Liu Chun-Jen, Chen Pei-Jer, Shau Wen-Yi, Kao Jia-Horng, Lai Ming-Yang, Chen Ding-Shinn
Department of Internal Medicine, National Taiwan University College of Medicine, National Taiwan University Hospital, 1 Chang-Te Street, Taipei 100, Taiwan.
Liver Int. 2003 Jun;23(3):148-55. doi: 10.1034/j.1600-0676.2003.00820.x.
BACKGROUND/AIM: The natural history of hepatitis-C virus (HCV) infection has been explored in volunteer blood donors, but not yet in hepatitis-B endemic areas. Whether previous or concurrent hepatitis-B virus (HBV) infection influences the natural history of HCV infection remains unknown. Thus, we followed the anti-HCV-positive blood donors who had past or concurrent HBV infection in Taiwan.
From 1992 to 1993, 1588 anti-HCV reactive volunteer blood donors were referred to us from the Taipei Blood Center and 879 (55%) repeatedly reactive for anti-HCV were enrolled. Two hundred and forty-three donors (HCV RNA seropositive rate 49% by polymerase chain reaction (PCR)) received regular follow-ups (mean period: 4.9 years) with their liver disease status determined mainly by clinical and biochemical parameters, serum alpha-fetoprotein level and imaging studies. Hepatitis-C virus genotype and occult HBV infection were determined by PCR-based assays.
Of the initial 879 subjects, 250 (28%) had chronic hepatitis, nine (1%) had liver cirrhosis (LC) and two (0.2%) had hepatocellular carcinoma (HCC) already. In the 243 regularly followed donors, 30% had repeatedly normal serum alanine aminotransferase (ALT) and 70% had more than once elevated ALT. Cirrhosis developed in four (1.6%; follow-up period range: 2-6 years) and HCC in two (0.8%; follow-up period: 3 and 4 years, respectively). Distribution of HCV genotype and hepatitis-B surface antigen (HBsAg) did not differ between those with and those without elevation of ALT. Of the 15 donors with LC and/or HCC, only 1(7%) was positive for both HBsAg and HBV DNA and the other 14 were negative for both HBsAg and serum HBV DNA.
Incidentally detected hepatitis-C was progressive in a small proportion of anti-HCV-positive volunteer blood donors in Taiwan. Occult HBV infection played a minimal role in the development of LC in this donor population.
背景/目的:丙型肝炎病毒(HCV)感染的自然史已在志愿献血者中进行了探索,但尚未在乙型肝炎流行地区进行。既往或同时感染乙型肝炎病毒(HBV)是否会影响HCV感染的自然史仍不清楚。因此,我们对台湾既往或同时感染HBV的抗HCV阳性献血者进行了随访。
1992年至1993年,台北血液中心将1588名抗HCV反应性志愿献血者转介给我们,其中879名(55%)抗HCV反复反应阳性者被纳入研究。243名献血者(聚合酶链反应(PCR)检测HCV RNA血清阳性率为49%)接受了定期随访(平均随访期:4.9年),其肝病状况主要通过临床和生化参数、血清甲胎蛋白水平及影像学检查来确定。通过基于PCR的检测方法确定HCV基因型和隐匿性HBV感染情况。
在最初的879名受试者中,250名(28%)患有慢性肝炎,9名(1%)患有肝硬化(LC),2名(0.2%)已患有肝细胞癌(HCC)。在243名接受定期随访的献血者中,30%的人血清丙氨酸氨基转移酶(ALT)反复正常,70%的人ALT不止一次升高。4人(1.6%;随访期范围:2至6年)发展为肝硬化,2人(0.8%;随访期分别为3年和4年)发展为HCC。ALT升高者与未升高者之间HCV基因型和乙型肝炎表面抗原(HBsAg)的分布无差异。在15名患有LC和/或HCC的献血者中,只有1名(7%)HBsAg和HBV DNA均为阳性,其他14名HBsAg和血清HBV DNA均为阴性。
在台湾,偶然检测到的丙型肝炎在一小部分抗HCV阳性志愿献血者中呈进展性。隐匿性HBV感染在该献血者群体的LC发生中作用极小。