齐次半马尔可夫模型在评估纳米比亚抗逆转录病毒治疗患者艾滋病进展中的应用

Simon Pombili Kashihalwa, Josua Mwanyekange, Lilian Pazvakawambwa
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引用次数: 0

摘要

背景:从HIV感染到艾滋病再到死亡的进展可以被认为是一个随机过程。基于CD4计数,疾病进展可以被分解为有限数量的中间状态。HIV/AIDS进展马尔可夫过程的五种状态通常定义为:S1: CD4计数>500个细胞/微升;S2: 350 <CD4计数≤500个细胞/微升;S3: 200 <CD4计数≤350个/微升;S4: CD4计数≤200个细胞/微升;and D: Death. 目的:本研究的目的是利用从卫生和社会服务部获得的数据,利用同质半马尔可夫过程,对纳米比亚接受抗逆转录病毒治疗随访的患者的艾滋病毒/艾滋病疾病进展进行建模。方法:采用回顾性研究设计,收集2422例患者资料,共观察11028次。采用半马尔可夫模型估计过渡概率和过渡强度率。拟合时间齐次半马尔可夫模型,通过比较正向转换和反向转换来评估ART的有效性。 结果:正如预期的那样,从良好状态过渡到较差状态的概率随着时间的推移而增加(6个月后从状态1过渡到状态3和状态4的概率分别为0.023和0.004,12个月后分别为0.059和0.010)。随着时间的增加,处于同一状态的概率逐渐减小(6个月、12个月和18个月后处于状态1的概率分别为0.804、0.698和0.633)。正如预期的那样,强度表明从良好状态向最差状态过渡的速率正在降低(从状态1到状态3和状态4的过渡强度为p<0.001)。TDF/3TC/EFV是状态1向状态2过渡的最强预测因子,其风险比为1.338 (p值为0.002)。服用TDF/3TC/EFV的患者从状态1过渡到状态2的可能性是未服用TDF/3TC/EFV的患者的1.338倍。预测变量女性的风险比为0.678,表明女性比男性更不可能从状态2过渡到状态3。女性从不良状态到较好状态的风险比大于1,这表明与男性相比,女性对治疗的反应较小。 结论:如果不采取干预措施,HIV可迅速发展为艾滋病。早期开始抗逆转录病毒治疗对于减少从良好状态过渡到较差状态的可能性至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Application of Homogenous Semi-Markov Model for Assessing HIV/AIDS Progression to ART Patients in Namibia
Background: The progression of HIV infection to AIDS and then to death can be considered a stochastic process. Disease progression can be broken down into a finite number of intermediate states, based on CD4 counts. The five states of the Markov process of HIV/AIDS progression are commonly defined as: S1: CD4 count > 500 cells/microliter; S2: 350 < CD4 count ≤ 500 cells/microliter; S3: 200 < CD4 count ≤ 350 cells/microliter; S4: CD4 count ≤ 200 cells/microliter; and D: Death. Objectives: The objective of this study was to model the progression of HIV/AIDS disease of patients under ART follow-up in Namibia using homogenous semi-Markov processes, using the data obtained from Ministry of Health and Social Services. Methods: A retrospective study design was used to obtain data on 2422 patients who were observed 11028 times. The semi-Markov model was employed to estimate the transition probabilities and transition intensity rate. Time Homogeneous Semi-Markov model was fitted to assess effectiveness of ART by comparing the forward transition and reverse transitions. Results: As expected the probabilities of transiting from good states to worse states increased with time (from state 1 to state 3 and 4 after 6 months is 0.023 and 0.004, after 12 months is 0.059 and 0.010 respectively). As time increase the probabilities of remaining in the same state is decreasing (probabilities of remaining in state 1 after 6, 12 and 18 months is 0.804, 0.698 and 0.633). As expected the intensity indicates that the rate of transiting from good states to worst states is decreasing (the intensity of transiting from state 1 to 3 and 4 is p<0.001). The strongest predictor of transition from state 1 to 2 is TDF/3TC/EFV, which has a hazard ratio of 1.338 (with p value of 0.002). Patients who were prescribed TDF/3TC/EFV, are over 1.338 times more likely to transit from state 1 to state 2 than patients who did not receive TDF/3TC/EFV. A hazard ratio of 0.678 for the predictor variable female shows that female were less likely to transit from state 2 to 3 than their male counterparts. The hazard ratios of females from a bad state to a better state are more than 1, which is an indication that females are less likely to respond to treatment compared to males. Conclusions: HIV can progress to AIDS without delay if there is no intervention. Early ART initiation is crucial to reduce the probabilities of transiting from good states to worse states.
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