regardless of vitamin E intake.
Area of Science:
- Neonatal Medicine
- Pharmacology
- Nutritional Science
Background:
- Bronchopulmonary dysplasia (BPD) is a chronic lung disease affecting premature infants.
- Dexamethasone is a corticosteroid used to treat BPD, but its metabolic effects are not fully understood.
- Vitamin E is a crucial antioxidant with potential roles in lung health.
Purpose of the Study:
- To investigate the impact of dexamethasone therapy on serum vitamin E concentrations in premature infants diagnosed with BPD.
- To explore the relationship between dexamethasone, vitamin E, and lipid metabolism in this vulnerable population.
Main Methods:
- Prospective study involving 10 premature infants (24-29 weeks gestational age) receiving dexamethasone therapy.
- Serum vitamin E and triglyceride levels were measured at baseline and during dexamethasone treatment in 8 infants.
- Vitamin E intake was assessed via chart review.
Main Results:
- Serum vitamin E concentrations significantly increased during dexamethasone therapy (P=0.01).
- Six of eight infants exhibited pharmacological levels of serum vitamin E (> or =3 mg/dl) post-treatment.
- Increased serum vitamin E correlated significantly with increased serum triglyceride levels (Spearman's rho=0.92).
- Vitamin E intake did not differ significantly between baseline and treatment periods.
Conclusions:
- Dexamethasone therapy in premature infants with BPD leads to a significant elevation in serum vitamin E concentrations.
- The observed increase in vitamin E reaches pharmacological levels and is independent of dietary vitamin E intake.
- The findings suggest a potential interaction between dexamethasone and vitamin E metabolism, possibly linked to altered lipid profiles.
Objective:
To investigate the effect of dexamethasone therapy on serum vitamin E concentrations in premature infants with bronchopulmonary dysplasia.
Study Design:
A total of 10, 24 to 29 weeks' gestational age, infants enrolled in a prospective study designed to evaluate the effect of dexamethasone on lipid intolerance were eligible for the study. Eight of these 10 infants had serum vitamin E concentrations measured simultaneously with serum triglyceride concentrations before the start of dexamethasone therapy (baseline) and within 5 days of the initiation of dexamethasone therapy. Charts were reviewed for vitamin E intake at baseline and on dexamethasone therapy for each of these eight infants.
Results:
All eight infants had physiological serum vitamin E concentrations (1 to 3 mg/dl) at baseline, while six of eight infants had pharmacological serum vitamin E concentrations (> or =3 mg/dl) on dexamethasone therapy. All infants with an increase in serum vitamin E concentration also had a simultaneous increase in serum triglyceride concentrations with a significant correlation between vitamin E and triglyceride concentrations (Spearman's rho=0.92). There was a significant difference in mean serum vitamin E concentration between baseline and post-dexamethasone therapy (P=0.01, Wilcoxon's signed-rank test). There was no significant difference in vitamin E intake between baseline and post-dexamethasone therapy.
Conclusion:
Dexamethasone therapy in premature infants induces significant increase in serum vitamin E concentrations to pharmacological levels independent of vitamin E intake.
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