Publication | Open Access
PNPLA3 as a Genetic Determinant of Risk for and Severity of Non-alcoholic Fatty Liver Disease Spectrum
49
Citations
62
References
2016
Year
<b><i>Background and Aims:</i></b><i>Patatin-like phospholipase domain protein 3</i> (<i>PNPLA3</i>) polymorphisms (<i>rs738409</i> C>G) are associated with non-alcoholic fatty liver disease (NAFLD). We performed a systematic review and meta-analysis to examine the association of <i>PNPLA3</i> polymorphisms with the spectrum and severity of this disease. <b><i>Methods:</i></b> Studies evaluating the association between the <i>PNPLA3</i> polymorphism spectrum (fatty liver, steatohepatitis, cirrhosis, and hepatocellular carcinoma) and NAFLD were included. Pooled data are reported as odds ratios (ORs) with 95% confidence intervals. <b><i>Results:</i></b> Of 393 potentially relevant studies, 35 on NAFLD were included in the analysis. Compared to healthy controls, the pooled ORs for <i>rs738409</i> CG and GG compared to CC among patients with non-alcoholic fatty liver (NAFL) were 1.46 (1.16-1.85) and 2.76 (2.30-3.13), and were 1.75 (1.24-2.46) and 4.44 (2.92-6.76) among patients with non-alcoholic steatohepatitis respectively. The respective ORs for CG and GG compared to the CC genotype were 2.35 (0.90-6.13) and 5.05 (1.47-17.29) when comparing non-alcoholic hepatocellular carcinoma to NAFL patients. Among the NAFLD patients, the ORs for G allele frequency when comparing steatosis grade 2-3 to grade 0-1 NAFL, when comparing the NAFLD activity score of ≥ 4 to score ≤ 3, when comparing NASH to NAFLD, when comparing the presence of lobular inflammation to absence, and when comparing the presence of hepatocyte ballooning to absence were 2.33 (1.43-3.80), 1.80 (1.36-2.37), 1.66 (1.42-1.94), 1.58 (1.19-2.10), and 2.63 (1.87-3.69) respectively. Subgroup analysis based on ethnicity showed similar results. <b><i>Conclusions:</i></b><i>PNPLA3</i> polymorphisms have strong association with the risk for and severity of NAFLDs. <i>PNPLA3</i> polymorphism plays an evolving role in diagnosis and treatment decisions in patients with NAFLD.
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