Show simple item record

Outcome of hepatitis C virus infection in Chinese paid plasma donors: A 12–19‐year cohort study

dc.contributor.authorRao, Hui‐Yingen_US
dc.contributor.authorSun, De‐Guien_US
dc.contributor.authorYang, Rui‐Fengen_US
dc.contributor.authorLiu, Fengen_US
dc.contributor.authorWang, Jianen_US
dc.contributor.authorFeng, Boen_US
dc.contributor.authorWu, Nanen_US
dc.contributor.authorFang, Ji-Lianen_US
dc.contributor.authorSong, Guang‐Junen_US
dc.contributor.authorMa, Huien_US
dc.contributor.authorGuo, Fangen_US
dc.contributor.authorWang, Jiang‐Huaen_US
dc.contributor.authorLi, Xiao‐Boen_US
dc.contributor.authorJin, Qianen_US
dc.contributor.authorQin, Hongen_US
dc.contributor.authorZhuang, Huien_US
dc.contributor.authorWei, Laien_US
dc.date.accessioned2012-03-16T16:02:05Z
dc.date.available2013-05-01T17:24:43Zen_US
dc.date.issued2012-03en_US
dc.identifier.citationRao, Hui‐ying ; Sun, De‐gui ; Yang, Rui‐feng ; Liu, Feng; Wang, Jian; Feng, Bo; Wu, Nan; Fang, Ji‐lian ; Song, Guang‐jun ; Ma, Hui; Guo, Fang; Wang, Jiang‐hua ; Li, Xiao‐bo ; Jin, Qian; Qin, Hong; Zhuang, Hui; Wei, Lai (2012). "Outcome of hepatitis C virus infection in Chinese paid plasma donors: A 12â 19â year cohort study." Journal of Gastroenterology and Hepatology 27(3). <http://hdl.handle.net/2027.42/90418>en_US
dc.identifier.issn0815-9319en_US
dc.identifier.issn1440-1746en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/90418
dc.description.abstractBackground and Aims:  Commercial plasma donation was introduced in China in the 1970s. Cases of non‐A, non‐B hepatitis (hepatitis C) continued to occur, with multiple outbreaks among plasma donors in Guan county, Hebei province between 1972 and 1990. The outcomes of hepatitis C virus (HCV) infection in these paid plasma donors from six villages of Guan county were followed up for 12–19 years. Methods:  A total of 402 plasma donors with HCV infection were enrolled since anti‐HCV‐positive in 1991 or 1998. Follow up was maintained until death or the end of the observation period. No antiviral treatment was applied during the period of infection. Results:  Follow up was lost in 23 cases. After a 12–19‐year follow up, 31 donors died, with the cause of death directly related to liver disease in 15 cases, and an overall mortality of 8.18% (31/379). The incidence of liver cirrhosis was 10.03%, and hepatocellular carcinoma (HCC) was 2.90%. The rate of viral spontaneous clearing was 20.32% (77/379), and 13.69% (23/168) in males and 25.59% (54/211) in females. In May 2010, detections were performed in 348 cases. Abnormality of liver function was related to HCV viremia. Sex and alcohol intake impacted the outcome of HCV infection. There was no correlation between the viral spontaneous clearance with age of infection and genotype. Conclusions:  This area has a high rate of chronicity in HCV infection due to plasma donation. Twenty‐five years after virus infection, liver cirrhosis or HCC developed in one‐tenth of patients, with an overall mortality of 8.18%.en_US
dc.publisherBlackwell Publishing Asiaen_US
dc.publisherWiley Periodicals, Inc.en_US
dc.subject.otherPlasma Donoren_US
dc.subject.otherHepatitis C Virusen_US
dc.subject.otherOutcomeen_US
dc.titleOutcome of hepatitis C virus infection in Chinese paid plasma donors: A 12–19‐year cohort studyen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumPeking University Health Science Center–University of Michigan Health System, Joint Institute for Translational and Clinical Research, Beijing, Chinaen_US
dc.contributor.affiliationotherDepartment of Microbiology, Peking University Health Science Center, Beijing, Chinaen_US
dc.contributor.affiliationotherGuan County Center for Disease Control and Prevention, Hebei Guan, Chinaen_US
