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      Diagnosis and management of dementia with Lewy bodies : Fourth consensus report of the DLB Consortium

      review-article
      , MD, F Med Sci , , MD, , MD, , PhD, , PhD, MRC Psych, , MD, , MD, , MD, MPH, , MD, , MRC Psych, MD, , BA, LLB, , MD, PhD, , MD, PhD, , MD, PhD, , MD, PhD, , PhD, , MD, PhD, , MD, FRCP, , MD, , MD, , PhD, , MD, FRCP, , PhD, , MD, , MD, , MD, , MD, MS, , MD, PhD, , MD, , MD, PhD, , MD, PhD, , MD, MS, , MD, , PhD, , PhD, , MD, , MBBCh, MD, , MD, , MA, , MD, PhD, , MD, , PhD, , MD, , MD, PhD, , MD, PhD, , MD, PhD, , PhD,   , F Med Sci, DM, , MD, PhD, , MD, MSc, , MD, , PhD, , PhD, , PhD, , BM, , PhD, , MD, , MD, PhD, , MD, PhD, , MD, , MD, FRC Psych, , MD, PhD, , MD
      Neurology
      Lippincott Williams & Wilkins

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          Abstract

          The Dementia with Lewy Bodies (DLB) Consortium has refined its recommendations about the clinical and pathologic diagnosis of DLB, updating the previous report, which has been in widespread use for the last decade. The revised DLB consensus criteria now distinguish clearly between clinical features and diagnostic biomarkers, and give guidance about optimal methods to establish and interpret these. Substantial new information has been incorporated about previously reported aspects of DLB, with increased diagnostic weighting given to REM sleep behavior disorder and 123iodine-metaiodobenzylguanidine (MIBG) myocardial scintigraphy. The diagnostic role of other neuroimaging, electrophysiologic, and laboratory investigations is also described. Minor modifications to pathologic methods and criteria are recommended to take account of Alzheimer disease neuropathologic change, to add previously omitted Lewy-related pathology categories, and to include assessments for substantia nigra neuronal loss. Recommendations about clinical management are largely based upon expert opinion since randomized controlled trials in DLB are few. Substantial progress has been made since the previous report in the detection and recognition of DLB as a common and important clinical disorder. During that period it has been incorporated into DSM-5, as major neurocognitive disorder with Lewy bodies. There remains a pressing need to understand the underlying neurobiology and pathophysiology of DLB, to develop and deliver clinical trials with both symptomatic and disease-modifying agents, and to help patients and carers worldwide to inform themselves about the disease, its prognosis, best available treatments, ongoing research, and how to get adequate support.

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          Most cited references36

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          The Clinician Assessment of Fluctuation and the One Day Fluctuation Assessment Scale. Two methods to assess fluctuating confusion in dementia.

          The identification of fluctuating confusion is central to improving the differential diagnosis of the common dementias. To determine the value of two rating scales to measure fluctuating confusion. The agreement between the clinician-rated scale and the scale completed by a non-clinician was determined. Correlations between the two scales were calculated; variability in attention was calculated on a computerised cognitive assessment and variability in delta rhythm on an electroencephalogram (EEG). The Clinician Assessment of Fluctuation and the computerised cognitive assessment were completed for 155 patients (61 Alzheimer's disease, 37 dementia with Lewy bodies, 22 vascular dementia, 35 elderly controls). A subgroup (n = 40) received a further evaluation using the One Day Fluctuation Assessment Scale and an EEG. The two scales correlated significantly with each other, and with the neuropsychological and electrophysiological measures of fluctuation. Both scales are useful instruments for the clinical assessment of fluctuation in dementia.
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            Neurodegenerative Disorder Risk in Idiopathic REM Sleep Behavior Disorder: Study in 174 Patients

            Objective To estimate the risk for developing a defined neurodegenerative syndrome in a large cohort of idiopathic REM sleep behavior disorder (IRBD) patients with long follow-up. Methods Using the Kaplan-Meier method, we estimated the disease-free survival rate from defined neurodegenerative syndromes in all the consecutive IRBD patients diagnosed and followed-up in our tertiary referal sleep center between November 1991 and July 2013. Results The cohort comprises 174 patients with a median age at diagnosis of IRBD of 69 years and a median follow-up of four years. The risk of a defined neurodegenerative syndrome from the time of IRBD diagnosis was 33.1% at five years, 75.7% at ten years, and 90.9% at 14 years. The median conversion time was 7.5 years. Emerging diagnoses (37.4%) were dementia with Lewy bodies (DLB) in 29 subjects, Parkinson disease (PD) in 22, multiple system atrophy (MSA) in two, and mild cognitive impairment (MCI) in 12. In six cases, in whom postmortem was performed, neuropathological examination disclosed neuronal loss and widespread Lewy-type pathology in the brain in each case. Conclusions In a large IRBD cohort diagnosed in a tertiary referal sleep center, prolonged follow-up indicated that the majority of patients are eventually diagnosed with the synucleinopathies PD, DLB and less frequently MSA. IRBD represented the prodromal period of these conditions. Our findings in IRBD have important implications in clinical practice, in the investigation of the early pathological events occurring in the synucleinopathies, and for the design of interventions with potential disease-modifying agents.
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              Clinicopathologic correlations in 172 cases of rapid eye movement sleep behavior disorder with or without a coexisting neurologic disorder.

              To determine the pathologic substrates in patients with rapid eye movement (REM) sleep behavior disorder (RBD) with or without a coexisting neurologic disorder.
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                Author and article information

                Contributors
                Journal
                Neurology
                Neurology
                neurology
                neur
                neurology
                NEUROLOGY
                Neurology
                Lippincott Williams & Wilkins (Hagerstown, MD )
                0028-3878
                1526-632X
                04 July 2017
                04 July 2017
                : 89
                : 1
                : 88-100
                Affiliations
                Author affiliations are provided at the end of the article.
                Author notes
                Correspondence to Dr. McKeith: ian.mckeith@ 123456newcastle.ac.uk

                Members of the DLB Consortium are listed at Neurology.org.

                Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article. The Article Processing Charge was paid by NIHR Newcastle Biomedical Research Centre in Ageing and Long-Term Conditions.

                Article
                NEUROLOGY2016770735
                10.1212/WNL.0000000000004058
                5496518
                28592453
                5a86fe51-052e-47c1-872e-dafb76c61592
                Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.

                This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 30 September 2016
                : 30 March 2017
                Funding
                Funded by: NIH
                Award ID: R13 NS095618, P50-NS072187, P01-AG003949, P50-AG016574, RO1 NS082265, UO1 NS082134, and P50 NS053488
                Funded by: NINDS
                Award ID: P50 NS072187 and R01 NS078086
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