Lipsitch M, Levin B R
Department of Biology, Emory University, Atlanta, Georgia, USA.
Int J Tuberc Lung Dis. 1998 Mar;2(3):187-99.
Patient non-compliance and/or spatial heterogeneity in drug concentration or effectiveness may contribute to the emergence of drug resistance during multiple-drug chemotherapy of tuberculosis.
Using mathematical models of mycobacterial population dynamics under antimicrobial treatment, to assess the effects of non-compliance, heterogeneity and other factors on the success of treatment.
A mathematical model is used to generate predictions about the ascent of drug resistance in treated hosts with non-compliance and/or a 'protected compartment' of bacteria where only one drug is active; simulations of a more realistic version of this model take into account random mutation, and different assumptions about the size of, and growth rate of bacteria in, the protected compartment.
The existence of a protected compartment can increase the likelihood of resistance to the single drug active in that compartment, but only if bacteria resistant to that drug can grow in the protected compartment or if the host is non-adherent to the treatment regimen. However, the protected compartment may also slow the ascent of bacteria resistant to drugs not active in it (e.g. isoniazid) by providing a reservoir of non-selected mycobacteria. The model predicts that relative rates of killing are more important than mutation rates in determining the order in which resistant mutants ascend. Model predictions, in combination with data about drug resistance patterns, suggest that non-compliance, but not heterogeneity, is an important cause of treatment failure.
Patterns of acquired drug resistance may be used to infer processes of selection during treatment; mathematical models can aid in generating predictions about the relative impacts of treatment parameters in the evolution of resistance, and eventually in suggesting improved treatment protocols.
患者不依从治疗和/或药物浓度或疗效的空间异质性可能导致结核病多药化疗期间耐药性的出现。
利用抗菌治疗下分枝杆菌种群动态的数学模型,评估不依从、异质性和其他因素对治疗成功的影响。
使用数学模型对存在不依从治疗和/或存在一个“受保护区室”(其中只有一种药物有活性)的治疗宿主中耐药性的上升进行预测;对该模型更现实版本的模拟考虑了随机突变以及关于受保护区室中细菌大小和生长速率的不同假设。
受保护区室的存在会增加对该区域中单一活性药物产生耐药性的可能性,但前提是对该药物耐药的细菌能够在受保护区室中生长,或者宿主不遵守治疗方案。然而,受保护区室也可能通过提供未被选择的分枝杆菌库来减缓对其中无活性的药物(如异烟肼)产生耐药性的细菌的上升。该模型预测,在确定耐药突变体出现的顺序时,相对杀灭率比突变率更重要。模型预测与耐药模式数据相结合表明,不依从而非异质性是治疗失败的重要原因。
获得性耐药模式可用于推断治疗期间的选择过程;数学模型有助于对治疗参数在耐药性演变中的相对影响进行预测,并最终有助于提出改进的治疗方案。