Endpoint
Alanine aminotransferase
CAT:outcome/alanine-aminotransferasereported in U/L
Method
Serum alanine aminotransferase catalytic activity by clinical enzymatic assay. Whether the reagent was supplemented with pyridoxal phosphate is recorded on the edge where stated, since it shifts measured activity.
The method is part of the endpoint identity. Studies measuring the same quantity by a different method are held as separate endpoints.
Notes
Aspartate aminotransferase is the near-miss: same liver panel, same unit, same direction of benefit, adjacent columns. The distinction is tissue specificity — this enzyme is hepatocyte-specific while AST is also released by skeletal muscle and erythrocytes — and it is not academic: in PMID 41515249 this fell significantly while AST and gamma-glutamyl transferase did not. Merging them makes a liver-specific effect look like a null. Also distinct from CAT:outcome/creatine-kinase, another serum enzyme activity in U/L that indexes muscle damage rather than liver injury, and SIGN INVERSION against serum albumin on the same panel, which improves by RISING.
Findings
3 findings from 2 compounds, strongest first.
curcumin — decreases
LikelyGrade B, Likely. Human evidence, limited replication or design limits.Findingreplicated ×1“The overall pooling indicated that curcumin supplementation was significantly associated with reduced ALT [MD (95% CI) of −5.61 (−9.37, −1.85) units/L] with moderate heterogeneity observed (I2 = 64.3%).”
Quoted verbatim from An updated meta-analysis of effects of curcumin on metabolic dysfunction-associated fatty liver disease based on available evidence from Iran and Thailand.. - Study
- meta-analysis
- Dose
- 80–3000 mg/day pooled across bioavailability-enhanced forms (80–1000 mg/day), curcumin extracts (1500 mg/day) and turmeric powder (2000–3000 mg/day)
- Population
- Adults with MAFLD (NAFLD/NASH); overall pooling of 14 RCTs, all curcumin forms; liver enzymes were a primary outcome of interest
Effect -5.61 mean difference, 95% CI -9.37 to -1.85
curcumin — decreases
LikelyGrade B, Likely. Human evidence, limited replication or design limits.Findingreplicated ×1“The results showed that curcumin reduced ALT compared with placebo [SMD = -0.55, 95% CI (-1.01, -0.09), P = 0.02].”
Quoted verbatim from Efficacy and safety of dietary polyphenol supplementation in the treatment of non-alcoholic fatty liver disease: A systematic review and meta-analysis.. - Study
- meta-analysis
- Participants
- 639
- Population
- adults with non-alcoholic fatty liver disease
Effect -0.55 standardised mean difference, 95% CI -1.01 to -0.09
Efficacy and safety of dietary polyphenol supplementation in the treatment of non-alcoholic fatty liver disease: A systematic review and meta-analysis.2022PMID:36159792
berberine — decreases
PreliminaryGrade D, Preliminary. Non-human or in vitro only.Finding“However, oral administration of BBR not only reversed hepatocyte necrosis, but also decreased the elevated levels of TBA, ALP, TBIL, DBIL, ALT, and AST ( Supplementary Fig. 1A, 1B).”
Quoted verbatim from Gut microbiota-mediated berberine metabolism ameliorates cholestatic liver disease by suppressing 5-hydroxytryptamine production.. - Study
- animal · not in humans
- Duration
- 7 days
- Population
- C57BL/6J mice with bile duct ligation-induced cholestatic liver injury; serum ALT by automated biochemical analyser
Gut microbiota-mediated berberine metabolism ameliorates cholestatic liver disease by suppressing 5-hydroxytryptamine production.2026PMID:41087029