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The effects of vitamin D supplementation on metabolic profiles and liver function in patients with non-alcoholic fatty liver disease: A systematic review and meta-analysis of randomized controlled trials.

Diabetes & metabolic syndrome
December 1, 2017
Reza Tabrizi et al. (8 authors)
Journal ArticleMeta-AnalysisReviewSystematic ReviewHuman Study
Study Details

Study Goal

The researchers aimed to determine the effect of vitamin D supplementation on metabolic profiles, including alanine aminotransferase (ALT) levels, in patients with non-alcoholic fatty liver disease (NAFLD).

Results Summary

The study found that vitamin D supplementation had no significant effect on ALT levels (SMD -0.66; 95% CI, -1.43, 0.11) or other metabolic markers in NAFLD patients.

Population

Patients with non-alcoholic fatty liver disease (NAFLD) (227 patients and 225 controls).

Effective Dosage

Not specified in the abstract.

Duration

Not specified in the abstract.

Interactions

None mentioned.

Extracted Claims (8)
InterventionDirectionEndpointPopulationDosageImpactClaim #
vitamin D administration
no change
fasting plasma glucose (FPG)
patients with non-alcoholic fatty liver disease (NAFLD)
SMD -0.23; 95% CI, -0.88, 0.42
had no beneficial effect
#1
vitamin D administration
no change
insulin
patients with non-alcoholic fatty liver disease (NAFLD)
SMD -1.09; 95% CI, -2.70,0.52
had no beneficial effect
#2
vitamin D administration
no change
homeostasis model assessment of insulin resistance (HOMA-IR)
patients with non-alcoholic fatty liver disease (NAFLD)
SMD -1.89; 95% CI, -3.88,0.09
had no beneficial effect
#3
vitamin D supplementation
no change
triglycerides
patients with non-alcoholic fatty liver disease (NAFLD)
SMD -0.36; 95% CI, -1.77, 1.04
had no effect
#4
vitamin D supplementation
no change
total-cholesterol
patients with non-alcoholic fatty liver disease (NAFLD)
SMD -0.46; 95% CI: -1.3, 0.39
had no effect
#5
vitamin D supplementation
no change
aspartate transaminase (AST)
patients with non-alcoholic fatty liver disease (NAFLD)
SMD -0.53; 95% CI, -1.11, 0.05
had no effect
#6
vitamin D supplementation
no change
alanine aminotransferase (ALT)
patients with non-alcoholic fatty liver disease (NAFLD)
SMD -0.66; 95% CI, -1.43,0.11
had no effect
#7
vitamin D supplementation
no change
body mass index (BMI)
patients with non-alcoholic fatty liver disease (NAFLD)
SMD -0.25; 95% CI, -0.76,0.27
had no effect
#8
Abstract

BACKGROUND: A systematic review and meta-analysis of randomized controlled trials (RCTs) was conducted to summarize the evidence on the effect of vitamin D supplementation on metabolic profiles in patients with non-alcoholic fatty liver disease (NAFLD). METHODS: We systematically searched PubMed, EMBASE and five other databases to identify all RCTs investigating the association between vitamin D and NAFLD up until 5 October 2016. Seven RCTs with 452 participants (227 patients and 225 controls) were included in the meta-analysis. RESULTS: The results showed that vitamin D administration had no beneficial effect on fasting plasma glucose (FPG) (standardized mean difference [SMD]-0.23; 95% confidence interval [CI], -0.88, 0.42), insulin (SMD -1.09; 95% CI, -2.70,0.52) and homeostasis model assessment of insulin resistance (HOMA-IR) (SMD -1.89; 95% CI, -3.88,0.09). Vitamin D supplementation also had no effect on lipid profiles including triglycerides (SMD -0.36; 95% CI, -1.77, 1.04), and total-cholesterol (SMD -0.46; 95% CI: -1.3, 0.39), as well as on aspartate transaminase (AST) (SMD -0.53; 95% CI, -1.11, 0.05), alanine aminotransferase (ALT) (SMD -0.66; 95% CI, -1.43,0.11), and body mass index (BMI) (SMD -0.25; 95% CI, -0.76,0.27). CONCLUSIONS: Vitamin D supplementation had no effect on FPG, insulin, HOMA-IR, triglycerides, total-, LDL-cholesterol, AST, ALT, and BMI.

Medical Subject Headings (MeSH)
Blood GlucoseDietary SupplementsHumansLipidsLiverNon-alcoholic Fatty Liver DiseaseVitamin D
Study Links
Quality Scores
SafetyNot Assessed
Efficacy20/10
Quality75/10
Citation Metrics
Total Citations44
Citations/Year5.5
Relative Citation Ratio2.13
NIH Percentile76.4%
Research Impact Scores
APT Score0.75
Weight Score2.02
Normalized Score0.43
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