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      Diagnostic Criteria for Dementia with Lewy Bodies: Updates and Future Directions

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          Abstract

          The aim of this article is to describe the 2017 revised consensus criteria for the clinical diagnosis of dementia with Lewy bodies (DLB) with future directions for the diagnostic criteria. The criteria for the clinical diagnosis of probable and possible DLB were first published as the first consensus report in 1996 and were revised in the third consensus report in 2005. After discussion at the International DLB Conference in Fort Lauderdale, Florida, USA, in 2015, the International DLB Consortium published the fourth consensus report including the revised consensus criteria in 2017. The 2017 revised criteria clearly distinguish between clinical features and diagnostic biomarkers. Significant new information about previously reported aspects of DLB has been incorporated, with increased diagnostic weighting given to rapid eye movement (REM) sleep behavior disorder (RBD) and iodine-123-metaiodobenzylguanidine (MIBG) myocardial scintigraphy. Future directions include the development of the criteria for early diagnosis (prodromal DLB) and the establishment of new biomarkers that directly indicate Lewy-related pathology, including α-synuclein imaging, biopsies of peripheral tissues (skin, etc.) for the demonstration of α-synuclein deposition, and biochemical markers (cerebrospinal fluid/blood), as well as the pathological evaluation of the sensitivity and specificity of the 2017 revised diagnostic criteria. In conclusion, the revised consensus criteria for the clinical diagnosis of DLB were reported with the incorporation of new information about DLB in 2017. Future directions include the development of the criteria for early diagnosis and the establishment of biomarkers directly indicative of Lewy-related pathology.

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          Most cited references36

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          Neuropathological and genetic correlates of survival and dementia onset in synucleinopathies: a retrospective analysis.

          Great heterogeneity exists in survival and the interval between onset of motor symptoms and dementia symptoms across synucleinopathies. We aimed to identify genetic and pathological markers that have the strongest association with these features of clinical heterogeneity in synucleinopathies.
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            Induction of α-synuclein aggregate formation by CSF exosomes from patients with Parkinson’s disease and dementia with Lewy bodies

            Stuendl et al. show that CSF exosomes of patients with Parkinson’s disease or dementia with Lewy bodies contain α-synuclein and induce α-synuclein aggregation in a reporter cell line. Thus, exosomes may support inter-neuronal transmission of α-synuclein pathology. CSF exosomal α-synuclein may serve as a biomarker in α-synuclein-related neurodegeneration.
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              Pathological alpha-synuclein propagates through neural networks

              Background α-Synuclein is the major component of filamentous inclusions that constitute the defining characteristic of Parkinson’s disease, dementia with Lewy bodies and multiple system atrophy, so-called α-synucleinopathies. Recent studies revealed that intracerebral injection of recombinant α-synuclein fibrils into wild-type mouse brains induced prion-like propagation of hyperphosphorylated α-synuclein pathology. However, the propagation mechanisms of α-synuclein have not been fully elucidated. Results In this study, in order to establish where and how α-synuclein pathology propagates, we injected recombinant mouse α-synuclein fibrils into three different brain areas (substantia nigra, striatum, and entorhinal cortex) of wild-type mice and compared the resulting distributions of α-synuclein pathology at 1 month after injection. Distinct patterns of pathology were observed in mice injected at the different sites. Within one month after injection, the pathology had spread to neurons in areas far from the injection sites, especially areas with direct neural connections to the injection sites. Surprisingly, phosphorylated tau and TDP-43 pathologies were also observed in mice injected with α-synuclein fibrils into striatum and entorhinal cortex at one month after injection. Phosphorylated tau and TDP-43 were accumulated in dot-like inclusions, but these were rarely colocalized with α-synuclein pathology. It seems that accumulation of α-synuclein has a synergistic effect on tau and TDP-43 aggregation. Additionally, intracerebral injection with sarkosyl-insoluble fraction prepared from wild-type mice injected synthetic α-synuclein fibrils can also induce phosphorylated α-synuclein pathology in wild-type mice. Conclusions Our data indicate that α-synuclein aggregation spread by prion-like mechanisms through neural networks in mouse brains. Electronic supplementary material The online version of this article (doi:10.1186/s40478-014-0088-8) contains supplementary material, which is available to authorized users.
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                Author and article information

                Journal
                J Mov Disord
                J Mov Disord
                JMD
                Journal of Movement Disorders
                The Korean Movement Disorder Society
                2005-940X
                2093-4939
                January 2020
                8 November 2019
                : 13
                : 1
                : 1-10
                Affiliations
                [1 ]Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan
                [2 ]Department of Nuclear Medicine, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan
                [3 ]Department of Neurology, National Hospital Organization, Hokuriku National Hospital, Nanto, Japan
                Author notes
                Corresponding author: Masahito Yamada, MD, PhD Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Sciences, 13-1 Takara-machi, Kanazawa 920-8640, Japan / Tel: +81-76-265-2290 / Fax: +81-76-234-4253 / E-mail: m-yamada@ 123456med.kanazawa-u.ac.jp
                Author information
                http://orcid.org/0000-0003-2416-5662
                http://orcid.org/0000-0002-5150-6322
                http://orcid.org/0000-0003-4964-669X
                http://orcid.org/0000-0002-8865-4097
                http://orcid.org/0000-0002-6558-3919
                http://orcid.org/0000-0001-7188-8746
                http://orcid.org/0000-0001-5979-8385
                Article
                jmd-19052
                10.14802/jmd.19052
                6987529
                31694357
                6db2b606-076c-40ad-a73b-be27a8a9d0ff
                Copyright © 2020 The Korean Movement Disorder Society

                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 unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 6 July 2019
                : 13 August 2019
                : 6 September 2019
                Categories
                Review Article

                α-synuclein,clinical practice guideline,dementia,lewy body,myocardial scintigraphy

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