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      Striatal activity and reduced white matter increase frontal activity in youths with family histories of alcohol and other substance-use disorders performing a go/no-go task

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          Abstract

          Introduction

          Youths with a family history of alcohol and other drug use disorders (FH+) are at greater risk of developing substance-use disorders relative to those with no such family histories (FH−). We previously reported that FH+ youths have elevated activity in the supplementary motor area (SMA) and dorsal striatum while performing go/no-go tasks and have reduced frontal white matter integrity. A better understanding of relationships between these variables would provide insight into how frontostriatal circuitry is altered in FH+ youths, which may be an important contributor to their elevated risk.

          Methods

          In this study, we used structural equation modeling (SEM) to test interactions between activity in the SMA and dorsal striatum in 72 FH+ and 32 FH− youths during go/no-go task performance and to determine whether increased activity in these regions in FH+ youths can be at least partially explained by reduced frontal white matter integrity, as indexed by anterior corona radiata fractional anisotropy and N-acetylaspartate.

          Results

          Increased dorsal striatum activity explained most (∽75%) of the elevated SMA activity in FH+ youths, and the combined contributions of increased dorsal striatal activity, and decreased white matter integrity fully explained the elevated SMA activity.

          Conclusions

          These results suggest the elevated frontal cortical activity in FH+ youths is driven both by their increased striatal activity via downstream projections and reduced white matter integrity in frontal cortical projections, the latter likely increasing frontal cortical activity due to increased energy demands required for action potential propagation. As part of our ongoing longitudinal studies we will examine how these frontostriatal alterations relate to risk for developing substance-use disorders.

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          Most cited references43

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          Factor analysis and AIC

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            Decision-making in the adolescent brain.

            Adolescence is characterized by making risky decisions. Early lesion and neuroimaging studies in adults pointed to the ventromedial prefrontal cortex and related structures as having a key role in decision-making. More recent studies have fractionated decision-making processes into its various components, including the representation of value, response selection (including inter-temporal choice and cognitive control), associative learning, and affective and social aspects. These different aspects of decision-making have been the focus of investigation in recent studies of the adolescent brain. Evidence points to a dissociation between the relatively slow, linear development of impulse control and response inhibition during adolescence versus the nonlinear development of the reward system, which is often hyper-responsive to rewards in adolescence. This suggests that decision-making in adolescence may be particularly modulated by emotion and social factors, for example, when adolescents are with peers or in other affective ('hot') contexts.
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              Frontal-subcortical neuronal circuits and clinical neuropsychiatry: an update.

              Frontal-subcortical circuits form the principal network, which mediate motor activity and behavior in humans. Five parallel frontal-subcortical circuits link the specific areas of the frontal cortex to the striatum, basal ganglia and thalamus. These frontal-subcortical circuits originate from the supplementary motor area, frontal eye field, dorsolateral prefrontal region, lateral orbitofrontal region and anterior cingulate portion of the frontal cortex. The open afferent and efferent connections to the frontal-subcortical circuits mediate coordination between functionally similar areas of the brain. Specific chemoarchitecture and multiple neurotransmitter interactions modulate the functional activity of each circuit. Dorsolateral prefrontal circuit lesions cause executive dysfunction, orbitofrontal circuit lesions lead to personality changes characterized by disinhibition and anterior cingulate circuit lesions present with apathy. The neurobiological correlates of neuropsychiatric disorders including depression, obsessive-compulsive disorder, schizophrenia and substance abuse, imply involvement of frontal-subcortical circuits.
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                Author and article information

                Journal
                Brain Behav
                Brain Behav
                brb3
                Brain and Behavior
                John Wiley & Sons, Ltd (Chichester, UK )
                2162-3279
                2162-3279
                July 2015
                28 May 2015
                : 5
                : 7
                : e00352
                Affiliations
                [1 ]Department of Psychiatry, University of Texas Health Science Center at San Antonio San Antonio, Texas
                [2 ]Research Imaging Institute, University of Texas Health Science Center at San Antonio San Antonio, Texas
                [3 ]Department of Psychiatry, Maryland Psychiatric Research Center, University of Maryland School of Medicine Baltimore, Maryland
                [4 ]Oxford Centre for Functional MRI of the Brain, University of Oxford Oxford, UK
                [5 ]Department of Psychiatry, Yale University School of Medicine New Haven, Connecticut
                [6 ]Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University Baltimore, Maryland
                Author notes
                Correspondence Ashley Acheson, Department of Psychiatry and Research Imaging Institute, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, MC 6240, San Antonio, TX 78229. Tel: (210)567 2741; Fax: (210)567 8152; E-mail: acheson@ 123456uthscsa.edu

                Funding Information Research reported in this publication was supported by NIDA, NIBIB, and NIMH of the National Institutes of Health under award numbers R01-DA026868, R01-DA033997, R01-EB015611, and R01-MH081181. Donald Dougherty is the recipient of the William and Marguerite Wurzbach Distinguished Professorship.

                Article
                10.1002/brb3.352
                4511289
                22200e18-f684-4486-b701-c16d9c6f9634
                © 2015 The Authors. Brain and Behavior published by Wiley Periodicals, Inc.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 19 January 2015
                : 02 March 2015
                : 14 April 2015
                Categories
                Original Research

                Neurosciences
                family history,functional magnetic resonance imaging,go/no-go task,risk,substance use,white matter integrity

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