dc.contributor.affiliationotherPeking University People's Hospital, Peking University Hepatology Institute, Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Diseases, Beijing, Chinaen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/90418/1/j.1440-1746.2011.06880.x.pdf
dc.identifier.doi10.1111/j.1440-1746.2011.06880.xen_US
dc.identifier.sourceJournal of Gastroenterology and Hepatologyen_US
dc.identifier.citedreferenceMazzeo C, Azzaroli F, Giovanelli S et al. Ten year incidence of HCV infection in northern Italy and frequency of spontaneous viral clearance. Gut 2003; 52: 1030 – 4.en_US
dc.identifier.citedreferenceAscione A, Tartaglione T, Giuseppe Di Costanzo G. Natural history of chronic hepatitis C virus infection. Dig. Liver Dis. 2007; 39 (Suppl. 1 ): S4 – 7.en_US
dc.identifier.citedreferenceSweeting MJ, De Angelis D, Brant LJ, Harris HE, Mann AG, Ramsay ME. The burden of hepatitis C in England. J. Viral Hepat. 2007; 14: 570 – 6.en_US
dc.identifier.citedreferenceGlobal Burden of Hepatitis C Working Group. Global burden of disease for hepatitis C. J. Clin. Pharmacol. 2004; 44: 20 – 9.en_US
dc.identifier.citedreferenceSeeff LB. Natural history of hepatitis C. Am. J. Med. 1999; 107: S10 – 15.en_US
dc.identifier.citedreferenceWiese M, Grungreiff K, Guthoff W, Lafrenz M, Oesen U, Porst H. Outcome in a hepatitis C (genotype 1b) single source outbreak in Germany a 25‐year multicenter study. J. Hepatol. 2005; 43: 590 – 8.en_US
dc.identifier.citedreferenceSeeff LB, Buskell‐Bales Z, Wright EC et al. Long‐term mortality after transfusion‐associated non‐A, non‐B hepatitis. The National Heart, Lung, and Blood Institute Study Group. N. Engl. J. Med. 1992; 327: 1906 – 11.en_US
dc.identifier.citedreferenceKenny‐Walsh E. Clinical outcomes after hepatitis C infection from contaminated anti‐D immune globulin. Irish Hepatology Research Group. N. Engl. J. Med. 1999; 340: 1228 – 33.en_US
dc.identifier.citedreferenceVogt M, Lang T, Frosner G et al. Prevalence and clinical outcome of hepatitis C infection in children who underwent cardiac surgery before the implementation of blood‐donor screening. N. Engl. J. Med. 1999; 341: 866 – 70.en_US
dc.identifier.citedreferenceThomas DL, Astemborski J, Rai RM et al. The natural history of hepatitis C virus infection: host, viral, and environmental factors. JAMA 2000; 284: 450 – 6.en_US
dc.identifier.citedreferenceFerenci P, Ferenci S, Datz C, Rezman I, Oberaigner W, Strauss R. Morbidity and mortality in paid Austrian plasma donors infected with hepatitis C at plasma donation in the 1970s. J. Hepatol. 2007; 47: 31 – 6.en_US
dc.identifier.citedreferenceDu SC, Tao QM, Zhu L. Typing on 5′‐terminal noncoding region of hepatitis C virus genome with restrict endonuclease. Zhonghua Yixue Zazhi 1993; 73: 7 – 9.en_US
dc.identifier.citedreferenceLin DY, Sheen IS, Chiu CT, Lin SM, Kuo YC, Liaw YF. Ultrasonographic changes of early liver cirrhosis in chronic hepatitis B: a longitudinal study. J. Clin. Ultrasound 1993; 21: 303 – 8.en_US
dc.identifier.citedreferenceCastéra L, Vergniol J, Foucher J et al. Prospective comparison of transient elastography, Fibrotest, APRI, and liver biopsy for the assessment of fibrosis in chronic hepatitis C. Gastroenterology 2005; 128: 343 – 50.en_US
dc.identifier.citedreferenceGhany MG, Strader DB, Thomas DL, Seeff LB, American Association for the Study of Liver Diseases. Diagnosis, management, and treatment of hepatitis C: an update. Hepatology 2009; 49: 1335 – 74.en_US
dc.identifier.citedreferenceBruix J, Sherman M, Practice Guidelines Committee, American Association for the Study of Liver Diseases. Management of hepatocellular carcinoma. Hepatology 2005; 42: 1208 – 36.en_US
