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      Locus coeruleus imaging as a biomarker for noradrenergic dysfunction in neurodegenerative diseases

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      Brain
      Oxford University Press
      locus coeruleus (LC), magnetic resonance imaging (MRI), neurodegeneration, noradrenaline (NA) biomarker

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          Abstract

          The locus coeruleus is the site of the earliest pathological changes in many neurodegenerative diseases. Betts et al. describe how in vivo locus coeruleus imaging can be used as a biomarker for noradrenergic dysfunction in neurodegenerative diseases, and outline a strategy for achieving reliable and biologically validated imaging approaches.

          Abstract

          Pathological alterations to the locus coeruleus, the major source of noradrenaline in the brain, are histologically evident in early stages of neurodegenerative diseases. Novel MRI approaches now provide an opportunity to quantify structural features of the locus coeruleus in vivo during disease progression. In combination with neuropathological biomarkers, in vivo locus coeruleus imaging could help to understand the contribution of locus coeruleus neurodegeneration to clinical and pathological manifestations in Alzheimer’s disease, atypical neurodegenerative dementias and Parkinson’s disease. Moreover, as the functional sensitivity of the noradrenergic system is likely to change with disease progression, in vivo measures of locus coeruleus integrity could provide new pathophysiological insights into cognitive and behavioural symptoms. Locus coeruleus imaging also holds the promise to stratify patients into clinical trials according to noradrenergic dysfunction. In this article, we present a consensus on how non-invasive in vivo assessment of locus coeruleus integrity can be used for clinical research in neurodegenerative diseases. We outline the next steps for in vivo, post-mortem and clinical studies that can lay the groundwork to evaluate the potential of locus coeruleus imaging as a biomarker for neurodegenerative diseases.

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          Most cited references115

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          Stages in the development of Parkinson's disease-related pathology.

          The synucleinopathy, idiopathic Parkinson's disease, is a multisystem disorder that involves only a few predisposed nerve cell types in specific regions of the human nervous system. The intracerebral formation of abnormal proteinaceous Lewy bodies and Lewy neurites begins at defined induction sites and advances in a topographically predictable sequence. As the disease progresses, components of the autonomic, limbic, and somatomotor systems become particularly badly damaged. During presymptomatic stages 1-2, inclusion body pathology is confined to the medulla oblongata/pontine tegmentum and olfactory bulb/anterior olfactory nucleus. In stages 3-4, the substantia nigra and other nuclear grays of the midbrain and forebrain become the focus of initially slight and, then, severe pathological changes. At this point, most individuals probably cross the threshold to the symptomatic phase of the illness. In the end-stages 5-6, the process enters the mature neocortex, and the disease manifests itself in all of its clinical dimensions.
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            Activity of norepinephrine-containing locus coeruleus neurons in behaving rats anticipates fluctuations in the sleep-waking cycle.

            Spontaneous discharge of norepinephrine-containing locus coeruleus (NE-LC) neurons was examined during the sleep-walking cycle (S-WC) in behaving rats. Single unit and multiple unit extracellular recordings yielded a consistent set of characteristic discharge properties. (1) Tonic discharge co-varied with stages of the S-WC, being highest during waking, lower during slow wave sleep, and virtually absent during paradoxical sleep. (2) Discharge anticipated S-WC stages as well as phasic cortical activity, such as spindles, during slow wave sleep. (3) Discharge decreased within active waking during grooming and sweet water consumption. (4) Bursts of impulses accompanied spontaneous or sensory-evoked interruptions of sleep, grooming, consumption, or other such ongoing behavior. (5) These characteristic discharge properties were topographically homogeneous for recordings throughout the NE-LC. (6) Phasic robust activity was synchronized markedly among neurons in multiple unit populations. (7) Field potentials occurred spontaneously in the NE-LC and were synchronized with bursts of unit activity from the same electrodes. (8) Field potentials became dissociated from unit activity during paradoxical sleep, exhibiting their highest rates in the virtual absence of impulses. These results are generally consistent with previous proposals that the NE-LC system is involved in regulating cortical and behavioral arousal. On the basis of the present data and those described in the following report (Aston-Jones, G., and F. E. Bloom (1981) J. Neurosci.1: 887-900), we conclude that these neurons may mediate a specific function within the general arousal framework. In brief, the NE-LC system may globally bias the responsiveness of target neurons and thereby influence overall behavioral orientation.
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              The locus coeruleus-noradrenergic system: modulation of behavioral state and state-dependent cognitive processes.

