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迟发性特发性震颤的新视野:痴呆的认知前生物标志物?

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

机构信息

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

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

出版信息

Age Ageing. 2022 Jul 1;51(7). doi: 10.1093/ageing/afac135.

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.

摘要

特发性震颤(ET)是老年人震颤最常见的原因。然而,越来越多的人认识到,30-50%的 ET 病例被误诊。发病年龄在 60 岁以后的迟发性 ET 尤其容易被误诊,越来越多的证据表明它可能是一种独特的临床实体,或许更好地称为“与年龄相关的震颤”。与发病年龄较早的 ET 老年人相比,迟发性 ET 与握力减弱、认知能力下降、痴呆和死亡有关。这就提出了一些问题,即迟发性 ET 是否是痴呆的认知前生物标志物,以及是否可以在这组患者中特别重视改变痴呆风险因素。另一方面,迟发性 ET 的临床表现可能只是反映了健康衰老或脆弱的标志物,叠加在典型的 ET 上。这些问题需要澄清,尤其是在为老年人提供越来越多的专业神经外科治疗 ET 的时代,这些治疗方法可能不适合认知能力下降风险较高的人群。临床医生迫切需要了解迟发性 ET,但由于专门针对这一主题的出版物很少,且缺乏指导预后的特定特征,因此这具有一定的挑战性。更严格的临床随访和使用易于获取的计算机技术对迟发性 ET 的临床表现进行精确的表型分析,可能有助于我们确定迟发性 ET 是否是一种独立的临床实体,并有助于预后判断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8350/9249070/d237e6b71a63/afac135f1.jpg

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