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      The Cerebellar Cognitive Affective/Schmahmann Syndrome: a Task Force Paper

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          Abstract

          Sporadically advocated over the last two centuries, a cerebellar role in cognition and affect has been rigorously established in the past few decades. In the clinical domain, such progress is epitomized by the “cerebellar cognitive affective syndrome” (“CCAS”) or “Schmahmann syndrome.” Introduced in the late 1990s, CCAS reflects a constellation of cerebellar-induced sequelae, comprising deficits in executive function, visuospatial cognition, emotion–affect, and language, over and above speech. The CCAS thus offers excellent grounds to investigate the functional topography of the cerebellum, and, ultimately, illustrate the precise mechanisms by which the cerebellum modulates cognition and affect. The primary objective of this task force paper is thus to stimulate further research in this area. After providing an up-to-date overview of the fundamental findings on cerebellar neurocognition, the paper substantiates the concept of CCAS with recent evidence from different scientific angles, promotes awareness of the CCAS as a clinical entity, and examines our current insight into the therapeutic options available. The paper finally identifies topics of divergence and outstanding questions for further research.

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          Evidence for topographic organization in the cerebellum of motor control versus cognitive and affective processing.

          Patients with cerebellar damage often present with the cerebellar motor syndrome of dysmetria, dysarthria and ataxia, yet cerebellar lesions can also result in the cerebellar cognitive affective syndrome (CCAS), including executive, visual spatial, and linguistic impairments, and affective dysregulation. We have hypothesized that there is topographic organization in the human cerebellum such that the anterior lobe and lobule VIII contain the representation of the sensorimotor cerebellum; lobules VI and VII of the posterior lobe comprise the cognitive cerebellum; and the posterior vermis is the anatomical substrate of the limbic cerebellum. Here we analyze anatomical, functional neuroimaging, and clinical data to test this hypothesis. We find converging lines of evidence supporting regional organization of motor, cognitive, and limbic behaviors in the cerebellum. The cerebellar motor syndrome results when lesions involve the anterior lobe and parts of lobule VI, interrupting cerebellar communication with cerebral and spinal motor systems. Cognitive impairments occur when posterior lobe lesions affect lobules VI and VII (including Crus I, Crus II, and lobule VIIB), disrupting cerebellar modulation of cognitive loops with cerebral association cortices. Neuropsychiatric disorders manifest when vermis lesions deprive cerebro-cerebellar-limbic loops of cerebellar input. We consider this functional topography to be a consequence of the differential arrangement of connections of the cerebellum with the spinal cord, brainstem, and cerebral hemispheres, reflecting cerebellar incorporation into the distributed neural circuits subserving movement, cognition, and emotion. These observations provide testable hypotheses for future investigations. Copyright (c) 2009 Elsevier Srl. All rights reserved.
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            Control of mental activities by internal models in the cerebellum.

            Masao ITO (2008)
            The intricate neuronal circuitry of the cerebellum is thought to encode internal models that reproduce the dynamic properties of body parts. These models are essential for controlling the movement of these body parts: they allow the brain to precisely control the movement without the need for sensory feedback. It is thought that the cerebellum might also encode internal models that reproduce the essential properties of mental representations in the cerebral cortex. This hypothesis suggests a possible mechanism by which intuition and implicit thought might function and explains some of the symptoms that are exhibited by psychiatric patients. This article examines the conceptual bases and experimental evidence for this hypothesis.
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              Functional atlas of emotional faces processing: a voxel-based meta-analysis of 105 functional magnetic resonance imaging studies.

              Most of our social interactions involve perception of emotional information from the faces of other people. Furthermore, such emotional processes are thought to be aberrant in a range of clinical disorders, including psychosis and depression. However, the exact neurofunctional maps underlying emotional facial processing are not well defined. Two independent researchers conducted separate comprehensive PubMed (1990 to May 2008) searches to find all functional magnetic resonance imaging (fMRI) studies using a variant of the emotional faces paradigm in healthy participants. The search terms were: "fMRI AND happy faces," "fMRI AND sad faces," "fMRI AND fearful faces," "fMRI AND angry faces," "fMRI AND disgusted faces" and "fMRI AND neutral faces." We extracted spatial coordinates and inserted them in an electronic database. We performed activation likelihood estimation analysis for voxel-based meta-analyses. Of the originally identified studies, 105 met our inclusion criteria. The overall database consisted of 1785 brain coordinates that yielded an overall sample of 1600 healthy participants. Quantitative voxel-based meta-analysis of brain activation provided neurofunctional maps for 1) main effect of human faces; 2) main effect of emotional valence; and 3) modulatory effect of age, sex, explicit versus implicit processing and magnetic field strength. Processing of emotional faces was associated with increased activation in a number of visual, limbic, temporoparietal and prefrontal areas; the putamen; and the cerebellum. Happy, fearful and sad faces specifically activated the amygdala, whereas angry or disgusted faces had no effect on this brain region. Furthermore, amygdala sensitivity was greater for fearful than for happy or sad faces. Insular activation was selectively reported during processing of disgusted and angry faces. However, insular sensitivity was greater for disgusted than for angry faces. Conversely, neural response in the visual cortex and cerebellum was observable across all emotional conditions. Although the activation likelihood estimation approach is currently one of the most powerful and reliable meta-analytical methods in neuroimaging research, it is insensitive to effect sizes. Our study has detailed neurofunctional maps to use as normative references in future fMRI studies of emotional facial processing in psychiatric populations. We found selective differences between neural networks underlying the basic emotions in limbic and insular brain regions.
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                Author and article information