              Through a widespread efferent projection system, the locus coeruleus-noradrenergic system supplies norepinephrine throughout the central nervous system. Initial studies provided critical insight into the basic organization and properties of this system. More recent work identifies a complicated array of behavioral and electrophysiological actions that have in common the facilitation of processing of relevant, or salient, information. This involves two basic levels of action. First, the system contributes to the initiation and maintenance of behavioral and forebrain neuronal activity states appropriate for the collection of sensory information (e.g. waking). Second, within the waking state, this system modulates the collection and processing of salient sensory information through a diversity of concentration-dependent actions within cortical and subcortical sensory, attention, and memory circuits. Norepinephrine-dependent modulation of long-term alterations in synaptic strength, gene transcription and other processes suggest a potentially critical role of this neurotransmitter system in experience-dependent alterations in neural function and behavior. The ability of a given stimulus to increase locus coeruleus discharge activity appears independent of affective valence (appetitive vs. aversive). Combined, these observations suggest that the locus coeruleus-noradrenergic system is a critical component of the neural architecture supporting interaction with, and navigation through, a complex world. These observations further suggest that dysregulation of locus coeruleus-noradrenergic neurotransmission may contribute to cognitive and/or arousal dysfunction associated with a variety of psychiatric disorders, including attention-deficit hyperactivity disorder, sleep and arousal disorders, as well as certain affective disorders, including post-traumatic stress disorder. Independent of an etiological role in these disorders, the locus coeruleus-noradrenergic system represents an appropriate target for pharmacological treatment of specific attention, memory and/or arousal dysfunction associated with a variety of behavioral/cognitive disorders.
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                Author and article information

                Journal
                Brain
                Brain
                brainj
                Brain
                Oxford University Press
                0006-8950
                1460-2156
                September 2019
                20 July 2019
                20 July 2019
                : 142
                : 9
                : 2558-2571
                Affiliations
                [1 ]German Center for Neurodegenerative Diseases (DZNE), Magdeburg, Germany
                [2 ]Institute of Cognitive Neurology and Dementia Research, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany
                [3 ]Department of Neurophysics, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany
                [4 ]Center for Cognitive Neuroscience, Free University Berlin, Berlin, Germany
                [5 ]Laboratory of Magnetic Resonance LIM44, Department and Institute of Radiology, Medical School of the University of São Paulo, Brazil
                [6 ]Department of Cognitive Neuroscience, Faculty of Psychology and Neuroscience, Maastricht University, MD, Maastricht, The Netherlands
                [7 ]Wellcome Centre for Human Neuroimaging, UCL Institute of Neurology, London, UK
                [8 ]Department of Clinical Neurosciences, University of Cambridge, UK
                [9 ]Consiglio Nazionale delle Ricerche, Istituto di Bioimmagini e Fisiologia Molecolare (IBFM), Milan, Italy
                [10 ]Institute of Cognitive Neuroscience, University College London, London, UK
                [11 ]University of Amsterdam, Integrative Model-based Cognitive Neuroscience research unit, Amsterdam, The Netherlands
                [12 ]University of Leiden, Cognitive Psychology, Leiden, The Netherlands
                [13 ]Department of Neurology, Vanderbilt University Medical Center, Nashville, TN, USA
                [14 ]Department of Biomedical Magnetic Resonance, Institute for Physics, Otto-von-Guericke-University, Magdeburg, Germany
                [15 ]Department of Neurology, Otto-von-Guericke University, Magdeburg, Germany
                [16 ]Division of Psychiatry, University College London, London, UK
                [17 ]Faculty of Health, Medicine and Life Sciences, School for Mental Health and Neuroscience, Alzheimer Centre Limburg, Maastricht University, Maastricht, The Netherlands
                [18 ]Department for Neurodegenerative Diseases and Geriatric Psychiatry, University Hospital Bonn, Bonn, Germany
                [19 ]German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany
                [20 ]Center for Lifespan Psychology, Max Planck Institute for Human Development, Berlin, Germany
                [21 ]Danish Research Centre for Magnetic Resonance, Centre for Functional and Diagnostic Imaging and Research, Copenhagen University Hospital Hvidovre, Denmark
                [22 ]Memory and Aging Center, Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA
                [23 ]Department of Integrative Biology, University of California, Berkeley, Berkeley, CA, USA
                [24 ]Center for Behavioral Brain Sciences, Magdeburg, Germany
                [25 ]Leibniz Institute for Neurobiology, Magdeburg, Germany
                [26 ]Max Planck Centre for Computational Psychiatry and Ageing, University College London, UK
                [27 ]Henry H. Wheeler, Jr. Brain Imaging Center, University of California, Berkeley, CA, USA
                [28 ]Department of Radiology and Biomedical Imaging, University of California - San Francisco, San Francisco, CA, USA
                [29 ]Paul Flechsig Institute of Brain Research, Medical Faculty, University of Leipzig, Leipzig, Germany
                [30 ]Institute of Biomedical Technologies, National Research Council of Italy, Segrate, Milan, Italy
                [31 ]Leonard Davis School of Gerontology and Department of Psychology, University of Southern California, Los Angeles, CA, USA
                [32 ]Centre for Neuroscience Imaging Research, Institute for Basic Science and Department of Biomedical Engineering, Sungkyunkwan University, Suwon, Republic of Korea
                [33 ]Techna Institute and Koerner Scientist in MR Imaging, University Health Network, Toronto, Canada
                [34 ]University of São Paulo Medical School, São Paulo, Brazil
                [35 ]Clinic of Psychiatry, University of Würzburg, Wurzburg, Germany
                [36 ]Department of Psychiatry, Columbia University Medical Center, New York State Psychiatric Institute, New York, USA
                [37 ]Global Brain Health Institute, University of California, San Francisco, San Francisco, CA, USA
                [38 ]Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA
                [39 ]Faculty of Health, Medicine and Life Sciences, School for Mental Health and Neuroscience, Alzheimer Centre Limburg, Maastricht University, Maastricht, The Netherlands
                Author notes
                Correspondence to: Matthew J. Betts German Center for Neurodegenerative Diseases (DZNE) Magdeburg, Germany E-mail: matthew.betts@ 123456dzne.de

