首页> 外文期刊>Computational statistics & data analysis >Long-term HIV dynamic models incorporating drug adherence and resistance to treatment for prediction of virological responses
【24h】

Long-term HIV dynamic models incorporating drug adherence and resistance to treatment for prediction of virological responses

机译:结合药物依从性和治疗抗性的长期HIV动态模型,用于预测病毒学应答

获取原文
获取原文并翻译 | 示例
           

摘要

Long-term therapy with antiretroviral (ARV) agents in HIV-infected patients often results in failure to suppress the viral load. Imperfect adherence and drug susceptibility to prescribed antiviral drugs are important factors explaining the resurgence of virus. A better understanding of the factors responsible for the virological failure is critical for the development of new treatment strategies. In this paper, we develop a mechanism-based reparameterized differential equation model for characterizing long-term viral dynamics with ARV therapy. In this model we directly incorporate drug susceptibility and drug adherence (measured by medication event monitoring system (MEMS) and questionnaires) into a function of treatment efficacy. A Bayesian nonlinear mixed-effects modeling approach is investigated for estimating dynamic parameters by fitting the model to viral load data from an AIDS clinical trial. The effects of drug adherence interaction with drug resistance-based models are compared using (i) the sum of the squared residual (SSR) from individual subjects and (ii) the deviance information criterion (DIC), a Bayesian version of the classical deviance for model assessment, designed from complex hierarchical model settings. The results indicate that the drug adherence combined with confounding factor, drug resistance in viral dynamic modeling significantly predict virologic responses. Our study suggests that long-term reparameterized dynamic models are powerful and effective in establishing a relationship of antiviral responses with drug adherence and susceptibility.
机译:在感染HIV的患者中使用抗逆转录病毒(ARV)药物进行长期治疗通常会导致无法抑制病毒载量。对处方抗病毒药物的不完全依从性和药物敏感性是解释病毒复发的重要因素。更好地了解导致病毒学衰竭的因素对于开发新的治疗策略至关重要。在本文中,我们开发了一种基于机制的重新参数化微分方程模型,用于表征ARV治疗的长期病毒动力学。在该模型中,我们将药物敏感性和药物依从性(通过药物事件监测系统(MEMS)和调查表进行测量)直接纳入治疗功效的函数中。通过将模型拟合到来自AIDS临床试验的病毒载量数据,研究了贝叶斯非线性混合效应建模方法来估计动态参数。使用以下方法比较药物依从性与基于耐药性模型的相互作用的影响:(i)来自个体受试者的残差平方和(SSR)和(ii)偏差信息标准(DIC),即经典偏差的贝叶斯版本。模型评估,是根据复杂的分层模型设置设计的。结果表明,病毒动力学模型中的药物依从性与混杂因素,耐药性相结合可显着预测病毒学应答。我们的研究表明,长期重新参数化的动态模型在建立抗病毒反应与药物依从性和易感性之间的关系方面功能强大且有效。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号