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New horizons in late-onset essential tremor: a pre-cognitive biomarker of dementia?

Essential tremor (ET) is the most common cause of tremor in older adults. However, it is increasingly recognised that 30–50% of ET cases are misdiagnosed. Late-onset ET, when tremor begins after the age of 60, is particularly likely to be misdiagnosed and there is mounting evidence that it may be a...

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Autores principales: Wang, Xinyi, St George, Rebecca J, Bai, Quan, Tran, Son, Alty, Jane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249070/
https://www.ncbi.nlm.nih.gov/pubmed/35776673
http://dx.doi.org/10.1093/ageing/afac135
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author Wang, Xinyi
St George, Rebecca J
Bai, Quan
Tran, Son
Alty, Jane
author_facet Wang, Xinyi
St George, Rebecca J
Bai, Quan
Tran, Son
Alty, Jane
author_sort Wang, Xinyi
collection PubMed
description Essential tremor (ET) is the most common cause of tremor in older adults. However, it is increasingly recognised that 30–50% of ET cases are misdiagnosed. Late-onset ET, when tremor begins after the age of 60, is particularly likely to be misdiagnosed and there is mounting evidence that it may be a distinct clinical entity, perhaps better termed ‘ageing-related tremor’. Compared with older adults with early-onset ET, late-onset ET is associated with weak grip strength, cognitive decline, dementia and mortality. This raises questions around whether late-onset ET is a pre-cognitive biomarker of dementia and whether modification of dementia risk factors may be particularly important in this group. On the other hand, it is possible that the clinical manifestations of late-onset ET simply reflect markers of healthy ageing, or frailty, superimposed on typical ET. These issues are important to clarify, especially in the era of specialist neurosurgical treatments for ET being increasingly offered to older adults, and these may not be suitable in people at high risk of cognitive decline. There is a pressing need for clinicians to understand late-onset ET, but this is challenging when there are so few publications specifically focussed on this subject and no specific features to guide prognosis. More rigorous clinical follow-up and precise phenotyping of the clinical manifestations of late-onset ET using accessible computer technologies may help us delineate whether late-onset ET is a separate clinical entity and aid prognostication.
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spelling pubmed-92490702022-07-05 New horizons in late-onset essential tremor: a pre-cognitive biomarker of dementia? Wang, Xinyi St George, Rebecca J Bai, Quan Tran, Son Alty, Jane Age Ageing New Horizons Essential tremor (ET) is the most common cause of tremor in older adults. However, it is increasingly recognised that 30–50% of ET cases are misdiagnosed. Late-onset ET, when tremor begins after the age of 60, is particularly likely to be misdiagnosed and there is mounting evidence that it may be a distinct clinical entity, perhaps better termed ‘ageing-related tremor’. Compared with older adults with early-onset ET, late-onset ET is associated with weak grip strength, cognitive decline, dementia and mortality. This raises questions around whether late-onset ET is a pre-cognitive biomarker of dementia and whether modification of dementia risk factors may be particularly important in this group. On the other hand, it is possible that the clinical manifestations of late-onset ET simply reflect markers of healthy ageing, or frailty, superimposed on typical ET. These issues are important to clarify, especially in the era of specialist neurosurgical treatments for ET being increasingly offered to older adults, and these may not be suitable in people at high risk of cognitive decline. There is a pressing need for clinicians to understand late-onset ET, but this is challenging when there are so few publications specifically focussed on this subject and no specific features to guide prognosis. More rigorous clinical follow-up and precise phenotyping of the clinical manifestations of late-onset ET using accessible computer technologies may help us delineate whether late-onset ET is a separate clinical entity and aid prognostication. Oxford University Press 2022-07-01 /pmc/articles/PMC9249070/ /pubmed/35776673 http://dx.doi.org/10.1093/ageing/afac135 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the British Geriatrics Society. All rights reserved. For permissions, please email: journals.permissions@oup.com https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://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
spellingShingle New Horizons
Wang, Xinyi
St George, Rebecca J
Bai, Quan
Tran, Son
Alty, Jane
New horizons in late-onset essential tremor: a pre-cognitive biomarker of dementia?
title New horizons in late-onset essential tremor: a pre-cognitive biomarker of dementia?
title_full New horizons in late-onset essential tremor: a pre-cognitive biomarker of dementia?
title_fullStr New horizons in late-onset essential tremor: a pre-cognitive biomarker of dementia?
title_full_unstemmed New horizons in late-onset essential tremor: a pre-cognitive biomarker of dementia?
title_short New horizons in late-onset essential tremor: a pre-cognitive biomarker of dementia?
title_sort new horizons in late-onset essential tremor: a pre-cognitive biomarker of dementia?
topic New Horizons
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249070/
https://www.ncbi.nlm.nih.gov/pubmed/35776673
http://dx.doi.org/10.1093/ageing/afac135
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