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Decline in genetic influence on the co-occurrence of alcohol, marijuana, and nicotine dependence symptoms from age 14 to 29.14 岁至 29 岁期间遗传对酒精、大麻和尼古丁依赖症状同时出现的影响下降。
Am J Psychiatry. 2012 Oct;169(10):1073-81. doi: 10.1176/appi.ajp.2012.11081268.
2
The interplay of genes and adolescent development in substance use disorders: leveraging findings from GWAS meta-analyses to test developmental hypotheses about nicotine consumption.基因与青少年发展在物质使用障碍中的相互作用:利用 GWAS 荟萃分析的结果来检验关于尼古丁消费的发展假设。
Hum Genet. 2012 Jun;131(6):791-801. doi: 10.1007/s00439-012-1167-1. Epub 2012 Apr 11.
3
Developmental Endophenotypes: Indexing Genetic Risk for Substance Abuse with the P300 Brain Event-Related Potential.发育性内表型:利用P300脑事件相关电位评估物质滥用的遗传风险
Child Dev Perspect. 2011 Dec 1;5(4):239-247. doi: 10.1111/j.1750-8606.2011.00205.x.
4
The P300 event-related brain potential as a neurobiological endophenotype for substance use disorders: a meta-analytic investigation.P300 事件相关脑电位作为物质使用障碍的神经生物学内表型:一项荟萃分析研究。
Neurosci Biobehav Rev. 2012 Jan;36(1):572-603. doi: 10.1016/j.neubiorev.2011.09.002. Epub 2011 Sep 21.
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The effects of latent variables in the development of comorbidity among common mental disorders.常见精神障碍共病中潜在变量的作用。
Depress Anxiety. 2011 Jan;28(1):29-39. doi: 10.1002/da.20760.
6
Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence.全基因组关联研究theta 波段事件相关振荡发现血清素受体基因 HTR7 影响酒精依赖的风险。
Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):44-58. doi: 10.1002/ajmg.b.31136. Epub 2010 Nov 2.
7
Operationalizing proneness to externalizing psychopathology as a multivariate psychophysiological phenotype.将易患外化性精神病理学表现为多变量心理生理学表型。
Psychophysiology. 2011 Jan;48(1):64-72. doi: 10.1111/j.1469-8986.2010.01047.x.
8
The anatomical and functional relationship between the P3 and autonomic components of the orienting response.定向反应中P3与自主神经成分之间的解剖学和功能关系。
Psychophysiology. 2011 Feb;48(2):162-75. doi: 10.1111/j.1469-8986.2010.01057.x.
9
Relationship between the P3 event-related potential, its associated time-frequency components, and externalizing psychopathology.P3 事件相关电位及其相关时频成分与外化性精神病理学的关系。
Psychophysiology. 2010 Jan 1;47(1):123-32. doi: 10.1111/j.1469-8986.2009.00876.x. Epub 2009 Aug 7.
10
Childhood risk factors for young adult substance dependence outcome in offspring from multiplex alcohol dependence families: a prospective study.多聚酒精依赖家族中青年成物质依赖结局的儿童期风险因素:一项前瞻性研究。
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在一项对14岁青少年进行前瞻性研究的队列中,P300波幅降低与早发性和迟发性病理性物质使用有关。

P300 amplitude reduction is associated with early-onset and late-onset pathological substance use in a prospectively studied cohort of 14-year-old adolescents.

作者信息

Perlman Greg, Markin Abraham, Iacono William G

机构信息

Department of Psychology, University of Minnesota, Minneapolis, Minnesota, USA.

Medical School, University of Minnesota, Minneapolis, Minnesota, USA.

出版信息

Psychophysiology. 2013 Oct;50(10):974-82. doi: 10.1111/psyp.12081. Epub 2013 Aug 2.

DOI:10.1111/psyp.12081
PMID:23905780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3872222/
Abstract

P3 amplitude reduction (P3AR) is associated with risk for adolescent-onset pathological substance use (PSU). In this longitudinal study, data from over 1,100 adolescent twins were used to examine P3AR in relation to early adolescent onset PSU (i.e., by age 14), late adolescent onset PSU (i.e., ages 14-18), misuse of different classes of substances (PSU-nicotine, PSU-alcohol, PSU-illicit), degree of PSU comorbidity, and gender differences. P3 amplitude was recorded at age 14 from two midline electrodes during a visual oddball paradigm. PSU was defined as meeting criteria for any symptom of a substance use disorder assessed using semistructured clinical interviews. P3AR was associated with degree of drug class comorbidity, early adolescent onset PSU for all three substance classes, and late adolescent onset PSU for alcohol and illicit PSU. Gender differences in P3AR were not statistically significant. These findings provide further evidence that P3AR indexes a nonspecific diathesis for adolescent-onset PSU.

摘要

P3波幅降低(P3AR)与青少年期病理性物质使用(PSU)风险相关。在这项纵向研究中,来自1100多名青少年双胞胎的数据被用于检验P3AR与青少年早期开始的PSU(即14岁之前)、青少年晚期开始的PSU(即14 - 18岁)、不同类别物质的滥用(PSU - 尼古丁、PSU - 酒精、PSU - 非法药物)、PSU共病程度以及性别差异之间的关系。在视觉Oddball范式中,于14岁时从两个中线电极记录P3波幅。PSU被定义为符合使用半结构化临床访谈评估的物质使用障碍的任何症状标准。P3AR与药物类别共病程度、所有三类物质的青少年早期开始的PSU以及酒精和非法药物PSU的青少年晚期开始的PSU相关。P3AR的性别差异无统计学意义。这些发现提供了进一步的证据,表明P3AR是青少年期PSU的一种非特异性素质指标。