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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Vitamin E and Reduced Aspartate Aminotransferase Level

Research synthesisModerate evidenceSmall effect5 studies · 3 beneficial · 2 neutral · 0 harmful

Across 5 studies, 3 reported beneficial small-to-moderate effects of vitamin E on reducing aspartate aminotransferase (AST) levels, while 2 found neutral effects. The predominant effect size is small. Evidence primarily comes from patients with NAFLD/MASLD, with doses ranging from 300 to 1000 IU/day. Median study duration was 72 days, suggesting effects typically observed at 8–12 weeks.

  • Effective dose range: 300–1000 IU/day
  • Studied populations: patients with NAFLD/NASH/MASLD

Caveats: Many of the included studies did not reach statistical significance — effect may be smaller than the predominant direction suggests. Available evidence is overwhelmingly positive — clinical literature in this area is subject to publication bias (null-result studies are less likely to be published or indexed).

Generated Jun 11, 2026
Doses used in studies
  • IU/day: 298–1,000 (median 524.5, IQR 323.5850) 2 studies
  • mg/day: 300–800 (median 550, IQR 300800) 1 study
Time to effect
Median: 10.3 weeks · IQR 9.4 weeks11.1 weeks · Range 8.6 weeks2.8 months — Reported in 2 of 5 studies
Safety in these studies
  • all-cause mortalityNo significant differenceSerious adverse eventRR 3.45, 95% CI 0.57 to 20.86

    The effects of vitamin E versus placebo or no intervention on all-cause mortality (risk ratio (RR) 3.45, 95% confidence interval (CI) 0.57 to 20.86; 3 trials, 351 participants; very low certainty evidence) and serious adverse events (RR 1.91, 95% CI 0.30 to 12.01; 2 trials, 283 participants; very low certainty evidence) are very uncertain.

    from: Vitamin E for people with non-alcoholic fatty liver disease.
  • serious adverse eventsNo significant differenceSerious adverse eventRR 1.91, 95% CI 0.30 to 12.01

    The effects of vitamin E versus placebo or no intervention on all-cause mortality (risk ratio (RR) 3.45, 95% confidence interval (CI) 0.57 to 20.86; 3 trials, 351 participants; very low certainty evidence) and serious adverse events (RR 1.91, 95% CI 0.30 to 12.01; 2 trials, 283 participants; very low certainty evidence) are very uncertain.

    from: Vitamin E for people with non-alcoholic fatty liver disease.
  • Overall tolerabilityReported

    The effects of vitamin E versus placebo or no intervention on physical health-related quality of life ... and non-serious adverse events (RR 0.86, 95% CI 0.64 to 1.17; 2 trials, 283 participants; very low certainty evidence) are also very uncertain.

    from: Vitamin E for people with non-alcoholic fatty liver disease.
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