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Challenges in Predicting Cognitive Decline in Dementia with Lewy Bodies

Research output: Contribution to journalReview articlepeer-review

Konstantinos Tsamakis, Christoph Mueller

Original languageEnglish
Pages (from-to)1-8
Number of pages8
JournalDementia and Geriatric Cognitive Disorders
Volume50
Issue number1
DOIs
Accepted/In press2021
Published1 Jun 2021

Bibliographical note

Funding Information: C.M. receives salary support from the National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley N.H.S. Foundation Trust and King’s College London. The views expressed are those of the author(s) and not necessarily those of the N.H.S., the NIHR, or the Department of Health and Social Care. Funding Information: C.M. receives salary support from the National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley N.H.S. Foundation Trust and King's College London. The views expressed are those of the author(s) and not necessarily those of the N.H.S., the NIHR, or the Department of Health and Social Care Publisher Copyright: © 2021 The Author(s) Published by S. Karger AG, Basel. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.

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Abstract

Despite being the second most common form of neurodegenerative dementia, dementia with Lewy bodies (DLB) is underrecognized and carries a worse prognosis than other subtypes of the condition. Cognitive impairment is a cardi- nal feature of all types of dementia and DLB presents with a distinct profile with deficits in attention, executive function, and visuoperceptual abilities. This difference from Alzheimer’s disease and the common presence of neuropsychiatric symptoms may lead to challenges in predicting cognitive decline in this patient population. Firstly, the diagnosis of DLB is often delayed in clinical practice leading to variability from which time point in the disease course cognitive decline is measured. Secondly, the most frequently used measurement tools for cognitive difficulties focus on memory and naming rather than the domains affected by DLB. While there is now largely a consensus which tools are useful in diagnosing DLB, their validity in assessing deteriorating cognition is less clear. Thirdly, the presence of fluctuating cogni- tion, the propensity to develop delirium episodes, as well as difficulties in distinguishing the two entities in clinical practice make it difficult to predict the disease course. Sleep disturbances are likely to influence cognitive decline but require further study in patients within established DLB. Fourthly, as in most cases of dementia, neuropathological comorbidities are frequently present in DLB. While the influence of Alzheimer’s pathology on cognitive decline in DLB is comparatively well understood, the impact of other pathologies remains unclear. The recent definition of research criteria for mild cognitive impairment in DLB could facilitate earlier diagnosis and more structured follow-up. Assessment tools measuring cognitive domains predominantly affected in DLB need to be more consistently used in longitudinal studies and clinical practice, as well as concurrent measures of fluctuations in cognition. Greater availability of biomarkers and digital healthcare solutions can play an important role in enabling more accurate monitoring and prediction of cognitive decline in DLB.

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