Serum hepatitis B virus DNA levels differentiating inactive carriers from patients with chronic hepatitis B

被引:18
作者
Seo, Y
Yoon, S
Truong, BX
Kato, H
Hamano, K
Kato, M
Yano, Y
Katayama, M
Ninomiya, T
Hayashi, Y
Kasuga, M
机构
[1] Kobe Univ, Grad Sch Med, Dept Clin Mol Med, Div Diabet Digest & Kidney Dis,Chuo Ku, Kobe, Hyogo 6500017, Japan
[2] Kobe Univ, Grad Sch Med, ICMR, Div Mol Med & Med Genet, Kobe, Hyogo 6500017, Japan
关键词
chronic hepatitis B; HBV-DNA levels; inactive carrier; quantitative polymerase chain reaction assay;
D O I
10.1097/01.meg.0000170926.83850.dd
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective We compared serum hepatitis B virus (HBV)-DNA levels in different states of hepatitis B infection, and investigated whether there is an HBV-DNA value that can be used for differentiating inactive carriers from patients with hepatitis B e antigen (HBeAg)-negative chronic hepatitis. Methods A retrospective study using sera at a followed endpoint from 64 Japanese patients with chronic HBV infection seen in Kobe University Hospital between 1989 and 2002. Sera of patients were assayed using a polymerase chain reaction-based assay. Results Genotype C was dominant (95.4%). Patients with chronic hepatitis with an elevation of the serum alanine aminotransferase (ALT) level had significantly higher HBV-DNA levels than patients with persistently normal ALT. For one time observation at a followed endpoint, the mean HBV-DNA level of HBeAg-negative inactive carriers was significantly lower than that of HBeAg-negative chronic hepatitis patients (3.6 +/- 1.0 versus 4.8 +/- 1.5 log copies/mi, P < 0.005). The use of a cutoff value of 4.5 or 5.0 log copies/ml misclassified 23 and 18% of HBeAg-negative inactive carriers and 50 and 55% of patients with HBeAg-negative chronic hepatitis. If testing were performed on two occasions with approximately a 4-month interval, the cutoff values of 4.5 and 5.0 log copies/ml would misclassify 20 and 10% of HBeAg-negative inactive carriers and 28.6 and 28.6% of patients with HBeAg-negative chronic hepatitis. Conclusions The measurement of serum HBV DNA more than twice is useful for assessing chronic hepatitis B surface antigen carriers and confirms that 105 copies/ml may be an appropriate level of HBV for characterizing the inactive carrier state.
引用
收藏
页码:753 / 757
页数:5
相关论文
共 18 条
[11]   Serum hepatitis B virus DNA levels and liver histology in inactive HBsAg carriers [J].
Martinot-Peignoux, M ;
Boyer, N ;
Colombat, M ;
Akremi, R ;
Pham, BN ;
Ollivier, S ;
Castelnau, C ;
Valla, D ;
Degott, C ;
Marcellin, P .
JOURNAL OF HEPATOLOGY, 2002, 36 (04) :543-546
[12]   Hepatitis B virus genotype assignment using restriction fragment length polymorphism patterns [J].
Mizokami, M ;
Nakano, T ;
Orito, E ;
Tanaka, Y ;
Sakugawa, H ;
Mukaide, M ;
Robertson, BH .
FEBS LETTERS, 1999, 450 (1-2) :66-71
[13]   Long-term follow-up of HBeAg-positive patients treated with interferon alfa for chronic hepatitis B [J].
Niederau, C ;
Heintges, T ;
Lange, S ;
Goldmann, G ;
Niederau, CM ;
Mohr, L ;
Haussinger, D .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (22) :1422-1427
[14]  
Niitsuma H, 1997, AM J GASTROENTEROL, V92, P119
[15]   Automated quantitative analysis of hepatitis B virus DNA by using the cobas Amplicor HBV Monitor test [J].
Noborg, U ;
Gusdal, A ;
Pisa, EK ;
Hedrum, A ;
Lindh, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (09) :2793-2797
[16]   Geographic distribution of hepatitis B virus (HBV) genotype in patients with chronic HBV infection in Japan [J].
Orito, E ;
Ichida, T ;
Sakugawa, H ;
Sata, M ;
Horiike, N ;
Hino, K ;
Okita, K ;
Okanoue, T ;
Iino, S ;
Tanaka, E ;
Suzuki, K ;
Watanabe, H ;
Hige, S ;
Mizokami, M .
HEPATOLOGY, 2001, 34 (03) :590-594
[17]   QUANTIFICATION OF HEPATITIS-B VIRUS-DNA OVER A WIDE-RANGE FROM SERUM FOR STUDYING VIRAL REPLICATIVE ACTIVITY IN RESPONSE TO TREATMENT AND IN RECURRENT INFECTION [J].
RANKI, M ;
SCHATZL, HM ;
ZACHOVAL, R ;
UUSIOUKARI, M ;
LEHTOVAARA, P .
HEPATOLOGY, 1995, 21 (06) :1492-1499
[18]   Hepatitis B virus DNA in anti-HBe-positive asymptomatic carriers [J].
Seo, Y ;
Yoon, S ;
Nakaji, M ;
Yano, Y ;
Nagano, H ;
Ninomiya, T ;
Hayashi, Y ;
Kasuga, M .
INTERVIROLOGY, 2003, 46 (01) :43-49