Genetic Predictors of the Development of Autonomic Dysfunction

K.A. Gazenkampf, E.А. Domoratskaya, D.V. Dmitrenko
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Abstract

Aim: To study the association of the HTR2C gene rs6318, rs6313 of the HTR2A gene, rs4680 of the COMT gene, rs3785143 of the SLC6A2 gene, rs1799913 of the TPH1 gene, rs7997012 of the HTR2A gene with the development of neurotic disorders in young people living in the Krasnoyarsk Territory. Design: A comparative study. Materials and methods. The study included 133 clinically healthy volunteers. The age of the participants ranged from 16 to 24 years. Molecular genetic studies were carried out on the basis of the Laboratory of Medical Genetics of the V.F. Voino-Yasenetsky Moscow State Medical University of the Ministry of Health of Russia. Psychological testing was performed using the questionnaire of depressive symptoms of Beck, the scale of socio-situational anxiety of O. Kondash in the modification of A.M. Parishioner, Hospital scale of anxiety and depression, as well as carrier study of the association of single nucleotide variants (ONV) rs7997012 of the HTR2A gene, rs6318 of the HTR2C gene, rs6313 of the HTR2A gene, rs4680 of the COMT gene, rs3785143 of the SLC6A2 gene, rs1799913 of the TPH1 gene with neurotic disorders (anxiety and subclinical depression). Results. According to multivariate analysis, the association of the COMT G gene allele carrier (odds ratio (OR) = 2.784; 95% confidence interval (CI): 1.291–6.001; χ2 = 6.986; p = 0.009) and the AH genotype (OR = 2,208; 95% CI: 1,032–4,724; χ2 = 16.716; p < 0.001) with subclinical depression according to the total index of the Beck scale. Carrying the SS genotype of the rs1799913 TRN1 gene increases the risk of learning anxiety by 3 times (OR = 3.011; 95% CI: 1.138–7.967; χ2 = 7.622; p = 0.023). Conclusion. The carriage of the G allele and the rs4680 genotype and AG of the COMT gene is associated with subclinical depression, and the carriage of the SS genotype of the rs1799913 TRN1 gene increases the risk of learning anxiety by 3 times. Thus, the ONV of these genes can be considered as predictors of neurotic disorders, significant already at the subclinical level. Keywords: COMT gene, TRN1 gene, anxiety, depression, neurotic disorders.
自主神经功能障碍发展的遗传预测因素
目的:研究克拉斯诺亚尔斯克地区青少年HTR2C基因rs6318、HTR2A基因rs6313、COMT基因rs4680、SLC6A2基因rs3785143、TPH1基因rs1799913、HTR2A基因rs7997012与神经性疾病发生的关系。设计:比较研究。材料和方法。该研究包括133名临床健康志愿者。参与者的年龄从16岁到24岁不等。分子遗传学研究是在俄罗斯卫生部莫斯科国立医科大学V.F. Voino-Yasenetsky医学遗传学实验室的基础上进行的。心理测试采用Beck抑郁症状问卷、O. Kondash社会情境焦虑量表对A.M.进行修改教区居民、医院焦虑和抑郁量表,以及HTR2A基因rs7997012、HTR2C基因rs6318、HTR2A基因rs6313、COMT基因rs4680、SLC6A2基因rs3785143、TPH1基因rs1799913与神经性疾病(焦虑和亚临床抑郁)相关性的载体研究。结果。多因素分析显示,COMT G基因等位基因携带者的相关性(优势比(OR) = 2.784;95%置信区间(CI): 1.291-6.001;χ2 = 6.986;p = 0.009)和AH基因型(OR = 2208;95% ci: 1,032-4,724;χ2 = 16.716;p & lt;0.001),根据贝克量表总指数判定为亚临床抑郁症。携带rs1799913 TRN1基因的SS基因型使学习焦虑的风险增加3倍(OR = 3.011;95% ci: 1.138-7.967;χ2 = 7.622;P = 0.023)。结论。携带G等位基因、COMT基因的rs4680基因型和AG与亚临床抑郁相关,携带rs1799913 TRN1基因的SS基因型使学习焦虑的风险增加3倍。因此,这些基因的ONV可以被认为是神经性疾病的预测因子,在亚临床水平上已经具有重要意义。关键词:COMT基因,TRN1基因,焦虑,抑郁,神经症
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