dc.identifier.citedreferenceChitturi S, Farrell GC, Hashimoto E et al. Non‐alcoholic fatty liver disease in the Asia‐Pacific region: definitions and overview of proposed guidelines. J. Gastroenterol. Hepatol. 2007; 22: 778 – 87.en_US
dc.identifier.citedreferenceDai ZC, Qi GM. The Viral Hepatitis of China: the Epidemiological of Serous. Beijing: Beijing Scientific and Technical Literature Publishers, 1997.en_US
dc.identifier.citedreferenceCenter for Public Health Surveillance and Information Service, Center for Disease Control and Prevention of China. National data of class a, b and c communicable diseases. Disease Surveillance 2000–2010, 2011.en_US
dc.identifier.citedreferenceYokosuka O, Kojima H, Imazeki F et al. Spontaneous negativation of serum hepatitis C virus RNA is a rare event in type C chronic liver diseases: analysis of HCV RNA in 320 patients who were followed for more than 3 years. J. Hepatol. 1999; 31: 394 – 9.en_US
dc.identifier.citedreferenceFreeman AJ, Dore GJ, Low MG et al. Estimating progression to cirrhosis in chronic hepatitis C virus infection. Hepatology 2001; 34: 809 – 16.en_US
dc.identifier.citedreferenceDeuffic‐Burban S, Poynard T, Valleron AJ. Quantification of fibrosis progression in patients with chronic hepatitis C using a Markov model. J. Viral Hepat. 2002; 9: 114 – 22.en_US
dc.identifier.citedreferenceWiley TE, McCarthy M, Breidi L, McCarthy M, Layden TJ. Impact of alcohol on the histological and clinical progression of hepatitis C infection. Hepatology 1998; 28: 80 – 9.en_US
dc.identifier.citedreferencePoynard T, Ratziu V, Charlotte F, Goodman Z, McHutchison J, Albrecht J. Rates and risk factors of liver fibrosis progression in patients with chronic hepatitis C. J. Hepatol. 2001; 34: 730 – 9.en_US
dc.identifier.citedreferenceHarris HE, Ramsay ME, Andrews N, Eldridge KP. Clinical course of hepatitis C virus during the first decade of infection: cohort study. BMJ 2002; 324: 450 – 3.en_US
dc.identifier.citedreferenceSzabo G, Aloman C, Polyak SJ, Weinman SA, Wands J, Zakhari S. Hepatitis C infection and alcohol use: a dangerous mix for the liver and antiviral immunity. Alcohol. Clin. Exp. Res. 2006; 30: 709 – 19.en_US
dc.identifier.citedreferencePeters MG, Terrault NA. Alcohol use and hepatitis C. Hepatology 2002; 36: S220 – 5.en_US
dc.identifier.citedreferenceMinola E, Prati D, Suter F et al. Age at infection affects the longterm outcome of transfusion‐associated chronic hepatitis C. Blood 2002; 99: 4588 – 91.en_US
dc.identifier.citedreferenceBellentani S, Tiribelli C. The spectrum of liver disease in the general population: lesson from the Dionysos study. J. Hepatol. 2001; 35: 531 – 7.en_US
dc.identifier.citedreferenceWei L, Wang QX, Xu XY et al. 12–25‐year follow‐up of hepatitis C virus infection in a rural area of Hebei province, China. Beijing Daxue Xuebao 2002; 34: 574 – 8.en_US
dc.identifier.citedreferenceSeo YS, Um SH, Suh SJ et al. Changes in liver stiffness during the course of acute hepatitis A. Korean J. Hepatol. 2008; 14: 465 – 73.en_US
dc.identifier.citedreferenceTakaki A, Wiese M, Maertens G et al. Cellular immune responses persist and humoral responses decrease two decades after recovery from a single‐source outbreak of hepatitis C. Nat. Med. 2000; 6: 578 – 82.en_US
dc.identifier.citedreferenceSeeff LB, Hollinger FB, Alter HJ et al. Long‐term mortality and morbidity of transfusion‐associated non‐A, non‐B and type C hepatitis: a National Heart, Lung, and Blood Institute collaborative study. Hepatology 2001; 33: 455 – 6.en_US
dc.identifier.citedreferenceAlter HJ. HCV natural history: the retrospective and prospective in perspective. J. Hepatol. 2005; 43: 550 – 2.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.