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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Vitamin E and Reduced Alanine Aminotransferase Level

Research synthesisModerate evidenceMixed effect size4 studies · 4 beneficial · 0 neutral · 0 harmful

Across 4 studies, all reported beneficial effects of vitamin E supplementation on reducing alanine aminotransferase (ALT) levels in patients with non-alcoholic fatty liver disease (NAFLD), with 3 reaching statistical significance. The predominant effect sizes were mixed (small to moderate), and effects were typically observed at 8–12 weeks (median study duration 72 days). The most commonly studied dose range was 400–1000 IU per day.

  • Effective dose range: 400–1000 IU/day
  • Studied populations: patients with non-alcoholic fatty liver disease (NAFLD)

Caveats: 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). Evidence base is small (only 4 studies) — conclusions should be considered preliminary. Effect sizes varied from small to moderate across studies, and one meta-analysis (2024) found the effect did not reach statistical significance despite an overall beneficial trend.

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 4 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.
4 of 4 papers
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