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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Vitamin E and Reduced Alanine Aminotransferase Level

Research synthesisLow evidenceSmall effect3 studies · 3 beneficial · 0 neutral · 0 harmful

Across 3 studies, all reported beneficial effects of vitamin E on reducing alanine aminotransferase (ALT) levels, with effect sizes ranging from small to moderate. Two of three studies found statistically significant reductions. The evidence primarily comes from clinical populations with non-alcoholic fatty liver disease (NAFLD) or metabolic dysfunction-associated steatohepatitis (MASH), with a median study duration of 72 days (approximately 10 weeks). The most-studied dose range is 298–1000 IU/day.

  • Effective dose range: 298–1000 IU/day
  • Studied populations: people with non-alcoholic fatty liver disease (NAFLD) and metabolic dysfunction-associated steatohepatitis (MASH)

Caveats: Evidence base is small (only 3 studies) — conclusions should be considered preliminary. 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). The highest-quality evidence (moderate certainty meta-analysis) reported a small beneficial effect that was not statistically significant when analyzed independently, suggesting the true effect may be small.

Generated May 15, 2026
Doses used in studies
  • IU/day: 298–1,000 (median 649, IQR 2981,000) 1 study
  • 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 3 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.
3 of 3 papers
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