2009
DOI: 10.1016/j.trsl.2008.11.008
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Interleukin-18 promoter polymorphisms and the disease progression of Hepatitis B virus-related liver disease

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Cited by 28 publications
(29 citation statements)
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“…A further two studies3839 were excluded because they included either patients with only liver cirrhosis or an aggregated patient population with HCC or liver cirrhosis. In the end, 8 studies1213141516171819 were included in the final meta-analysis based on our search strategy and inclusion criteria (Table 1). Of these 8 studies, all1213141516171819 evaluated the association between the -137 polymorphism and HCC risk (1,318 cases, 2,254 controls), while 7 studies12141516171819 evaluated the association between the -607 polymorphism and HCC risk (1,262 cases, 1,696 controls).…”
Section: Resultsmentioning
confidence: 99%
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“…A further two studies3839 were excluded because they included either patients with only liver cirrhosis or an aggregated patient population with HCC or liver cirrhosis. In the end, 8 studies1213141516171819 were included in the final meta-analysis based on our search strategy and inclusion criteria (Table 1). Of these 8 studies, all1213141516171819 evaluated the association between the -137 polymorphism and HCC risk (1,318 cases, 2,254 controls), while 7 studies12141516171819 evaluated the association between the -607 polymorphism and HCC risk (1,262 cases, 1,696 controls).…”
Section: Resultsmentioning
confidence: 99%
“…Meta-analysis of 7 studies12131416171819 involving 1,206 Asian cases and 2,052 Asian controls showed no evidence of a significant association between the -137 polymorphism and HCC risk for any of the five genetic models (Table 3): allelic, OR 1.01, 95% CI 0.71–1.43, P  = 0.97; recessive model, OR 1.08, 95% CI 0.68–1.70, P  = 0.75; dominant, OR 0.99, 95% CI 0.62–1.57, P  = 0.96; homozygous, OR 1.09, 95% CI 0.69–1.72, P  = 0.73; heterozygous, OR 0.98, 95% CI 0.61–1.56, P  = 0.92. Similarly, no evidence of an association was identified in meta-analysis of 4 studies14171819 involving 832 Chinese cases and 1,151 Chinese controls (Table 3): allelic, OR 0.87, 95% CI 0.54–1.39, P  = 0.56; recessive, OR 0.89, 95% CI 0.49–1.65, P  = 0.72; dominant, OR 0.86, 95% CI 0.45–1.66, P  = 0.66; homozygous, OR 0.80, 95% CI 0.43–1.48, P  = 0.48; heterozygous, OR 0.85, 95% CI 0.44–1.66, P  = 0.64.…”
Section: Resultsmentioning
confidence: 99%
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“…Moreover, the IL-18-607 SNP with AA genotype was accompanied by inhibition of HBV DNA replication [20]. In addition, Migita et al [22] in a study comprised of 204 chronically HBV-infected patients; suggested that IL-18 -607 and -137 had differential outcomes on HBV infection, where they found that these SNPs are significantly higher in inactive HBV carriers compared to those with chronic progressive liver disease. Moreover, Hirankarn et al [23] found that A/A genotype of IL-18-607 SNP (rs1946518) can be used as a new genetic marker in Thai population for prediction of chronic hepatitis B development.…”
Section: Discussionmentioning
confidence: 99%