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      Extrinsic functional connectivity of the default mode network in crack-cocaine users

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          Abstract

          Objective

          This study aimed to explore the functional connectivity of the default mode network (DMN) in crack-cocaine users, in comparison with that observed in age-matched non-drug-using controls.

          Materials and Methods

          Inpatient crack-cocaine users who had been abstinent for at least four weeks and age-matched non-drug-using controls underwent resting state functional magnetic resonance imaging. Images were acquired while the subjects rested with their eyes closed. After data preprocessing, DMNs were defined by spatial independent component analysis and seed-based correlation analysis, by chosen regions of interest centered in the ventral anterior cingulate cortex and in the posterior cingulate cortex.

          Results

          The functional connectivity of the DMN determined by independent component analysis did not differ between the crack-cocaine users and the controls. However, the seed-based correlation analysis seeking a single metric of functional connectivity between specific brain regions showed that the negative connectivity between the ventral anterior cingulate cortex and the left superior parietal lobule was significantly greater in the crack-cocaine users than in the controls.

          Conclusion

          The results suggest that selective extrinsic network connectivity of the DMN related to motor and executive function is impaired during crack-cocaine addiction.

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          Most cited references25

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          Dysfunction of the prefrontal cortex in addiction: neuroimaging findings and clinical implications.

          The loss of control over drug intake that occurs in addiction was initially believed to result from disruption of subcortical reward circuits. However, imaging studies in addictive behaviours have identified a key involvement of the prefrontal cortex (PFC) both through its regulation of limbic reward regions and its involvement in higher-order executive function (for example, self-control, salience attribution and awareness). This Review focuses on functional neuroimaging studies conducted in the past decade that have expanded our understanding of the involvement of the PFC in drug addiction. Disruption of the PFC in addiction underlies not only compulsive drug taking but also accounts for the disadvantageous behaviours that are associated with addiction and the erosion of free will.
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            Advances and Pitfalls in the Analysis and Interpretation of Resting-State FMRI Data

            The last 15 years have witnessed a steady increase in the number of resting-state functional neuroimaging studies. The connectivity patterns of multiple functional, distributed, large-scale networks of brain dynamics have been recognised for their potential as useful tools in the domain of systems and other neurosciences. The application of functional connectivity methods to areas such as cognitive psychology, clinical diagnosis and treatment progression has yielded promising preliminary results, but is yet to be fully realised. This is due, in part, to an array of methodological and interpretative issues that remain to be resolved. We here present a review of the methods most commonly applied in this rapidly advancing field, such as seed-based correlation analysis and independent component analysis, along with examples of their use at the individual subject and group analysis levels and a discussion of practical and theoretical issues arising from this data ‘explosion’. We describe the similarities and differences across these varied statistical approaches to processing resting-state functional magnetic resonance imaging signals, and conclude that further technical optimisation and experimental refinement is required in order to fully delineate and characterise the gross complexity of the human neural functional architecture.
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              Superior parietal cortex is critical for the manipulation of information in working memory.

              In recent years, theoretical perspectives on posterior parietal function have evolved beyond the traditional visuospatial processing models to include more diverse cognitive operations, such as long-term and working memory. However, definitive neuropsychological evidence supporting the superior parietal lobule's purported role in working memory has been lacking. Here, we studied human brain lesion patients to determine whether the superior parietal lobule is indeed necessary for working memory. We assessed a wide range of memory functions in three participant groups: superior parietal lesions (n = 19), lesions not involving superior parietal cortex (n = 146), and no brain lesions (n = 55). Superior parietal damage was reliably associated with deficits on tests involving the manipulation and rearrangement of information in working memory, but not on working memory tests requiring only rehearsal and retrieval processes, nor on tests of long-term memory. These results indicate that superior parietal cortex is critically important for the manipulation of information in working memory.
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                Author and article information

                Journal
                Radiol Bras
                Radiol Bras
                rb
                Radiologia Brasileira
                Colégio Brasileiro de Radiologia e Diagnóstico por Imagem
                0100-3984
                1678-7099
                Jan-Feb 2018
                Jan-Feb 2018
                : 51
                : 1
                : 1-7
                Affiliations
                [1 ]MD, Department of Internal Medicine, Health Sciences Center, Graduate Program in Medicine, Federal University of Espírito Santo (UFES), Vitória, ES, Brazil.
                [2 ]Department of Electric Engineering, Technology Center, Brazilian Research Group on Brain and Cognitive Engineering (BRAEN), Federal University of Espírito Santo (UFES), Vitória, ES, Brazil.
                [3 ]MD, MSc, Laboratory of Cognitive Sciences and Neuropsychopharmacology, Graduate Program in Physiological Sciences, Federal University of Espírito Santo (UFES), Vitória, ES, Brazil.
                [4 ]Laboratory for Medical Research 44 (LIM-44-Laboratório de Investigação Médica 44), Department of Radiology, University of São Paulo (USP), São Paulo, SP, Brazil.
                [5 ]MD, MSc, Department of Internal Medicine, Health Sciences Center, Brazilian Research Group on Brain and Cognitive Engineering (BRAEN), Federal University of Espírito Santo (UFES), Vitória, ES, Brazil.
                [6 ]MD, PhD, Graduate Program in Medicine, Laboratory of Cognitive Sciences and Neuropsychopharmacology, Brazilian Research Group on Brain and Cognitive Engineering (BRAEN), Federal University of Espírito Santo (UFES), Vitória, ES, Brazil.
                Author notes
                Mailing address: Dra. Ester M. Nakamura-Palacios. Programa de Pós-Graduação em Ciências Fisiológicas, Centro de Ciências da Saúde, Universidade Federal do Espírito Santo. Avenida Marechal Campos, 1468, Maruípe. Vitória, ES, Brazil, 29043-900. E-mail: emnpalacios@gmail.com.
                Article
                10.1590/0100-3984.2016.0115
                5846319
                0fa5b11e-9c4e-446b-9898-81dcdd79a5f2

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

                History
                : 05 July 2016
                : 10 January 2017
                Funding
                Funded by: CNPq
                Award ID: 475232/2013-5
                Award ID: 443824/2014-2
                Award ID: 466650/2014-0
                Award ID: 304374/2014-8
                Study conducted under the auspices of the Graduate Program in Physiological Sciences, Federal University of Espírito Santo (UFES), Vitória, ES, Brazil. This work was partially supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-Grant Nos. 475232/2013-5, 443824/2014-2, and 466650/2014-0 to E.M.N-P.). E.M.N-P. is the recipient of a research fellowship grant from CNPq (Grant No. 304374/2014-8).
                Categories
                Original Articles

                substance-related disorders,magnetic resonance imaging/methods,brain/physiopathology,image interpretation, computer-assisted,functional neuroimaging

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