Hepatitis C virus core antigen, an earlier and stronger predictor on sustained virological response in patients with genotype 1 HCV infection

被引:9
作者
Feng, Bo [1 ]
Yang, Rui-Feng [1 ]
Xie, Qing [2 ]
Shang, Jia [3 ]
Kong, Fan-Yun [1 ]
Zhang, Hai-Ying [1 ]
Rao, Hui-Ying [1 ]
Jin, Qian [1 ]
Cong, Xu [1 ]
Liu, Yun-Ye [2 ]
Kang, Yi [3 ]
Wei, Lai [1 ]
机构
[1] Peking Univ, Beijing Key Lab Hepatitis & Immunotherapy Liver D, Peoples Hosp, Inst Hepatol, Beijing 100871, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Infect Dis, Shanghai 200030, Peoples R China
[3] Henan Prov Peoples Hosp, Dept Infect Dis, Zhengzhou, Peoples R China
基金
北京市自然科学基金;
关键词
Hepatitis C; HCV core antigen; Antiviral treatment; Interferon-alpha; PEGINTERFERON ALPHA-2A; DIAGNOSIS; MANAGEMENT; RNA;
D O I
10.1186/1471-230X-14-47
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background: Earlier kinetics of serum HCV core antigen (HCVcAg) and its predictive value on sustained virological response (SVR) were investigated in patients with genotype 1 HCV infection during antiviral treatment. Methods: In a multi-centered, randomized and positive drug-controlled phase IIb clinical trial on type Y peginterferon alpha-2b (NCT01140997), forty-eight CHC patients who participated in pharmacokinetics were randomly divided into 4 cohorts and treated with PegIFN alpha (type Y peginterferon alpha-2b 90 mu g, 135 mu g, 180 mu g and PegIFN alpha-2a 180 mu g, respectively, once a week) and ribavirin (< 75 kg, 1000 mg daily and >= 75 kg, 1200 mg daily) for 48 weeks, and then followed up for 24 weeks. 32 patients infected with genotype 1 HCV and completed the whole process were included in this study. HCV RNAs were detected at baseline, and weeks 4, 12, 24, 48 and 72 using Cobas TaqMan. ARCHITECT HCVcAg was performed at 24, 48, 72, 96, 120 and 144 h in addition to the above time points. The receiver operating curves (ROCs) were performed to study the predictive values of HCVcAg decline on SVR. Results: Following antiviral treatment, serum HCVcAg levels rapidly declined within the first week and correlated well with corresponding HCV RNA at baseline, weeks 4, 12, 24, 48 and 72 (r(s) = 0.969, 0.928, 0.999, 0.983, 0.985 and 0.946, respectively, P < 0.001). All of the areas under the receiver operating curves (AUROCs) were more than 0.80 and showed good predictive power on SVR at 24, 48, 72, 96, 120 and 144 h. The144 h was the best predictive time point of HCVcAg decline on SVR because of its largest AUROC (more than 0.90). Conclusions: Early kinetics of serum HCVcAg predicts SVR very well in genotype 1 CHC patients during antiviral treatment, and its reduction value at 144 h is an earlier and stronger predictor on SVR than rapid virological response and early virological response. (TRN: NCT01140997).
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页数:8
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