Evaluation of quantitative measurements of hepatitis C virus RNA to predict sustained response to interferon by genotype

被引:12
作者
Chayama, K
Suzuki, F
Tsubota, A
Akuta, N
Someya, T
Kobayashi, M
Arase, Y
Saitoh, S
Suzuki, Y
Ikeda, K
Kumada, H
机构
[1] Hiroshima Univ, Fac Med, Dept Internal Med 1, Minnami Ku, Hiroshima 7348551, Japan
[2] Toranomon Gen Hosp, Mem Inst Med Res, Dept Gastroenterol, Minato Ku, Tokyo 105, Japan
关键词
interferon; genotype; viral load; ROC;
D O I
10.1016/S0166-0934(01)00290-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Hepatitis C virus (HCV) virus load is one of the most important predictive factors for the outcome of interferon (IFN) therapy. Recent technological advances have allowed a more precise measurement of HCV load. However, the exact cutoff values that could be used to predict the outcome of IFN have not been established for each assay. Five recent quantitative assays were evaluated for the measurement of HCV (Amplicor monitor ver 1.0. Amplicor monitor ver 2.0 (GT), Amplicor monitor ver 2.0 (Cobas), Quantiplex branched DNA amplification (bDNA) ver 2.0 and HCV core protein level by enzyme immunosorbent assay) in 209 consecutive patients with chronic hepatitis C, who received IFN therapy. The results of the two second generation Amplicor monitor tests (GT and Cobas) showed the best correlation (r = 0.930), but the other tests also showed relatively good correlations (r = 0.646-0.925). Each method predicted the effect of IFN with comparable predictive efficacy, ranging from 77.0 to 80.8%. Receiver operating characteristic (ROC) curve analysis showed that Amplicor monitor ver 2.0 and bDNA ver 2.0 are superior in predicting the response in genotype 2a. The best cutoff value for predicting the response to IFN was different by genotype, which should be considered in selecting candidates for IFN treatment. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:33 / 45
页数:13
相关论文
共 46 条
[1]   Performance of an automated system for quantification of hepatitis C virus RNA [J].
Afonso, AMR ;
Didier, J ;
Plouvier, E ;
Falissard, B ;
Ferey, MP ;
Bogard, M ;
Dussaix, E .
JOURNAL OF VIROLOGICAL METHODS, 2000, 86 (01) :55-60
[2]   Multicenter evaluation of the COBAS AMPLICOR HCV assay, an integrated PCR system for rapid detection of hepatitis C virus RNA in the diagnostic laboratory [J].
Albadalejo, J ;
Alonso, R ;
Antinozzi, R ;
Bogard, M ;
Bourgault, AM ;
Colucci, G ;
Fenner, T ;
Petersen, H ;
Sala, E ;
Vincelette, J ;
Young, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (04) :862-865
[3]   CHRONIC HEPATITIS-C VIRUS-INFECTIONS - PREDICTIVE VALUE OF GENOTYPE AND LEVEL OF VIREMIA ON DISEASE PROGRESSION AND RESPONSE TO INTERFERON-ALPHA [J].
BOOTH, JCL ;
FOSTER, GR ;
KUMAR, U ;
GALASSINI, R ;
GOLDIN, RD ;
BROWN, JL ;
THOMAS, HC .
GUT, 1995, 36 (03) :427-432
[4]   QUANTITATIVE BRANCHED DNA ASSAY AND GENOTYPING FOR HEPATITIS-C VIRUS-RNA IN CHINESE PATIENTS WITH ACUTE AND CHRONIC HEPATITIS-C [J].
CHAN, CY ;
LEE, SD ;
HWANG, SJ ;
LU, RH ;
LU, CL ;
LO, KJ .
JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (02) :443-446
[5]  
CHAYAMA K, 1991, HEPATOLOGY, V13, P1040
[6]   GENOTYPIC SUBTYPING OF HEPATITIS-C VIRUS [J].
CHAYAMA, K ;
TSUBOTA, A ;
ARASE, Y ;
SAITOH, S ;
KOIDA, I ;
IKEDA, K ;
MATSUMOTO, T ;
KOBAYASHI, M ;
IWASAKI, S ;
KOYAMA, S ;
MORINAGA, T ;
KUMADA, H .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1993, 8 (02) :150-156
[7]   Pretreatment virus load and multiple amino acid substitutions in the interferon sensitivity-determining region predict the outcome of interferon treatment in patients with chronic genotype 1b hepatitis C virus infection [J].
Chayama, K ;
Tsubota, A ;
Kobayashi, M ;
Okamoto, K ;
Hashimoto, M ;
Miyano, Y ;
Koike, H ;
Kobayashi, M ;
Koida, I ;
Arase, Y ;
Saitoh, S ;
Suzuki, Y ;
Murashima, N ;
Ikeda, K ;
Kumada, H .
HEPATOLOGY, 1997, 25 (03) :745-749
[8]   PREDICTION OF RESPONSE TO INTERFERON TREATMENT OF CHRONIC HEPATITIS-C [J].
DAVIS, GL .
JOURNAL OF HEPATOLOGY, 1994, 21 (01) :1-3
[9]   TREATMENT OF CHRONIC HEPATITIS-C WITH RECOMBINANT INTERFERON-ALFA - A MULTICENTER RANDOMIZED, CONTROLLED TRIAL [J].
DAVIS, GL ;
BALART, LA ;
SCHIFF, ER ;
LINDSAY, K ;
BODENHEIMER, HC ;
PERRILLO, RP ;
CAREY, W ;
JACOBSON, IM ;
PAYNE, J ;
DIENSTAG, JL ;
VANTHIEL, DH ;
TAMBURRO, C ;
LEFKOWITCH, J ;
ALBRECHT, J ;
MESCHIEVITZ, C ;
ORTEGO, TJ ;
GIBAS, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (22) :1501-1506
[10]   Accurate quantification of hepatitis C virus (HCV) RNA from all HCV genotypes by using branched-DNA technology [J].
Detmer, J ;
Lagier, R ;
Flynn, J ;
Zayati, C ;
Kolberg, J ;
Collins, M ;
Urdea, M ;
SanchezPescador, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (04) :901-907