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Reclassification of patients with tremor syndrome and comparisons of essential tremor and essential tremor-plus patients

原发性震颤 医学 队列 神经学 萧条(经济学) 焦虑 生活质量(医疗保健) 神经组阅片室 物理疗法 运动障碍 儿科 物理医学与康复
作者
Jiaxin Peng,Nan-Nan Li,Jun-Ying Li,Li-Ren Duan,Chaolan Chen,Yan Zeng,Jing Xi,Yi Jiang,Rong Peng
出处
期刊:Journal of Neurology [Springer Science+Business Media]
标识
DOI:10.1007/s00415-022-10985-4
摘要

The new essential tremor (ET)-plus nomenclature was proposed by the 2018 Tremor Consensus Criteria. However, few studies have adopted this usage and the clinical differences between ET and ET-plus remains unclear. To address this issue, we reclassified and compared the characteristics of ET and ET-plus patients in a large Chinese tremor cohort.In this cross-sectional observational study, 766 patients originally diagnosed with ET underwent neurological examination. Scale ratings were used to evaluate motor and non-motor symptoms, and quality of life (QoL). We then reclassified the ET cohort and compared demographic and clinical characteristics between ET and ET-plus patients. A logistic regression analysis was used to explore whether the presence of neurological soft signs in ET-plus was associated with tremor severity or QoL.Among 665 clinically confirmed ET syndrome patients, 274 were ET and 391 were ET-plus. The most prevalent neurological soft sign was resting tremor. ET-plus patients were older, had older age at onset and longer disease duration. ET-plus patients recorded higher scores in tremor severity evaluations and lower in cognitive evaluations, whereas a higher proportion of patients presented with depression or anxiety symptoms. Resting tremor and questionable cerebellar signs were associated with tremor severity. Cognitive impairment was associated with worse QoL.ET-plus patients were older, had longer disease durations, worse tremor manifestations, and more distinct non-motor symptoms. Certain additional soft signs of ET-plus were associated with tremor severity or worse QoL. ET-plus patients may include advanced ET patients with additional neurological soft signs presenting along with disease progression.
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