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Volume 181, Issue 3, Pages 174-182 (30 March 2010)


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Working memory fMRI activation in cocaine-dependent subjects: Association with treatment response

F. Gerard MoelleraCorresponding Author Informationemail address, Joel L. Steinberga, Joy M. Schmitza, Liangsuo Maa, Shijing Liua, Kimberly L. Kjomea, Nuvan Rathnayakaa, Larry A. Kramerb, Ponnada A. Narayanab

Received 23 June 2009; received in revised form 8 October 2009; accepted 3 November 2009.

Abstract 

Functional magnetic resonance imaging (fMRI) studies of early abstinence cocaine users offer information about the state of the brain when most cocaine users seek treatment. This study examined the relationship between pretreatment brain function and subsequent treatment response in 19 treatment-seeking early abstinence cocaine-dependent (CD) subjects. These subjects and 14 non-drug-using control subjects underwent fMRI while performing a working memory task with three levels of difficulty. CD subjects were then randomized to treatment studies. Results showed CD subjects had significantly lower (random effects, corrected for multiple comparisons) brain activation in caudate, putamen, cingulate gyrus, middle and superior frontal gyri, inferior frontal gyrus pars triangularis and pars opercularis, precentral gyrus, and thalamus compared with non-drug-using controls. Within CD subjects, thalamic activation significantly correlated with treatment response. This study shows CD subjects in early abstinence have alterations of brain function in frontal, striatal, and thalamic brain regions known to be part of a circuit associated with motor control, reward, and cognition. Subjects with pretreatment thalamic deactivation showed the poorest treatment response, possibly related to thalamic involvement in mesocortical and mesolimbic dopamine projections.

a Department of Psychiatry and Behavioral Sciences, University of Texas Health Science Center at Houston, 1300 Moursund, Houston, TX 77030, United States

b Department of Diagnostic and Interventional Imaging, University of Texas Health Science Center at Houston, 6431 Fannin Street, MSB 2.130B, Houston, TX 77030, United States

Corresponding Author InformationCorresponding author. Tel.: +1 713 500 2858; fax: +1 713 500 2618.

PII: S0925-4927(09)00269-8

doi:10.1016/j.pscychresns.2009.11.003


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