TY - JOUR
T1 - Clinical and virological course of chronic hepatitis B virus infection with hepatitis C and D virus markers
AU - Liaw, Yun Fan
AU - Tsai, Sun Lung
AU - Sheen, I. Shyan
AU - Chao, Mei
AU - Yeh, Chau Ting
AU - Hsieh, Sen Yung
AU - Chu, Chia Ming
PY - 1998/3
Y1 - 1998/3
N2 - Objective: Hepatitis B, C, and delta virus (HBV, HCV, HDV) share similar transmission routes; thus, dual or triple infections may occur and even persist in the same patient. However, little is known about the presentations and course of chronic HBV infection with HCV and HDV markers, which this study examined. Methods: Antibodies against HCV (anti-HCV) and HDV (anti- HDV) were assayed as appropriate in patients with HBV infection. The clinical, pathological, and virological presentations as well as the course of the disease in patients with HBV/HDV/HCV triple infection markers were then reviewed. Results: A total of 60 patients, 51 men and nine women, age 19-67 yr (mean 45.9 ± 1.6 yr) were identified. Of these 60 patients, five (8.3%) were HBeAg positive and 10 (16.7%) cirrhotic at entry, 30 (50%) presented with acute superinfection (HCV or HDV, or both) and the remaining 30 presented with chronic liver disease. On presentation, 16 (53.3%) of the 30 patients with acute superinfection showed hepatic decompensation and eight (26.7%) died. In contrast, only one of the patients with 'chronic liver disease' presented with hepatic decompensation. Of the 42 patients followed up for 1-15 (mean, 4.7 ± 0.6) yr, 45.2% showed remission and 19% showed HBeAg seroclearance, whereas 12.5% of the 32 noncirrhotics developed cirrhosis and three of the nine cirrhotics became decompensated. At the end of follow-up, 29 patients (69.9%) were still seropositive for HCV-RNA but only nine (22.5%) were seropositive for HDV-RNA and five (12.5%) were seropositive for HBV-DNA. Conclusions: These results suggest that infection with HBV, HCV, and HDV triple markers is a severe disease in acute superinfection stage but that the course is relatively benign, slowly progressive, and usually dominated by HCV.
AB - Objective: Hepatitis B, C, and delta virus (HBV, HCV, HDV) share similar transmission routes; thus, dual or triple infections may occur and even persist in the same patient. However, little is known about the presentations and course of chronic HBV infection with HCV and HDV markers, which this study examined. Methods: Antibodies against HCV (anti-HCV) and HDV (anti- HDV) were assayed as appropriate in patients with HBV infection. The clinical, pathological, and virological presentations as well as the course of the disease in patients with HBV/HDV/HCV triple infection markers were then reviewed. Results: A total of 60 patients, 51 men and nine women, age 19-67 yr (mean 45.9 ± 1.6 yr) were identified. Of these 60 patients, five (8.3%) were HBeAg positive and 10 (16.7%) cirrhotic at entry, 30 (50%) presented with acute superinfection (HCV or HDV, or both) and the remaining 30 presented with chronic liver disease. On presentation, 16 (53.3%) of the 30 patients with acute superinfection showed hepatic decompensation and eight (26.7%) died. In contrast, only one of the patients with 'chronic liver disease' presented with hepatic decompensation. Of the 42 patients followed up for 1-15 (mean, 4.7 ± 0.6) yr, 45.2% showed remission and 19% showed HBeAg seroclearance, whereas 12.5% of the 32 noncirrhotics developed cirrhosis and three of the nine cirrhotics became decompensated. At the end of follow-up, 29 patients (69.9%) were still seropositive for HCV-RNA but only nine (22.5%) were seropositive for HDV-RNA and five (12.5%) were seropositive for HBV-DNA. Conclusions: These results suggest that infection with HBV, HCV, and HDV triple markers is a severe disease in acute superinfection stage but that the course is relatively benign, slowly progressive, and usually dominated by HCV.
UR - https://www.scopus.com/pages/publications/0032034043
U2 - 10.1016/s0002-9270(97)00104-4
DO - 10.1016/s0002-9270(97)00104-4
M3 - 文章
C2 - 9517639
AN - SCOPUS:0032034043
SN - 0002-9270
VL - 93
SP - 354
EP - 359
JO - American Journal of Gastroenterology
JF - American Journal of Gastroenterology
IS - 3
ER -