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Meta-Analysis
. 2018 Oct;48(7):696-703.
doi: 10.1111/apt.14937. Epub 2018 Aug 22.

Systematic review with meta-analysis: risk of hepatocellular carcinoma in non-alcoholic steatohepatitis without cirrhosis compared to other liver diseases

Affiliations
Meta-Analysis

Systematic review with meta-analysis: risk of hepatocellular carcinoma in non-alcoholic steatohepatitis without cirrhosis compared to other liver diseases

Jonathan G Stine et al. Aliment Pharmacol Ther. 2018 Oct.

Abstract

Background: Given the lack of long-term prospective studies, it is challenging for clinicians to make informed decisions about screening and treatment decisions regarding the risk of hepatocellular carcinoma (HCC) in patients with non-alcoholic steatohepatitis (NASH) who do not have cirrhosis.

Aim: To characterise the pooled risk of HCC in the non-cirrhosis population.

Methods: Published studies were identified through April 2016 in MEDLINE, Scopus, Science Citation Index, AMED and the Cochrane Library. Two independent reviewers screened citations and extracted data. Random effect odds ratios (OR) were calculated to obtain aggregate estimates of effect size between NASH and non-NASH groups. Between-study variability and heterogeneity were assessed.

Results: Nineteen studies with 168 571 participants were included. Eighty-six per cent of included subjects had cirrhosis. The prevalence of HCC in non-cirrhotic NASH was 38.0%; among other aetiologies in non-cirrhotics, it was 14.2% (P < 0.001). Non-cirrhotic NASH subjects were at greater odds of developing HCC than non-cirrhotic subjects of other aetiologies (OR 2.61, 95% CI 1.27-5.35, P = 0.009). When examining all NASH subjects either with or without cirrhosis, those with NASH as the underlying liver disease did not have a significantly increased risk of HCC (OR 1.43, 95% CI 0.77-2.65, P = 0.250).

Conclusions: In non-cirrhotic subjects, those with NASH have a higher risk of HCC compared to other aetiologies of liver disease. Further study investigating the risk factors of HCC among non-cirrhotic NASH patients is needed.

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Figures

FIGURE 1
FIGURE 1
PRISMA diagram for search scheme for HCC risk in NASH
FIGURE 2
FIGURE 2
A, Pooled measure of effects for NASH and HCC in all patients (either with or without cirrhosis). There was a trend towards significance with increased risk of HCC when comparing NASH patients to all other aetiologies of liver disease, however, this was not statistically significant. B, Pooled measure of effects of NASH and HCC in patients without cirrhosis. The overall pooled estimate from the seven studies indicates that patients with NASH have a 261% increased risk of HCC when compared to all other aetiologies of liver disease

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