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Figure 1

Study selection flow diagram
Study selection flow diagram

Figure 2

Forest plot displaying the effect of statin on Std diff of steatosis grading. CI, confidence interval; Std diff, standardized mean difference
Forest plot displaying the effect of statin on Std diff of steatosis grading. CI, confidence interval; Std diff, standardized mean difference

Figure 3

Forest plot displaying the effect of statin on Std diff of NAFLD activity score (NAS). CI, confidence interval; NAFLD, non-alcoholic fatty liver disease; NAS, non-alcoholic fatty liver disease activity score; Std diff, standardized mean difference
Forest plot displaying the effect of statin on Std diff of NAFLD activity score (NAS). CI, confidence interval; NAFLD, non-alcoholic fatty liver disease; NAS, non-alcoholic fatty liver disease activity score; Std diff, standardized mean difference

Figure 4

Forest plot displaying the effect of statin on Std diff of fibrosis stage. CI, confidence interval; Std diff, standardized mean difference
Forest plot displaying the effect of statin on Std diff of fibrosis stage. CI, confidence interval; Std diff, standardized mean difference

Risk of bias for the randomized controlled trial by Nelson et al. [18]

GradeBias
Random sequence generation (selection bias)
Allocation concealment (selection bias)
Blinding of participants and personnel (performance bias)
Blinding of outcome assessment (detection bias)
Incomplete outcome data (attrition bias)
Selective reporting (reporting bias)

Outcomes and main findings of the studies included in the meta-analysis

Author (year)OutcomesMain findings
% of steatosisSteatosis gradingNASNecroinflammatory activity gradeFibrosis stageTotal cholesterolTriglycerideHDLLDLALTAST
Nelson et al. (2009) [18]YesNoNoYesYesYesYesNoYesYesYes- 26% reduction in LDL between simvastatin vs placebo
- No statistically significant improvement in ALT, AST, hepatic steatosis, necroinflammatory activity, or stage of fibrosis within or between groups
Ekstedt et al. (2007) [13]YesNoNoNoYesYesYesNoNoYesYes- Significant reduction in quantitative steatosis in the statin cohort between baseline and follow-up
- AST/ALT did not differ significantly between the two cohorts
Hyogo et al. (2011) [14]NoYesYesYesYesYesYesYesYesYesYes- Significant decrease in ALT and lipid profiles
- NAS tended to be decreased but statistical significance was not shown
- Fibrosis stage did not change significantly
Nakahara et al. (2012) [15]NoYesYesNoYesYesYesYesYesYesYes- Mean AST/ALT did not significantly change during the treatment
- NAS and fibrotic stage tended to decrease after the treatment but statistical significance was not shown
Hyogo et al. (2012) [16]NoNoYesNoNoYesYesYesYesYesYes- Significant decrease in AST and ALT
- Significant improvement in NAS
Kargiotis et al. (2015) [17]NoYesYesNoNoYesYesYesYesNoNo- Complete resolution of NASH in 19 of 20 patients
- AST, ALT, and lipid profiles were normalized by the 3rd month of treatment

Summary effects of statins on liver steatosis and fibrosis parameters

OutcomesStudies, nPatients, nStandardized mean changePAssessment of heterogeneityI2 index, % Q-test, P
% of steatosis227–0.580 (–1.599, 0.439)0.26593<0.001
Steatosis grading342–2.580 (–4.623, –0.536)0.01398<0.001
NAFLD activity score484–1.488 (–2.506, –0.471)0.00496<0.001
Necroinflammatory activity grade223–0.112 (–0.372, 0.148)0.39800.454
Fibrosis stage4490.156 (–0.553, 0.865)0.66792<0.001
Total cholesterol6111–1.540 (–2.221, –0.859)<0.00193<0.001
Triglyceride6111–0.764 (–1.334, –0.195)0.00994<0.001
High-density lipoprotein4840.423 (–0.070, 0.917)0.09389<0.001
Low-density lipoprotein594–1.865 (–2.416, –1.313)<0.00183<0.001
Alanine transaminase591–0.511 (–0.650, –0.373)<0.00100.680
Aspartate aminotransferase591–0.462 (–0.599, –0.325)<0.00100.594

Characteristics of the studies included in the meta-analysis

AuthorYear [ref]CountryStudy designPatients, n

Number of patients in statin treatment arm,

Type of statin (mg/dL)Follow-up time (year)Statin duration (year)Study quality

Quality assessment using Cochrane Collaboration’s tool for assessing risk of bias for RCT and Cochrane assessment of bias for non-randomized studies tool (ROBINS-I).

Nelson et al2009 [18]USARCT10

data from the statin arm.

Simvastatin (40)11Low

Risk of bias legend for RCT illustrated in Table 4

Ekstedt et al2007 [13]SwedenRetrospective17NA10.3–16.31–15.9Ser

Risk of bias legend for nonrandomized studies illustrated in Table 5.

cohort
Hyogo et al2011 [14]JapanProspective13Pitavastatin (2)11Mod

Risk of bias legend for nonrandomized studies illustrated in Table 5.

cohort
Nakahara et al2012 [15]JapanProspective9Rosuvastatin (2.5)22Mod

Risk of bias legend for nonrandomized studies illustrated in Table 5.

cohort
Hyogo et al2012 [16]JapanProspective42Atorvastatin (10)11Mod

Risk of bias legend for nonrandomized studies illustrated in Table 5.

cohort
Kargiotis et al2015 [17]GreeceProspective20Rosuvastatin (10)11Mod

Risk of bias legend for nonrandomized studies illustrated in Table 5.

cohort

Risk of bias assessment for nonrandomized studies

DomainEkstedt et al. [13]Hyogo et al. [14]Nakahara et al. [15]Hyogo et al. [16]Kargiotis et al. [17]
ConfoundingModerateModerateModerateModerateModerate
SelectionSeriousLowLowLowLow
Measurement of interventionsSeriousLowLowLowLow
PerformanceLowLowLowLowLow
Missing dataLowLowLowLowLow
Measurement of outcomesLowLowLowLowLow
ReportingLowLowLowLowLow
OverallSeriousModerateModerateModerateModerate
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