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首页> 外文期刊>BMC Infectious Diseases >HCV core antigen and HCV-RNA in HIV/HCV co-infected patients with different HCV genotypes
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HCV core antigen and HCV-RNA in HIV/HCV co-infected patients with different HCV genotypes

机译:HIV / HCV共感染不同HCV基因型患者的HCV核心抗原和HCV-RNA

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Background A good correlation between HCV core antigen (HCVAg) and different HCV-RNA assays has been described, but little data are available in HCV/HIV co-infection. We aimed to evaluate HCVAg in comparison with HCV-RNA and to determine their kinetics during antiviral treatment in selected HCV/HIV co-infected patients. Methods 355 samples from 286 HCV/HIV co-infected subjects for whom HCV-RNA (Abbott RealTime) was requested were analysed also for HCVAg (Abbott ARCHITECT) in order to evaluate the correlation between the two parameters both in patients treated or untreated for chronic hepatitis C and according to different HCV genotypes. The differences between percentages were evaluated by chi square or Fisher’s exact test, while mean and median values were compared by Student’s t test or the Mann–Whitney test, respectively. All differences were considered significant for a p value Results HCVAg was detectable on 288/315 sera (91.4%) positive for HCV-RNA and in 5 out of40 (12.5%) sera with undetectable HCV-RNA for a total concordance of 90.1%. The correlation was fair both in untreated (r?=?0.742) and in treated (r?=?0.881) patients and stronger for genotypes 1 and 4 than for genotype 3. Both HCV-RNA and HCVAg levels were significantly higher (p?=?0.028 and p?=?0.0098, respectively) in patients infected by genotype 1 than by genotype 3. The mean ratio of Log values between HCV-RNA (IU/mL) and HCVAg (fmol/liter) was 2.27?±?1.09 in untreated and 2.20?±?0.82 in treated patients (p?=?n.s.),consistent with a sensitivity of HCVAg corresponding to about 1,000?IU/mL of HCV-RNA, and ranged from 2.21 to 2.32 among HCV genotypes with no significant differences; five samples (1.4%; 2 genotype 1a or 1c, 3 genotype 3a) showed highly divergent values. The analysis of 18 monitoring profiles from patients treated with PEG-IFN and Ribavirin showed similar trends, except in one case in which relapse could be predicted by HCVAg and not by HCV-RNA. Conclusion These results suggest that HCVAg represents an adequate tool for determining an ongoing HCV infection also in HIV co-infected patients, with lower costs and faster turnaround time than HCV-RNA.
机译:背景技术已经描述了HCV核心抗原(HCVAg)与不同的HCV-RNA检测方法之间的良好相关性,但是在HCV / HIV合并感染中几乎没有可用的数据。我们旨在评估HCVAg与HCV-RNA的比较,并确定在选定的HCV / HIV合并感染患者中抗病毒治疗期间的动力学。方法对来自286名HCV / HIV合并感染受试者的355份需要HCV-RNA(Abbott RealTime)的样本进行了分析,以评估HCVAg(Abbott ARCHITECT),以评估接受治疗或未经接受治疗的慢性病患者这两个参数之间的相关性丙型肝炎并根据不同的HCV基因型。百分比之间的差异通过卡方检验或Fisher精确检验进行了评估,而均值和中位数分别通过Student t检验或Mann-Whitney检验进行了比较。所有差异均视为p值均显着。结果HCVAg在HCV-RNA阳性的288/315血清中检出(91.4%),在40份血清(12.5%)的血清中有5个检出HCV-RNA,总一致性为90.1%。在未经治疗的患者(r = 0.742)和在治疗的患者(r = 0.881)之间的相关性都是公平的,基因型1和4的相关性强于基因型3。HCV-RNA和HCVAg水平均显着更高(p?基因型1感染的患者比基因型3感染的患者分别分别为= 0.028和p?=?0.0098)。HCV-RNA(IU / mL)和HCVAg(fmol /升)的Log值平均比为2.27?±?。未经治疗的患者为1.09,经治疗的患者为2.20±±0.82(p?=?ns),与HCVAg的敏感性相对应,对应于约1,000?IU / mL HCV-RNA,在无HCV基因型的基因型中介于2.21至2.32之间重大差异; 5个样本(1.4%; 2个基因型1a或1c,3个基因型3a)显示出高度差异的值。对来自接受PEG-IFN和利巴韦林治疗的患者的18个监测图谱的分析显示了相似的趋势,除了在一种情况下可以通过HCVAg而非HCV-RNA预测复发。结论这些结果表明,HCVAg可以作为确定HIV合并感染患者中正在进行的HCV感染的合适工具,与HCV-RNA相比,其成本更低,周转时间更快。

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