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帕金森病发病年龄对症状谱、治疗特征和健康相关生活质量的影响。

Impact of age at onset on symptom profiles, treatment characteristics and health-related quality of life in Parkinson's disease.

机构信息

H. Lundbeck A/S, Valby, Denmark.

Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Lund, Sweden.

出版信息

Sci Rep. 2022 Jan 11;12(1):526. doi: 10.1038/s41598-021-04356-8.

Abstract

Parkinson's disease (PD) is typically considered an age-related disease, but the age at disease onset can vary by decades between patients. Aging and aging-associated diseases can affect the movement system independently of PD, and advanced age has previously been proposed to be associated with a more severe PD phenotype with accelerated progression. In this work, we investigated how interactions between PD progression and aging affect a wide range of outcomes related to PD motor and nonmotor symptoms as well as Health Related Quality of Life (HRQoL) and treatment characteristics. This population-based cohort study is based on 1436 PD patients from southern Sweden followed longitudinally for up to approximately 7.5 years from enrollment (3470 visits covering 2285 patient years, average follow-up time 1.7 years). Higher age at onset was generally associated with faster progression of motor symptoms, with a notable exception of dyskinesia and other levodopa-associated motor fluctuations that had less severe trajectories for patients with higher age at onset. Mixed results were observed for emergence of non-motor symptoms, while higher age at onset was generally associated with worse HRQoL trajectories. Accounting for these identified age-associated differences in disease progression could positively impact patient management and drug development efforts.

摘要

帕金森病(PD)通常被认为是一种与年龄相关的疾病,但患者的发病年龄可以相差几十年。衰老和与衰老相关的疾病可以独立于 PD 影响运动系统,并且先前已经提出,高龄与更严重的 PD 表型和加速进展相关。在这项工作中,我们研究了 PD 进展和衰老之间的相互作用如何影响与 PD 运动和非运动症状以及与健康相关的生活质量(HRQoL)和治疗特征相关的广泛结果。这项基于人群的队列研究基于来自瑞典南部的 1436 名 PD 患者,他们从入组开始进行了长达约 7.5 年的纵向随访(3470 次就诊涵盖 2285 个患者年,平均随访时间为 1.7 年)。发病年龄较高通常与运动症状的进展较快相关,但发病年龄较高的患者出现异动症和其他与左旋多巴相关的运动波动等运动症状的轨迹则不太严重,这是一个显著的例外。对于非运动症状的出现,观察到混合结果,而发病年龄较高通常与较差的 HRQoL 轨迹相关。考虑到这些与年龄相关的疾病进展差异,可以积极影响患者管理和药物开发工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cf9/8752787/712c8132cada/41598_2021_4356_Fig1_HTML.jpg

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