{"title":"分数阶复阶Hopfield神经网络分析HIV感染耐药的影响","authors":"C. Fernández","doi":"10.1109/ICACI49185.2020.9177513","DOIUrl":null,"url":null,"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.","PeriodicalId":346930,"journal":{"name":"International Conference on Advanced Computational Intelligence","volume":"55 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fractional Complex-order Hopfield Neural Networks to Analyze the Effect of Drug-resistance in the HIV Infection\",\"authors\":\"C. Fernández\",\"doi\":\"10.1109/ICACI49185.2020.9177513\",\"DOIUrl\":null,\"url\":null,\"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.\",\"PeriodicalId\":346930,\"journal\":{\"name\":\"International Conference on Advanced Computational Intelligence\",\"volume\":\"55 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Conference on Advanced Computational Intelligence\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/ICACI49185.2020.9177513\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Conference on Advanced Computational Intelligence","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ICACI49185.2020.9177513","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Fractional Complex-order Hopfield Neural Networks to Analyze the Effect of Drug-resistance in the HIV Infection
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.