Epworth嗜睡量表(ESS)评分与血清素转运体(5-HTT- LPR、5-HTT- vntr)和昼夜节律(PER3-VNTR)基因的相关性分析

IF 1 Q4 CLINICAL NEUROLOGY Sleep Science Pub Date : 2021-04-15 DOI:10.5935/1984-0063.20220003
F. Ozen, Z. Yeğin, Z. Sağlam, F. Yavlal, H. Koç, Celal Ulaşoğlu
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引用次数: 0

摘要

白天过度嗜睡(EDS)是临床实践中常见的主诉,它会增加机动车事故、工作相关事件和死亡的比例,对个人和社会都有严重的后果。此外,它还表现出不太严重的个人后果。本研究旨在探讨PER3-VNTR、5- httr - lpr和5- httr - vntr在构成EDS责任方面的潜在作用。研究招募了218名参与者(93人抱怨白天困倦,125人没有严重的抱怨)。用Epworth嗜睡量表(ESS)对白天一般嗜睡进行量化。采用标准盐析程序从采集的血液样本中提取DNA并进行基因分型。睡眠障碍组与非睡眠障碍组的ESS评分差异分别为12.75±4.55和6.34±4.26。PER3- VNTR和5-HTT-LPR基因型与ESS平均评分没有相关性。然而,5-HTT-VNTR基因型与ESS平均评分显著相关;具有10/10基因型的个体的ESS得分最高,反映了该基因型是EDS的一个危险因素。我们强烈建议进一步研究不同人群的昼夜/血清素通路基因,以达成共识,并突出睡眠遗传标记基因,这些基因可以成为未来睡眠问题药物治疗研究的目标。
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Association analysis of Epworth Sleepiness Scale (ESS) scores with serotonin transporter (5-HTT- LPR, 5-HTT-VNTR) and circadian (PER3-VNTR) genes
Excessive daytime sleepiness (EDS) is a common complaint encountered in clinical practice with serious consequences both for individual and society since it can increase the ratio of motor vehicle accidents, work- related incidents, and deaths. Moreover, it also manifests less serious individual consequences. This study aimed to investigate the potential role of PER3-VNTR, 5-HTT-LPR, and 5-HTT-VNTR in terms of constituting liability to EDS. Two hundred eighteen participants (93 complaining about daytime sleepiness and 125 individuals with no serious complaint) were recruited in the study. General daytime of sleepiness was quantified with Epworth sleepiness scale (ESS). DNA extractions were performed from collected blood samples with standart salting-out procedure and genotyped. ESS scores displayed difference between individuals suffering from sleep disturbances and other individuals with values of 12.75±4.55 and 6.34±4.26, respectively. PER3- VNTR and 5-HTT-LPR genotypes did not display association with mean ESS scores. However, 5-HTT-VNTR genotypes showed significant association with mean ESS scores; individuals with 10/10 genotypes had the highest ESS score reflecting this genotype as a liability factor for EDS. We strongly recommend further studies based on circadian/serotonin pathway genes in different populations to reach to a consensus and highlight sleep genetic marker genes which then can be the future targets of pharmacological treatment studies for sleep problems.
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来源期刊
Sleep Science
Sleep Science CLINICAL NEUROLOGY-
CiteScore
2.50
自引率
12.50%
发文量
124
审稿时长
10 weeks
期刊最新文献
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