Fractional Complex-order Hopfield Neural Networks to Analyze the Effect of Drug-resistance in the HIV Infection

C. Fernández
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Abstract

The present paper uses a complex and fractional-order model for Hopfield neural networks to set a nonlinear model that represents the quantity of infected/uninfected CD4+T cells into the HIV dynamic when an antiviral therapy based on protease inhibitors is applied. By using a mathematical model of the environment associated with CD4+T cells that are progressively infected, it is proposed a closed-loop scheme associated with the HIV dynamic and its antiviral therapy, both acting in the same environment. To this end, the work reported here will use Caputo-type derivatives in order to represent such closed-loop dynamic by assuming that there is a nonlinear model based on Hopfield neural networks (HNN). In this way, the mutual interference between the additive activation dynamics of HNN and the complex-valued fractional-order analysis will be used to study the local and global asymptotic stability of HIV. The effect of drug-resistance will be the main starting point to understand how the resistant CD4+T cells can be reduced. The equilibrium point of HNN model will be studied by using quadratic-type Lyapunov functions and compared with a model based on Grunwald-Letnikov formulation in order to validate the approach proposed. The results show that HNN-based model converges toward a small neighborhood of the origin with better performance than Grunwald-Letnikov model.
分数阶复阶Hopfield神经网络分析HIV感染耐药的影响
本文采用复杂分数阶Hopfield神经网络模型,建立了基于蛋白酶抑制剂抗病毒治疗时感染/未感染CD4+T细胞进入HIV动态数量的非线性模型。通过使用与逐渐感染的CD4+T细胞相关的环境的数学模型,提出了一个与HIV动态及其抗病毒治疗相关的闭环方案,两者在相同的环境中起作用。为此,本文将使用caputo型导数来表示这种闭环动态,并假设存在基于Hopfield神经网络(HNN)的非线性模型。这样,将利用HNN的加性激活动力学与复值分数阶分析之间的相互干扰来研究HIV的局部和全局渐近稳定性。耐药性的影响将是了解如何减少耐药CD4+T细胞的主要出发点。利用二次型Lyapunov函数研究HNN模型的平衡点,并与基于Grunwald-Letnikov公式的模型进行比较,以验证所提出的方法。结果表明,基于hnn的模型收敛于原点的小邻域,性能优于Grunwald-Letnikov模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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