                Contributors
                georgios.argyropoulos@ndcn.ox.ac.uk
                kimvandun@gmail.com
                michael.adamaszek@klinik-bavaria.de
                maria.leggio@uniroma1.it
                mmanto@ulb.ac.be
                m.masciullo@hsantalucia.it
                m.molinari@hsantalucia.it
                stoodley@american.edu
                Frank.VanOverwalle@vub.ac.be
                ivry@berkeley.edu
                jschmahmann@mgh.harvard.edu
                Journal
                Cerebellum
                Cerebellum
                Cerebellum (London, England)
                Springer US (New York )
                1473-4222
                1473-4230
                14 September 2019
                14 September 2019
                2020
                : 19
                : 1
                : 102-125
                Affiliations
                [1 ]GRID grid.4991.5, ISNI 0000 0004 1936 8948, Nuffield Department of Clinical Neurosciences, , University of Oxford, ; Oxford, UK
                [2 ]GRID grid.12155.32, ISNI 0000 0001 0604 5662, Rehabilitation Research Center REVAL, , UHasselt, ; Hasselt, Belgium
                [3 ]GRID grid.491865.7, ISNI 0000 0001 0338 671X, Clinical and Cognitive Neurorehabilitation, Center of Neurology and Neurorehabilitation, , Klinik Bavaria Kreischa, ; An der Wolfsschlucht 1-2, 01703 Kreischa, Germany
                [4 ]GRID grid.7841.a, Department of Psychology, , Sapienza University of Rome, ; Rome, Italy
                [5 ]GRID grid.417778.a, ISNI 0000 0001 0692 3437, Ataxia Laboratory, , IRCCS Fondazione Santa Lucia, ; Rome, Italy
                [6 ]GRID grid.413871.8, ISNI 0000 0001 0124 3248, Department of Neurology, , CHU-Charleroi, ; 6000 Charleroi, Belgium
                [7 ]GRID grid.8364.9, ISNI 0000 0001 2184 581X, Department of Neurosciences, , University of Mons, ; 7000 Mons, Belgium
                [8 ]GRID grid.417778.a, ISNI 0000 0001 0692 3437, SPInal REhabilitation Lab (SPIRE), , IRCCS Fondazione Santa Lucia, ; Via Ardeatina 306, 00179 Rome, Italy
                [9 ]GRID grid.417778.a, ISNI 0000 0001 0692 3437, Neuro-Robot Rehabilitation Lab, , IRCCS Fondazione Santa Lucia, ; Via Ardeatina 306, 00179 Rome, Italy
                [10 ]GRID grid.63124.32, ISNI 0000 0001 2173 2321, Department of Psychology, , American University, ; Washington, DC 20016 USA
                [11 ]GRID grid.8767.e, ISNI 0000 0001 2290 8069, Department of Psychology, , Vrije Universiteit Brussel, ; Brussels, Belgium
                [12 ]GRID grid.47840.3f, ISNI 0000 0001 2181 7878, Department of Psychology, , University of California, ; Berkeley, CA USA
                [13 ]GRID grid.38142.3c, ISNI 000000041936754X, Ataxia Unit, Cognitive Behavioral Neurology Unit, Laboratory for Neuroanatomy and Cerebellar Neurobiology, Department of Neurology Massachusetts General Hospital, , Harvard Medical School, ; Boston, MA USA
                Author information
                http://orcid.org/0000-0001-8267-6861
                http://orcid.org/0000-0002-5212-8650
                http://orcid.org/0000-0003-3750-2760
                http://orcid.org/0000-0001-6034-4380
                http://orcid.org/0000-0003-1368-7692
                http://orcid.org/0000-0001-9808-9688
                http://orcid.org/0000-0003-2629-0213
                http://orcid.org/0000-0002-2538-9847
                http://orcid.org/0000-0003-0706-5125
                Article
                1068
                10.1007/s12311-019-01068-8
                6978293
                31522332
                ac685899-d12b-4723-a7ac-603ab605a382
                © The Author(s) 2019

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: NS105839
                Award ID: R15MH106957
                Award ID: R21DC014087
                Award Recipient :
                Funded by: Italian Ministry of Instruction, University and Research (MIUR)
                Award ID: RM11715C7E67E525
                Award Recipient :
                Funded by: Italian Ministry of Health (Ricerca Corrente)
                Award ID: -
                Award Recipient :
                Funded by: Ricerca Finalizzata of the Italian Ministry of Health
                Award ID: RF-2011-02348213
                Award Recipient :
                Funded by: NIH-NINDS
                Award ID: -
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100002243, National Ataxia Foundation;
                Award ID: -
                Award Recipient :
                Funded by: Ataxia Telangiectasia Children's Project
                Award ID: -
                Award Recipient :
                Funded by: MINDlink Foundation
                Award ID: -
                Award Recipient :
                Funded by: Strategic Research Program
                Award ID: SRP15
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                © Springer Science+Business Media, LLC, part of Springer Nature 2020

                Neurology
                cerebellum,cognition,emotion,affect,cerebellar cognitive affective syndrome,schmahmann syndrome

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