Biological Determinants of Sleep Disorders

Valery V. Gafarov, Elena A. Gromova, Vladimir N. Maksimov, Igor V. Gagulin, Almira V. Gafarova
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Abstract

The purpose of the study is to research the effect of polymorphism of genes such as CLOCK, ARNTL, PER2, NPAS2, DRD4, DAT, TNF-α, and NPSR1 on sleep disorders in an open population of 25–64-year-old men. We conducted screening studies of representative samples of men aged 25–64 years. The general examination was carried out according to the standard methods included in the WHO MONICA-Psychosocial Program (MOPSY). Carriers of the C/T genotype of the CLOCK gene more often than others reported having “satisfactory” or “poor” sleep. Carriers of the C/T genotype of the ARNTL gene were more likely to experience anxiety dreams, and they woke up exhausted. Carriers of the A/A genotype of the PER2 gene were more likely to wake up two or more times per night, a total of four to seven times per week. In the population, C/T and T/T genotypes of the NPAS2 gene were significantly more common in individuals with 7-hour sleep. Genotype 4/6 of the DRD4 gene and genotype 9/9 of the DAT gene were significantly associated with sleep disturbances. Carriers of the heterozygous A/G genotype of the TNF-α-308 gene, compared with carriers of all other genotypes, more often rated sleep as “satisfactory” (30%) than “good.”
睡眠障碍的生物学决定因素
本研究旨在研究25 - 64岁男性开放人群中CLOCK、ARNTL、PER2、NPAS2、DRD4、DAT、TNF-α、NPSR1等基因多态性对睡眠障碍的影响。我们对25-64岁男性的代表性样本进行了筛选研究。一般检查按照世界卫生组织monica -社会心理规划(MOPSY)的标准方法进行。CLOCK基因的C/T基因型携带者比其他人更常报告睡眠“满意”或“差”。携带ARNTL基因的C/T基因型的人更有可能做焦虑的梦,他们醒来时很疲惫。携带PER2基因A/A基因型的人更有可能每晚醒来两次或两次以上,每周总共醒来四到七次。在人群中,NPAS2基因的C/T和T/T基因型在7小时睡眠的个体中更为常见。DRD4基因4/6型和DAT基因9/9型与睡眠障碍显著相关。TNF-α-308基因杂合A/G基因型的携带者,与所有其他基因型的携带者相比,更多地认为睡眠“满意”(30%)而不是“良好”。
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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