Effects of metabolic control on vitamin E nutritional status in children with type 1 diabetes mellitus

Clin Nutr. 2003 Feb;22(1):81-6. doi: 10.1054/clnu.2002.0596.

Abstract

Objective: To evaluate the effects of the metabolic control of the insulin-dependent diabetes mellitus (IDDM) on the nutritional status of vitamin E.

Methods: A total of 47 children with IDDM and a mean age of 11.91+/-1.60 (mean+/-SD) years were studied, matched for age and sex with 16 healthy children (11.75+/-1.83 years). Following the American and British Associations for IDDM, we used a classification of "good", "moderate" or "poor" control of the illness: (a) good control [glycosilated haemoglobin (HbAlc) < or =7%]; (b) moderate control (7%< HbAlc < or =8%); and (c) poor control (HbAlc>8%). Serum concentrations of total cholesterol (CHOL), triglycerides (TG), high-density lipoproteins-cholesterol (HDLc), very low- and low-density lipoproteins cholesterol (VLDLc and LDLc), plasma and erythrocyte vitamin E (Vit Ep and Vit Ee) and plasma vitamin A (Vit Ap) were measured in all children.

Results: The children with "poor" metabolic control of the illness presented significantly higher plasma concentrations of CHOL, LDLc, VLDLc, LDLc/HDLc, (VLDL+LDL)c/HDLc, TG and Vit Ep; higher indices Vit Ep/Vit Ee and Vit Ep/Vit Ap relative to those with a "good" control of the illness. Direct-linear correlations were found between Vit Ep and the percentage of HbAlc and with the markers of atherogenic risk in the IDDM children.

Conclusion: There is a significant rise in Vit Ep concentrations as metabolic control of the illness worsens, whereas Vit Ee remained unchanged. These results suggest that vitamin E maintains its nutritional status despite a poor control of the IDDM during childhood.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Analysis of Variance
  • Biomarkers
  • Child
  • Cholesterol / blood
  • Diabetes Mellitus, Type 1 / metabolism*
  • Female
  • Glycated Hemoglobin / analysis
  • Humans
  • Lipoproteins / blood
  • Male
  • Nutritional Status / physiology*
  • Risk Factors
  • Triglycerides / blood
  • Vitamin A / blood
  • Vitamin E / blood*

Substances

  • Biomarkers
  • Glycated Hemoglobin A
  • Lipoproteins
  • Triglycerides
  • Vitamin A
  • Vitamin E
  • Cholesterol