eISSN: 2449-8238
ISSN: 2392-1099
Clinical and Experimental Hepatology
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2/2019
vol. 5
 
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abstract:
Original paper

A systematic review and meta-analysis of evaluation of serum interleukin 8 levels in hepatocellular carcinoma

Ebrahim Shakiba
1
,
Masoud Sadeghi
2, 3
,
Mohammad Shakiba
3

1.
Department of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran
2.
Medical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran
3.
Students Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran
Clin Exp HEPATOL 2019; 5, 2: 123–128
Online publish date: 2019/05/08
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Aim of the study
To estimate serum interleukin 8 (IL-8) level in patients with hepatocellular carcinoma (HCC) compared to controls and patients with chronic hepatitis (CH) and liver cirrhosis (LC).

Material and methods
Three databases, i.e. PubMed, Web of Science, and Scopus, were searched up to November 2017 without language restriction. The mean difference (MD) and 95% confidence interval (CI) were used by a random-effects analysis in RevMan version 5.3, and sensitivity analysis was performed as the secondary analysis.

Results
Out of 239 studies found, 10 studies recruiting 659 HCC patients, 237 controls, 357 patients with LC, and 48 patients with CH were included and analyzed in the meta-analysis. The pooled MDs were 39.48 (95%CI: 152.31, 406.47, p < 0.00001), 21.32 (95% CI: –6.04, 48.68, p = 0.13), and 36.46 (95% CI: 21.77, 51.15, p < 0.00001) in the patients with HCC compared to the controls, the patients with LC and those with CH, respectively.

Conclusions
An elevated serum IL-8 level in the HCC patients compared to the three other groups showed an increased risk for this cytokine in HCC patients. Therefore, this interleukin can be used as a new biomarker replacing alpha-fetoprotein (AFP) or as a clinical assay for evaluation of the pathogenesis and probably the progression or development of HCC.

keywords:

hepatocellular carcinoma, chronic hepatitis, liver cirrhosis, cytokine

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