Prefrontal cortex modulation using transcranial DC stimulation reduces alcohol craving: A double-blind, sham-controlled study

被引:266
作者
Boggio, Paulo S. [2 ]
Sultani, Natasha [2 ]
Fecteau, Shirley [1 ]
Merabet, Lotfi [1 ]
Mecca, Tatiana [2 ]
Pascual-Leone, Alvaro [1 ]
Basaglia, Aline [3 ]
Fregni, Felipe [1 ]
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Ctr Noninvas Brain Stimulat, Boston, MA 02215 USA
[2] Univ Prebiteriana Mackenzie, Nucleo Neurociencias, Sao Paulo, Brazil
[3] Univ Sao Paulo, Inst Psychol, Sao Paulo, Brazil
关键词
alcohol craving; brain stimulation; transcranial direct current stimulation; dorsolateral prefrontal cortex;
D O I
10.1016/j.drugalcdep.2007.06.011
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Functional neuroimaging studies have shown that specific brain areas are associated with alcohol craving including the dorsolateral prefrontal cortex (DLPFC). We tested whether modulation of DLPFC using transcranial direct current stimulation (tDCS) could alter alcohol craving in patients with alcohol dependence while being exposed to alcohol cues. Methods: We performed a randomized sham-controlled study in which 13 subjects received sham and active bilateral tDCS delivered to DLPFC (anodal left/cathodal right and anodal right/cathodal left). For sham stimulation, the electrodes were placed at the same positions as in active stimulation; however, the stimulator was turned off after 30 s of stimulation. Subjects were presented videos depicting alcohol consumption to increase alcohol craving. Results: Our results showed that both anodal left/cathodal right and anodal right/cathodal left significantly decreased alcohol craving compared to sham stimulation (p < 0.0001). In addition, we found that following treatment, craving could not be further increased by alcohol cues. Conclusions: Our findings showed that tDCS treatment to DLPFC can reduce alcohol craving. These findings extend the results of previous studies using noninvasive brain stimulation to reduce craving in humans. Given the relatively rapid suppressive effect of tDCS and the highly fluctuating nature of alcohol craving, this technique may prove to be a valuable treatment strategy within the clinical setting. (C) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:55 / 60
页数:6
相关论文
共 37 条
[1]
[Anonymous], 1994, Diagnostic criteria from DSM-IV
[2]
What is the role of dopamine in reward: hedonic impact, reward learning, or incentive salience? [J].
Berridge, KC ;
Robinson, TE .
BRAIN RESEARCH REVIEWS, 1998, 28 (03) :309-369
[3]
Brain metabolic changes during cigarette craving [J].
Brody, AL ;
Mandelkern, MA ;
London, ED ;
Childress, AR ;
Lee, GS ;
Bota, RG ;
Ho, ML ;
Saxena, S ;
Baxter, LR ;
Madsen, D ;
Jarvik, ME .
ARCHIVES OF GENERAL PSYCHIATRY, 2002, 59 (12) :1162-1172
[4]
One session of high frequency repetitive transcranial magnetic stimulation (rTMS) to the right prefrontal cortex transiently reduces cocaine craving [J].
Camprodon, Joan Albert ;
Martinez-Raga, Jose ;
Alonso-Alonso, Miguel ;
Shih, Mei-Chiung ;
Pascual-Leone, Alvaro .
DRUG AND ALCOHOL DEPENDENCE, 2007, 86 (01) :91-94
[5]
DAVIDSON R, 1986, BRIT J ADDICT, V81, P217
[6]
Alcohol urges in alcohol-dependent drinkers: further validation of the Alcohol Urge Questionnaire in an untreated community clinical population [J].
Drummond, DC ;
Phillips, TS .
ADDICTION, 2002, 97 (11) :1465-1472
[7]
Activation in mesolimbic and visuospatial neural circuits elicited by smoking cues: Evidence from functional magnetic resonance imaging [J].
Due, DL ;
Huettel, SA ;
Hall, WG ;
Rubin, DC .
AMERICAN JOURNAL OF PSYCHIATRY, 2002, 159 (06) :954-960
[8]
High-frequency repetitive transcranial magnetic stimulation decreases cigarette smoking [J].
Eichhammer, P ;
Johann, M ;
Kharraz, A ;
Binder, H ;
Pittrow, D ;
Wodarz, N ;
Hajak, G .
JOURNAL OF CLINICAL PSYCHIATRY, 2003, 64 (08) :951-953
[9]
Figlie Neliana Buzi, 2004, Rev. Bras. Psiquiatr., V26, P91, DOI 10.1590/S1516-44462004000200005
[10]
PET imaging studies in drug abuse [J].
Fowler, JS ;
Volkow, ND .
JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY, 1998, 36 (03) :163-174