Candidate Genetic Markers of Schizophrenia Based on Exome Sequencing Data and Its Relation to Immunological, Clinical, and Morphometric Changes in the Russian Population.
S M Rastorguev, S V Tsygankova, M A Kaidan, V L Ushakov, I K Malashenkova, S A Krynskiy, D P Ogurtsov, N A Hailov, N V Zakharova, G P Kostyuk
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引用次数: 0
Abstract
The aim of the study was to identify genetic markers of schizophrenia based on exome sequencing data, as well as to specify its potential relation to clinical manifestations of the disease, morphological changes in the brain and immune disorders.
Materials and methods: The analyzed sample consisted of 48 patients (23 men and 25 women; average age - 31.5±7.7 years) having a confirmed diagnosis of paranoid schizophrenia.
Results: 140 genes with differential polymorphisms and enriched categories that may be related to the pathogenesis of schizophrenia were identified. Analysis of genes with differential frequencies of functionally significant common single nucleotide polymorphisms (SNPs) by their major functions showed that the most common were genes involved in regulation of immune system functions and development of the nervous system, as well as genes being structural components of neurons and glia involved in the perception of sensory stimuli. The findings confirm the complexity of the genetic basis of schizophrenia. Analysis of the top 10 genes containing the most differential polymorphisms specifies such genes related to schizophrenia as MUC12 and SH3KBP1. The genes involved in regulation of the immune response include HLA-DQB2 which is one of the most significantly different SNPs between the group of patients and the general population; HLA-DQB2 SNP (rs9276572) in patients is related to the signs of dysfunction of the antiviral component of immune system, structural changes in the brain and cognitive challenges. Although most of the detected genes are unique to the sample studied, additional studies are required to confirm these genes' involvement in the pathogenesis of this disease as well as to identify the mechanisms of the disease onset and development. The rs9276572(C) polymorphism of HLA-DQB2 requires further study as a new potential marker of immunological disorders, morphometric changes in the brain and cognitive impairment in schizophrenia. The data obtained indicate the need for personalized medicine, because the majority of genetic prerequisites are patient-specific and highlight the importance of further research to understand the genetic aspects of schizophrenia and develop innovative approaches to its diagnosis and treatment.
该研究的目的是根据外显子组测序数据确定精神分裂症的遗传标记,并明确其与疾病的临床表现、大脑形态学变化和免疫紊乱的潜在关系。材料与方法:分析48例患者,其中男性23例,女性25例;平均年龄- 31.5±7.7岁)确诊为偏执型精神分裂症。结果:鉴定出140个可能与精神分裂症发病机制相关的差异多态性基因和丰富类别。对功能显著的常见单核苷酸多态性(snp)基因的主要功能差异频率分析表明,最常见的是参与免疫系统功能调节和神经系统发育的基因,以及参与感觉刺激感知的神经元和神经胶质的结构成分基因。这些发现证实了精神分裂症遗传基础的复杂性。对含有最多差异多态性的前10个基因的分析表明,与精神分裂症相关的基因包括MUC12和SH3KBP1。参与调节免疫反应的基因包括HLA-DQB2,这是患者群体与普通人群之间最显着差异的snp之一;患者HLA-DQB2 SNP (rs9276572)与免疫系统抗病毒成分功能障碍、大脑结构变化和认知挑战的迹象有关。虽然大多数检测到的基因是所研究样本所特有的,但需要进一步的研究来证实这些基因参与这种疾病的发病机制,并确定疾病的发生和发展机制。HLA-DQB2 rs9276572(C)多态性作为精神分裂症患者免疫障碍、脑形态改变和认知障碍的潜在新标志物有待进一步研究。获得的数据表明需要个性化医疗,因为大多数遗传先决条件都是针对患者的,并强调了进一步研究以了解精神分裂症的遗传方面并开发其诊断和治疗的创新方法的重要性。