Brain-first forms of Parkinson′s Disease are over-represented in patients with non-responsive resting tremor

Marcelo Mendonça, Pedro Ferreira, Raquel Barbosa, Joaquim Alves Da Silva
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Abstract

Motor subtypes in Parkinson′s Disease (PD) are unstable over time, limiting mechanistic insights and biomarker discovery. We focused on Rest Tremor (RT) as a symptom to test for phenotype stability and link them to specific circuits and disease mechanisms. Using the PPMI cohort data over 5 years we found that RT we found that RT is more stable than common Tremor- Dominant definitions, a stability also seen for therapy response. At time of diagnosis, the population of therapy-resistant RT patients was enriched with a brain-first PD profile as predicted by a-Synuclein origin site and connectome (SOC) model. Resistant-RT patients have lower gastrointestinal and cardiovascular symptoms, lower prevalence of probable REM-Sleep behavior disorder, and higher dopaminergic asymmetry compared to therapy-responsive or no tremor patients. Treating RT as a distinct phenomenon revealed a relative phenotypic stability with treatment response being linked to different patterns of disease progression.
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无反应静止性震颤患者中脑先兆帕金森病的比例过高
帕金森病(Parkinson′s Disease,PD)的运动亚型随着时间的推移不稳定,限制了机理认识和生物标志物的发现。我们将静息震颤(RT)作为一种症状来测试表型的稳定性,并将其与特定回路和疾病机制联系起来。利用 PPMIcohort 5 年来的数据,我们发现 RT 比常见的震颤主导型定义更稳定,这种稳定性也体现在治疗反应上。在确诊时,治疗耐药的 RT 患者群富含 a-Synuclein 起源部位和连接组(SOC)模型预测的脑先天性震颤症特征。与治疗应答型或无震颤型患者相比,治疗应答型 RT 患者的胃肠道和心血管症状较轻,可能的快速动眼期睡眠行为障碍发生率较低,多巴胺能不对称程度较高。将震颤作为一种独特的现象来处理,会发现其表型具有相对的稳定性,治疗反应与疾病进展的不同模式有关。
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