Effect of High-Dose Vitamin E on Insulin Resistance and Associated Parameters in Overweight Subjects
- Patrick J. Manning, MMEDSC, FRACP1,
- Wayne H.F. Sutherland, PHD1,
- Robert J. Walker, MD, FRCP1,
- Sheila M. Williams, MSC2,
- Sylvia A. de Jong1,
- Anne R. Ryalls1 and
- Elizabeth A. Berry1
- 1Department of Medical and Surgical Sciences, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand
- 2Department of Preventive and Social Medicine, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand
- Address correspondence and reprint requests to Dr. Patrick J. Manning, Department of Medical and Surgical Sciences, University of Otago, Private bag, Dunedin, New Zealand. E-mail: patrickmanning{at}healthotago.co.nz
Abstract
OBJECTIVE—Markers of oxidative stress and plasma alanine transferase (ALT) levels are increased and circulating antioxidant concentrations are reduced in individuals with insulin resistance. Vitamin E improves glycemic control in people with diabetes. We tested the hypothesis that vitamin E would decrease markers of oxidative stress and plasma ALT levels and improve insulin sensitivity in overweight individuals.
RESEARCH DESIGN AND METHODS—Eighty overweight individuals (BMI >27 kg/m2) were randomly allocated to receive either 800 IU vitamin E per day or a matching placebo for 3 months. The dose of vitamin E was increased to 1,200 IU per day for a further 3 months.
RESULTS—Plasma peroxides decreased by 27% at 3 months and by 29% at 6 months in the group that received vitamin E and were positively correlated with plasma vitamin E concentrations at the 6-month time point. At 3 months, fasting plasma glucose and insulin concentrations were significantly reduced and homeostasis model assessment increased. These changes were not apparent at 6 months. Plasma ALT concentrations declined significantly throughout the study period.
CONCLUSIONS—In conclusion, these findings indicate that vitamin E improves oxidative stress and hepatocellular function. Although insulin resistance also improves, this effect appears transient.
- ALT, alanine transferase
- AST, aspartate aminotransferase
- CRP, C-reactive protein
- FFA, free fatty acid
- GGT, γ-glutamyl transferase
- HOMA, homeostasis model assessment
- IL, interleukin
- ROS, reactive oxygen species
- TNF, tumor necrosis factor
Footnotes
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A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.
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- Accepted June 15, 2004.
- Received April 4, 2004.
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