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. 2016:2016:7476231.
doi: 10.1155/2016/7476231. Epub 2016 Aug 30.

Clinical Impact of Viral Load on the Development of Hepatocellular Carcinoma and Liver-Related Mortality in Patients with Hepatitis C Virus Infection

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Clinical Impact of Viral Load on the Development of Hepatocellular Carcinoma and Liver-Related Mortality in Patients with Hepatitis C Virus Infection

Ran Noh et al. Gastroenterol Res Pract. 2016.

Abstract

Aim. This study aimed to assess clinical impact of hepatitis C viral load on the development of hepatocellular carcinoma (HCC) and liver-related mortality in HCV-infected patients. Methods. A total of 111 subjects with chronic HCV infection who were available for serum quantitation of HCV RNA were recruited in this retrospective cohort. Cox-proportional hazards models were used to calculate hazard ratio (HR) of developing HCC and liver-related mortality according to serum HCV RNA titers. Results. HCC was developed in 14 patients during follow-up period. The cumulative risk of HCC development was higher in subjects with high HCV RNA titer (log HCV RNA IU/mL > 6) than subjects with low titer (log HCV RNA IU/mL ≦ 6) (HR = 4.63, P = 0.032), giving an incidence rate of 474.1 and 111.5 per 10,000 person-years, respectively. Old age (HR = 9.71, P = 0.014), accompanying cirrhosis (HR = 19.34, P = 0.004), and low platelet count (HR = 13.97, P = 0.009) were other independent risk factors for the development of HCC. Liver-related death occurred in 7 patients. Accompanying cirrhosis (HR = 6.13, P = 0.012) and low albumin level (HR = 9.17, P = 0.002), but not HCV RNA titer, were significant risk factors related to liver-related mortality. Conclusion. Serum HCV RNA titer may be considered an independent risk factor for the development of HCC but not liver-related mortality.

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Figures

Figure 1
Figure 1
Schematic flow of the recruitment of study participants.
Figure 2
Figure 2
Cumulative incidence of hepatocellular carcinoma according to the viral load of serum HCV RNA. The cumulative incidence rate of HCC in patients with high viral load (log HCV RNA IU/mL > 6) was significantly higher than that in patients with low viral load (log HCV RNA IU/mL ≦ 6) (P = 0.032).
Figure 3
Figure 3
Cumulative liver-related mortality according to the viral load of serum HCV RNA. No significant difference of cumulative liver-related mortality was seen in patients with high or low viral load (P = 0.675).

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References

    1. Poynard T., Bedossa P., Opolon P. Natural history of liver fibrosis progression in patients with chronic hepatitis C. The Lancet. 1997;349(9055):825–832. doi: 10.1016/s0140-6736(96)07642-8. - DOI - PubMed
    1. Perz J. F., Armstrong G. L., Farrington L. A., Hutin Y. J. F., Bell B. P. The contributions of hepatitis B virus and hepatitis C virus infections to cirrhosis and primary liver cancer worldwide. Journal of Hepatology. 2006;45(4):529–538. doi: 10.1016/j.jhep.2006.05.013. - DOI - PubMed
    1. Memon M. I., Memon M. A. Hepatitis C: an epidemiological review. Journal of Viral Hepatitis. 2002;9(2):84–100. doi: 10.1046/j.1365-2893.2002.00329.x. - DOI - PubMed
    1. Lauer G. M., Walker B. D. Hepatitis C virus infection. The New England Journal of Medicine. 2001;345(1):41–52. doi: 10.1056/nejm200107053450107. - DOI - PubMed
    1. Lee M.-S., Kim D.-H., Kim H., et al. Hepatitis B vaccination and reduced risk of primary liver cancer among male adults: a cohort study in Korea. International Journal of Epidemiology. 1998;27(2):316–319. doi: 10.1093/ije/27.2.316. - DOI - PubMed

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