Table 1.
Summary of studies evaluating the effects of statin use in patients with NASH/NAFL.
| Authors (Ref) | Study design | Statin | Population health status | Sample size | Main findings |
|---|---|---|---|---|---|
| Athyros et.al. (59) | Randomized trial (post-hoc analysis) |
Atorvastatin vs. simvastatin | Patients with cardiovascular disease | 437 | -Participants treated with statins had improvement in liver tests (p < 0.0001) -Cardiovascular events occurred in 10% of patients with abnormal liver tests who received statin and 30% of patients with abnormal liver tests who did not receive statins (p < 0.0001) |
| Tikkanen et al. (60) | Randomized trial (post-hoc analysis) |
Atorvastatin 80 mg/day vs. simvastatin 20–40mg/day | Coronary heart disease patients with normal and elevated baseline levels of serum alanine aminotransferase | 1,081 | Patients with elevated baseline aminotransferases, major cardiovascular event rates were 11.5% for simvastatin and 6.5% for atorvastatin, indicating a significant risk reduction with intensive statin therapy (HR, 0.556; 95% CI, 0.367–0.842; p = 0.0056) |
| Athyros et al. (40) | Randomized trial (post-hoc analysis) |
Atorvastatin 30 mg/day vs. atorvastatin 20 mg/day. | Patients with metabolic syndrome without diabetes or cardiovascular disease | 326 | The number of events were none for the LDL-C <100 mg/dl group and 3 for the LDL-C <130 mg/dl group |
|
NCT04679376 (active, not recruiting yet) |
Randomized | Atorvastatin 40 mg/day vs. placebo | NASH patients | 70 | Primary objective: change in NASH score |
HR, hazard-ratio; CI, confidence intervals.