首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >A model to predict the response to therapy against hepatitis C virus (HCV) including low-density lipoprotein receptor genotype in HIV/HCV-coinfected patients
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A model to predict the response to therapy against hepatitis C virus (HCV) including low-density lipoprotein receptor genotype in HIV/HCV-coinfected patients

机译:预测HIV / HCV合并感染患者对丙型肝炎病毒(HCV)包括低密度脂蛋白受体基因型的治疗反应的模型

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Objectives: Accurate prediction of sustained virological response (SVR) to pegylated interferon-?? (Peg-IFN) plus ribavirin in HIV/hepatitis C virus (HCV)-coinfected patients could improve the management of these patients. We aimed to develop a model to predict SVR to Peg-IFN/ribavirin in HIV/HCV-coinfected individuals combining HCV genotype and baseline HCV RNA load with interleukin 28B and low-density lipoprotein receptor genetic variations. Methods: Three hundred and twelve treatment-naive HIV/HCV-coinfected patients receiving Peg-IFN/ribavirin were analysed in an on-treatment approach. One hundred and eighty-one of them were included in the development group and 131 in the validation population. The predictive model was obtained from a logistic regression equation including the above-mentioned variables. The areas under the receiver operating characteristic (AUROC) curves (95% CI), sensitivity and specificity, as well as negative and positive predictive values, were calculated. Results: SVR was achieved by 88 (48.6%) patients from the development group and 68 (51.9%) individuals from the validation group. The AUROC curve values (95% asymptotic CI) were 0.83 (0.77-0.89) for the development group and 0.84 (0.77-0.91) for the validation group. Using two cut-off values, maximum specificity and sensitivity were 89.7% and 96.6%, respectively, with a negative predictive value for SVR of 88.9% and a positive predictive value of 83.6%. Thirteen (7.2%) individuals were misclassified using these cut-off values. Conclusions: This model represents a reliable and easily applicable tool to individually evaluate the probability of achieving an SVR to Peg-IFN/ribavirin among HIV/HCV-coinfected patients. ? The Author 2012. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved.
机译:目的:准确预测聚乙二醇化干扰素-α的持续病毒学应答(SVR)。 HIV /丙型肝炎病毒(HCV)合并感染的患者中使用(peg-IFN)加利巴韦林可以改善这些患者的治疗。我们旨在建立一个模型,以预测将HIV / HCV合并感染的个体中HCV基因型和基线HCV RNA负荷与白介素28B和低密度脂蛋白受体遗传变异相结合的SVR感染Peg-IFN /利巴韦林的情况。方法:采用治疗方法分析了接受Peg-IFN /利巴韦林治疗的未接受HIV / HCV感染的112例初治患者。其中181个被包括在开发组中,而131个被包括在验证组中。预测模型是从包含上述变量的逻辑回归方程中获得的。计算了接受者工作特征(AUROC)曲线(95%CI),敏感性和特异性以及阴性和阳性预测值下的面积。结果:开发组的88名患者(48.6%)和验证组的68名患者(51.9%)实现了SVR。开发组的AUROC曲线值(95%渐近CI)为0.83(0.77-0.89),验证组的AUROC曲线值为0.84(0.77-0.91)。使用两个临界值,最大特异性和敏感性分别为89.7%和96.6%,SVR的阴性预测值为88.9%,阳性预测值为83.6%。根据这些临界值,有十三(7.2%)个人被错误分类。结论:该模型代表了一种可靠且易于应用的工具,可用于单独评估在HIV / HCV合并感染患者中实现Peg-IFN /利巴韦林SVR的可能性。 ?作者2012。由牛津大学出版社代表英国抗菌化学协会出版。版权所有。

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