                Emrah Düzel and Dorothea Hämmerer authors contributed equally to this work.

                Article
                awz193
                10.1093/brain/awz193
                6736046
                31327002
                a6f46d2f-1a2e-440d-afe0-4a5191d6b824
                © The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 22 February 2019
                : 12 April 2019
                : 1 May 2019
                Page count
                Pages: 14
                Funding
                Funded by: Human Brain Project
                Award ID: SP3 WP 3.3.1
                Funded by: MRC 10.13039/501100000265
                Award ID: MR/P012698/1
                Funded by: Italian Ministry of Education, University,and Research
                Funded by: MIUR 10.13039/501100003407
                Funded by: National Research Programme
                Funded by: PNR
                Funded by: National Research Council of Italy
                Funded by: CNR 10.13039/100008245
                Funded by: Flagship “InterOmics” Project
                Funded by: Grigioni Foundation for Parkinson's Disease
                Funded by: MRC 10.13039/501100000265
                Award ID: MR/R006504/1
                Funded by: MRC 10.13039/501100000265
                Award ID: MR/P01271X/1
                Funded by: MRC 10.13039/501100000265
                Funded by: NIHR 10.13039/100006662
                Funded by: Wellcome Trust 10.13039/100004440
                Award ID: 103838
                Funded by: McDonnell Foundation 10.13039/100000913
                Funded by: AZ-Medimmune
                Funded by: Janssen
                Funded by: German Research Foundation 10.13039/501100001659
                Funded by: DFG 10.13039/100004807
                Funded by: NWO VENI
                Funded by: Alzheimer Nederland 10.13039/501100010969
                Funded by: European Union's Horizon 2020 Research and Innovation Programme
                Award ID: IF-2015-GF, 706714
                Funded by: European Research Council 10.13039/100010663
                Award ID: FP7/2007-2013
                Award ID: 681094
                Funded by: BMBF 10.13039/501100002347
                Award ID: 01EW1711A
                Funded by: Lundbeck Foundation 10.13039/501100003554
                Award ID: R186-2015-2138
                Funded by: NIH 10.13039/100000002
                Award ID: R01AG056573
                Award ID: K24AG053435
                Funded by: BrightFocus Foundation 10.13039/100006312
                Funded by: UCLH 10.13039/501100008721
                Funded by: NIHR Biomedical Research Centre
                Funded by: German Research Foundation 10.13039/501100001659
                Funded by: DFG 10.13039/100004807
                Funded by: Wellcome Centre for Human Neuroimaging
                Funded by: Wellcome 10.13039/100004440
                Award ID: 203147/Z/16/Z
                Categories
                Update

                Neurosciences
                locus coeruleus (lc),magnetic resonance imaging (mri),neurodegeneration,noradrenaline (na) biomarker

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