Rangaswamy Madhavi, Porjesz Bernice, Chorlian David B, Wang Kongming, Jones Kevin A, Kuperman Samuel, Rohrbaugh John, O'Connor Sean J, Bauer Lance O, Reich Theodore, Begleiter Henri
Department of Psychiatry, State University of New York, Health Science Center at Brooklyn (SUNY/HSCB), Box 1203, 450 Clarkson Avenue, Brooklyn, NY 11203, USA.
Int J Psychophysiol. 2004 Feb;51(3):239-51. doi: 10.1016/j.ijpsycho.2003.09.003.
This study examines the differences in beta (12-28 Hz) band power in offspring of male alcoholics from densely affected alcoholic families. We have attempted to investigate if the increase in beta power is a 'state' or 'trait' marker for alcoholism. This study also explores the gender differences in the expression of this potential risk marker. Absolute beta power in three bands-beta 1(12-16 Hz), beta 2 (16-20 Hz), and beta 3 (20-28 Hz)-in the eyes closed EEG of 171 high risk (HR) subjects who were offspring of male alcoholics and 204 low risk (LR) subjects with no family history of alcoholism, were compared for each gender separately using a repeated measures analysis of variance design. Alcoholic and non-alcoholic subjects within the high risk group were compared using a repeated measures design as a follow-up analysis. The present study demonstrated increased beta power in the resting EEG of offspring of male alcoholics. Male HR subjects had higher beta 1 (12-16 Hz) power and female HR subjects had increased power in beta 2 (16-20 Hz) and beta 3 (20-28 Hz) as compared with low risk participants. Female HR subjects also showed significantly increased beta 2 and beta 3 power if they had two or more alcoholic first-degree relatives when compared with HR females having only an affected father. Risk characteristics are expressed differentially in males and females and may be an index of differential vulnerability to alcoholism. The results indicate that increased EEG beta power can be considered as a likely marker of risk for developing alcoholism and may be used as a predictive endophenotype.
本研究考察了来自酒精中毒高发家庭的男性酒精中毒者后代在β波(12 - 28赫兹)频段的功率差异。我们试图探究β波功率增加是酒精中毒的“状态”标记还是“特质”标记。本研究还探讨了这种潜在风险标记表达中的性别差异。对171名高风险(HR)受试者(男性酒精中毒者的后代)和204名低风险(LR)受试者(无酒精中毒家族史)闭眼脑电图中三个频段——β1(12 - 16赫兹)、β2(16 - 20赫兹)和β3(20 - 28赫兹)的绝对β波功率,分别按性别使用重复测量方差分析设计进行比较。作为后续分析,对高风险组内的酒精中毒和非酒精中毒受试者使用重复测量设计进行比较。本研究表明,男性酒精中毒者后代静息脑电图中的β波功率增加。与低风险参与者相比,男性HR受试者的β1(12 - 16赫兹)功率更高,女性HR受试者的β2(16 - 20赫兹)和β3(20 - 28赫兹)功率增加。与仅有受影响父亲的HR女性相比,有两个或更多酒精中毒一级亲属的女性HR受试者的β2和β3功率也显著增加。风险特征在男性和女性中的表现不同,可能是对酒精中毒易感性差异的一个指标。结果表明,脑电图β波功率增加可被视为发展为酒精中毒风险的一个可能标记,并可用作预测性内表型。