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HIV-1感染患者免疫和病毒学状态的马尔可夫模型

Markov modelling of immunological and virological states in HIV-1 infected patients.

作者信息

Mathieu E, Loup P, Dellamonica P, Daures J P

机构信息

Clinical Research University Institute, Biostatistics Laboratory, 641 avenue D.G. Giraud, 34093 Montpellier, France.

出版信息

Biom J. 2005 Dec;47(6):834-46. doi: 10.1002/bimj.200410164.

Abstract

The purpose of this study was to evaluate the evolution of HIV infected patients and to bring out some significant factors associated with this pathology. The main criteria revealing the State of illness is viral load measurement (VL). However the CD4 lymphocytes also represent an important marker as these reflect the State of the immune reservoir. Many studies have been carried out in this field and different models have been proposed with a view to a better understanding of this disease. Multi State Markov models defined in terms of CD4 counts, or in terms of viral load, have proved to be very useful tools for modelling HIV disease progression. The model we have developed in this study is based on both the CD4 lymphocytes counts and VL. Markov models are characterized by transition intensities. In this paper we explored several structures in succession. First, we used a homogeneous continuous time Markov process with four states defined by crossed values of CD4 and VL in a given patient at a given time. Then, the effect of certain covariates on the infection process was introduced into the model via the transition intensity functions, as with a Cox regression model. Since the hypothesis of homogeneity may be unrealistic in certain cases, we also considered piecewise homogeneous Markov models. Finally, the effects of covariates and time were combined in a piecewise homogeneous model with a covariate. We applied these methods to data from 1313 HIV-infected patients included in the NADIS cohort.

摘要

本研究的目的是评估艾滋病毒感染患者的病情演变,并找出与这种病症相关的一些重要因素。揭示病情状况的主要标准是病毒载量测量(VL)。然而,CD4淋巴细胞也是一个重要指标,因为它们反映了免疫储备的状况。该领域已经开展了许多研究,并提出了不同的模型,以期更好地理解这种疾病。根据CD4计数或病毒载量定义的多状态马尔可夫模型已被证明是模拟艾滋病毒疾病进展的非常有用的工具。我们在本研究中开发的模型基于CD4淋巴细胞计数和病毒载量。马尔可夫模型的特点是转移强度。在本文中,我们依次探索了几种结构。首先,我们使用了一个齐次连续时间马尔可夫过程,该过程具有四个状态,由给定患者在给定时间的CD4和病毒载量的交叉值定义。然后,如同Cox回归模型一样,通过转移强度函数将某些协变量对感染过程的影响引入模型。由于齐次性假设在某些情况下可能不现实,我们还考虑了分段齐次马尔可夫模型。最后,在一个带有协变量的分段齐次模型中结合了协变量和时间的影响。我们将这些方法应用于纳入NADIS队列的1313名艾滋病毒感染患者的数据。

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