Alcohol Dose Effects on Brain Circuits During Simulated Driving: An fMRI Study

被引:54
作者
Meda, Shashwath A. [1 ]
Calhoun, Vince D. [2 ,3 ,4 ,5 ]
Astur, Robert S. [2 ]
Turner, Beth M.
Ruopp, Kathryn
Pearlson, Godfrey D. [2 ,3 ]
机构
[1] Hartford Hosp, Inst Living, IOL, Olin Neuropsychiat Res Ctr, Hartford, CT 06106 USA
[2] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA
[3] Johns Hopkins Univ, Dept Psychiat, Baltimore, MD USA
[4] Mind Res Network, Albuquerque, NM USA
[5] Univ New Mexico, Dept Elect & Comp Engn, Albuquerque, NM 87131 USA
基金
美国国家卫生研究院;
关键词
ICA; virtual reality; DWI; driving behavior; functional imaging; DEFAULT-MODE; FUNCTIONAL MRI; BASAL GANGLIA; WORKING-MEMORY; ACTIVATION; BEHAVIOR; PERFORMANCE; ATTENTION; TASK; TIME;
D O I
10.1002/hbm.20591
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Driving while intoxicated remains a major public health hazard. Driving is a complex task involving Simultaneous recruitment Of multiple cognitive functions. The investigators studied the neutral substrates of driving and their response to different blood alcohol concentrations (BACs), using functional magnetic resonance imaging (fMRI) and a virtual reality driving simulator. We used independent component analysis (ICA) to isolate spatially independent and temporally correlated driving-related brain circuits in 40 healthy, adult moderate social drinkers. Each subject received three individualized, separate single-blind doses of beverage alcohol to produce BACs of 0.05% (moderate), 0.10%, (high), or 0%, (placebo). 3 T fMRI scanning and continuous behavioral measurement Occurred during simulated driving. Brain function was assessed and compared using both ICA and a conventional general linear model (GLM) analysis. ICA results replicated and significantly extended our previous 1.5T study (Calhoun et al. [2004a]: Neuropsychopharmacology 29:2097-2017). GLM analysis revealed significant dose-related functional differences, complementing ICA data. Driving behaviors including opposite white line crossings and mean speed independently demonstrated significant dose-dependent changes. Behavior-based factors also predicted a frontal-basal-temporal circuit to be functionally impaired with alcohol dosage across baseline scaled, good versus poorly performing drivers. We report neural correlates of driving behavior and found dose-related spatio-temporal disruptions in critical driving-associated regions including the Superior, middle and orbito frontal gyri, anterior cingulate, primary/supplementary motor areas, basal ganglia, and cerebellum. Overall, results Suggest that alcohol (especially at high doses) causes significant impairment of both driving behavior and brain functionality related to motor planning and control, goal directedness, error monitoring, and memory. Hum Brain Mapp 30:1257-1270, 2009. (C) 2008 Wiley-Liss, Inc.
引用
收藏
页码:1257 / 1270
页数:14
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