精神兴奋剂成瘾患者的个性化康复,考虑到控制血清素系统和神经可塑性脑过程的基因多态性

K. N. Poplevchenkov, T. Agibalova, M. Zastrozhin, O. Buzik
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引用次数: 0

摘要

这项研究的相关性是由于精神兴奋剂成瘾患者每年都在增加,并且缺乏在个性化方法框架内的基于证据的康复方法,该方法考虑了疾病的病理生物标志物状态。该研究的目的是开发一种个性化的方法来治疗精神兴奋剂成瘾患者,同时考虑到控制血清素系统和大脑神经可塑性过程工作的基因多态性。通过对325例精神兴奋剂成瘾患者的研究,发现了控制血清素系统(SLC6A4, HTR2A, HTR2C)和神经可塑性脑过程(BDNF)工作的基因多态性变异,影响依赖性的形成和治疗效果。已经确定,这些基因的多态性与精神兴奋剂成瘾患者康复计划的动机工作的有效性和缓解的持续时间有关。基于所获得的结果,考虑到某些临床和遗传生物标志物以及患者对旨在康复和形成长期缓解的动机性心理治疗的反应特征,确定了精神兴奋剂成瘾患者的个性化概况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Personalized rehabilitation of patients with psychostimulant addiction, taking into account the polymorphism of genes controlling the serotonin system and neuroplastic brain processes
The relevance of this study is due to the annual increase in patients with psychostimulant addiction and the lack of evidence-based methods of their rehabilitation within the framework of a personalized approach that takes into account the state of pathogenetic biomarkers of the disease. The aim of the study is to develop a personalized approach to the rehabilitation of patients with psychostimulant addiction, taking into account the polymorphism of genes controlling the work of the serotonin system and neuroplastic processes of the brain. As a result of the study of 325 patients with psychostimulant addiction, polymorphic variants of genes controlling the work of the serotonin system (SLC6A4, HTR2A, HTR2C) and neuroplastic brain processes (BDNF), affecting the formation of dependence and the effectiveness of therapy, were identified. It has been established that polymorphisms in these genes are associated with the effectiveness of motivational work for the rehabilitation program of patients with psychostimulant addiction and the duration of remissions. Based on the results obtained, personalized profiles of patients with psychostimulant addiction, taking into account certain clinical and genetic biomarkers and features of the response of patients to motivational psychotherapy aimed at rehabilitation and the formation of long-term remission, were identified.
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