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      Interactions between decision-making and emotion in behavioral-variant frontotemporal dementia and Alzheimer’s disease

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          Abstract

          Negative and positive emotions are known to shape decision-making toward more or less impulsive responses, respectively. Decision-making and emotion processing are underpinned by shared brain regions including the ventromedial prefrontal cortex (vmPFC) and the amygdala. How these processes interact at the behavioral and brain levels is still unclear. We used a lesion model to address this question. Study participants included individuals diagnosed with behavioral-variant frontotemporal dementia (bvFTD, n = 18), who typically present deficits in decision-making/emotion processing and atrophy of the vmPFC, individuals with Alzheimer’s disease (AD, n = 12) who present with atrophy in limbic structures and age-matched healthy controls (CTRL, n = 15). Prior to each choice on the delay discounting task participants were cued with a positive, negative or neutral picture and asked to vividly imagine witnessing the event. As hypothesized, our findings showed that bvFTD patients were more impulsive than AD patients and CTRL and did not show any emotion-related modulation of delay discounting rate. In contrast, AD patients showed increased impulsivity when primed by negative emotion. This increased impulsivity was associated with reduced integrity of bilateral amygdala in AD but not in bvFTD. Altogether, our results indicate that decision-making and emotion interact at the level of the amygdala supporting findings from animal studies.

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          Separate neural systems value immediate and delayed monetary rewards.

          When humans are offered the choice between rewards available at different points in time, the relative values of the options are discounted according to their expected delays until delivery. Using functional magnetic resonance imaging, we examined the neural correlates of time discounting while subjects made a series of choices between monetary reward options that varied by delay to delivery. We demonstrate that two separate systems are involved in such decisions. Parts of the limbic system associated with the midbrain dopamine system, including paralimbic cortex, are preferentially activated by decisions involving immediately available rewards. In contrast, regions of the lateral prefrontal cortex and posterior parietal cortex are engaged uniformly by intertemporal choices irrespective of delay. Furthermore, the relative engagement of the two systems is directly associated with subjects' choices, with greater relative fronto-parietal activity when subjects choose longer term options.
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            The brain basis of emotion: a meta-analytic review.

            Researchers have wondered how the brain creates emotions since the early days of psychological science. With a surge of studies in affective neuroscience in recent decades, scientists are poised to answer this question. In this target article, we present a meta-analytic summary of the neuroimaging literature on human emotion. We compare the locationist approach (i.e., the hypothesis that discrete emotion categories consistently and specifically correspond to distinct brain regions) with the psychological constructionist approach (i.e., the hypothesis that discrete emotion categories are constructed of more general brain networks not specific to those categories) to better understand the brain basis of emotion. We review both locationist and psychological constructionist hypotheses of brain-emotion correspondence and report meta-analytic findings bearing on these hypotheses. Overall, we found little evidence that discrete emotion categories can be consistently and specifically localized to distinct brain regions. Instead, we found evidence that is consistent with a psychological constructionist approach to the mind: A set of interacting brain regions commonly involved in basic psychological operations of both an emotional and non-emotional nature are active during emotion experience and perception across a range of discrete emotion categories.
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              Emotion, decision making and the orbitofrontal cortex.

              The somatic marker hypothesis provides a systems-level neuroanatomical and cognitive framework for decision making and the influence on it by emotion. The key idea of this hypothesis is that decision making is a process that is influenced by marker signals that arise in bioregulatory processes, including those that express themselves in emotions and feelings. This influence can occur at multiple levels of operation, some of which occur consciously and some of which occur non-consciously. Here we review studies that confirm various predictions from the hypothesis. The orbitofrontal cortex represents one critical structure in a neural system subserving decision making. Decision making is not mediated by the orbitofrontal cortex alone, but arises from large-scale systems that include other cortical and subcortical components. Such structures include the amygdala, the somatosensory/insular cortices and the peripheral nervous system. Here we focus only on the role of the orbitofrontal cortex in decision making and emotional processing, and the relationship between emotion, decision making and other cognitive functions of the frontal lobe, namely working memory.
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                Author and article information

                Journal
                Soc Cogn Affect Neurosci
                Soc Cogn Affect Neurosci
                scan
                Social Cognitive and Affective Neuroscience
                Oxford University Press
                1749-5016
                1749-5024
                June 2020
                01 July 2020
                01 July 2020
                : 15
                : 6
                : 681-694
                Affiliations
                [1 ] School of Psychology , The University of Sydney , Sydney, Australia
                [2 ] Brain & Mind Centre , The University of Sydney , Sydney, Australia
                [3 ] ARC Centre of Excellence in Cognition & its Disorders , Sydney, Australia
                [4 ] Laboratory for Research in Neuroimaging LREN , Department of Clinical Neurosciences, Lausanne University Hospital and University of Lausanne , Lausanne, Switzerland
                [5 ] Clinical Medical School , The University of Sydney , Sydney, Australia
                Author notes
                Correspondence should be addressed to Aurélie L. Manuel Stocker, Centre Hospitalier Universitaire Vaudois (CHUV), Département des Neurosciences Cliniques, Platerforme Neuroscape@Neurotech, Pavillon 4, Av. de Beaumont, CH-1011 Lausanne. E-mail: Aurelie.Manuel-Stocker@ 123456chuv.ch
                Author information
                http://orcid.org/0000-0002-8301-033X
                Article
                nsaa085
                10.1093/scan/nsaa085
                7393308
                32613246
                55c3815e-9365-4293-9d4d-838dc138886b
                © The Author(s) 2020. Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 13 January 2020
                : 16 May 2020
                : 15 June 2020
                Page count
                Pages: 14
                Funding
                Funded by: National Health and Medical Research Council, DOI 10.13039/501100000925;
                Award ID: APP1037746
                Funded by: Australian Research Council, DOI 10.13039/501100000923;
                Funded by: Disorders Memory Program;
                Award ID: CE11000102
                Award ID: CE110001021
                Funded by: Swiss National Science Foundation, DOI 10.13039/501100001711;
                Award ID: P300P1_171478
                Award ID: P4P4PS_183817
                Funded by: NHMRC Senior Research;
                Award ID: GNT1103258
                Funded by: NHMRC-ARC Dementia Research Development Fellowship;
                Award ID: GNT1097026
                Categories
                AcademicSubjects/SCI01880
                Original Manuscript

                Neurosciences
                delay discounting,emotion,ventromedial prefrontal cortex,amygdala,voxel-based morphometry

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