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

Author:

Wang Xinyi1ORCID,St George Rebecca J12,Bai Quan3,Tran Son3,Alty Jane1456

Affiliation:

1. Wicking Dementia Research and Education Centre , College of Health and Medicine, University of Tasmania, Hobart 7001 , Australia

2. School of Psychological Sciences , College of Health and Medicine, University of Tasmania, Hobart 7005 , Australia

3. Department of Information and Communication Technology , College of Science and Engineering, Hobart 7005 , Australia

4. School of Medicine , College of Health and Medicine, University of Tasmania, Hobart 7001 , Australia

5. Department of Neurology , Royal Hobart Hospital, Tasmania, Hobart 7001 , Australia

6. Department of Neurology , Leeds Teaching Hospitals NHS Trust, Leeds LS1 3EX , UK

Abstract

Abstract 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.

Funder

National Health and Medical Research Council

University of Tasmania

Wicking Trust

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Aging,General Medicine

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