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一种功能性神经调节蛋白-1基因变体与应激性生活事件:在一项具有纵向人群代表性的队列研究中对药物使用的影响。

A functional neuregulin-1 gene variant and stressful life events: Effect on drug use in a longitudinal population-representative cohort study.

作者信息

Vaht Mariliis, Laas Kariina, Kiive Evelyn, Parik Jüri, Veidebaum Toomas, Harro Jaanus

机构信息

1 Division of Neuropsychopharmacology, Department of Psychology, Estonian Centre of Behavioural and Health Sciences, University of Tartu, Tartu, Estonia.

2 Division of Special Education, Department of Education, University of Tartu, Tartu, Estonia.

出版信息

J Psychopharmacol. 2017 Jan;31(1):54-61. doi: 10.1177/0269881116655979. Epub 2016 Jul 10.

Abstract

BACKGROUND

The neuregulin 1 gene is a susceptibility gene for substance dependence. A functional polymorphism (SNP8NRG243177/rs6994992; C/T) in the promoter region of the brain-specific type IV neuregulin-1 gene ( NRG1) has been associated with psychiatric disorders (e.g. schizophrenia and bipolar disorder) that often present higher odds of smoking, alcohol and illicit drug use. This study assessed the association of the NRG1 genotype with drug use and possible interaction with stressful life events (SLEs).

METHODS

The database of the Estonian Children Personality Behaviour and Health Study (beginning in 1998) was used. Cohorts of children initially 9 years old ( n=583; followed up at 15 and 18 years) and 15 years old ( n=593; followed up at 18 and 25 years) provided self-reports on alcohol, tobacco and illicit substance use and SLEs. Psychiatric assessment based on DSM-IV was carried out on the older birth cohort at age 25 to assess the lifetime presence of substance use disorders. NRG1 rs6994992 was genotyped in all participants by TaqMan® Pre-Designed SNP Genotyping Assay on the Applied Biosystems ViiA™ 7 Real-Time PCR System. The minor (T) allele frequency was 0.37.

RESULTS

NRG1 rs6994992 C/C homozygotes, especially those who had experienced more SLEs, were more likely to develop alcohol use disorders by young adulthood, were generally more active consumers of tobacco products, and had more likely used illicit drugs. In T allele carriers, SLEs had a negligible effect on substance use.

CONCLUSIONS

In humans, NRG1 genotype is associated with substance use, and this relationship is moderated by adverse life events, with a gain-of-function allele being protective.

摘要

背景

神经调节蛋白1基因是物质依赖的易感基因。脑特异性IV型神经调节蛋白1基因(NRG1)启动子区域的一个功能性多态性(SNP8NRG243177/rs6994992;C/T)与精神疾病(如精神分裂症和双相情感障碍)相关,而这些精神疾病患者通常有更高的吸烟、饮酒和使用非法药物的几率。本研究评估了NRG1基因型与药物使用的关联以及与应激性生活事件(SLEs)的可能相互作用。

方法

使用爱沙尼亚儿童个性行为与健康研究(始于1998年)的数据库。最初9岁的儿童队列(n = 583;在15岁和18岁时进行随访)和15岁的儿童队列(n = 593;在18岁和25岁时进行随访)提供了关于酒精、烟草和非法物质使用以及SLEs的自我报告。对年龄较大的出生队列在25岁时进行基于《精神疾病诊断与统计手册》第四版(DSM-IV)的精神评估,以评估物质使用障碍的终生患病率。通过应用生物系统公司ViiA™ 7实时PCR系统上的TaqMan®预设计SNP基因分型检测对所有参与者进行NRG1 rs6994992基因分型。次要(T)等位基因频率为0.37。

结果

NRG1 rs6994992 C/C纯合子,尤其是那些经历了更多SLEs的人,在成年早期更有可能发展为酒精使用障碍,总体上是烟草产品的更活跃消费者,并且更有可能使用非法药物。在T等位基因携带者中,SLEs对物质使用的影响可忽略不计。

结论

在人类中,NRG1基因型与物质使用相关,并且这种关系受到不良生活事件的调节,功能获得性等位基因具有保护作用。

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