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帕金森病认知衰退进展的预后评分。

Parkinson's disease prognostic scores for progression of cognitive decline.

机构信息

Research and Data Analysis Centre, GPO Box 1272, Aspley, QLD 4034, Australia.

University of Sunshine Coast, Thompson Institute, 12 Innovation Parkway, Birtinya, QLD, 4575, Australia.

出版信息

Sci Rep. 2019 Nov 25;9(1):17485. doi: 10.1038/s41598-019-54029-w.

Abstract

Clinical and biochemical diversity of Parkinson's disease (PD) presents a major challenge for accurate diagnosis and prediction of its progression. We propose, develop and optimize PD clinical scores as efficient integrated progression biomarkers for prediction of the likely rate of cognitive decline in PD patients. We considered 269 drug-naïve participants from the Parkinson's Progression Marker Initiative database, diagnosed with idiopathic PD and observed between 4 and 6 years. Nineteen baseline clinical and pathological measures were systematically considered. Relative variable importance and logistic regressions were used to optimize combinations of significant baseline measures as integrated biomarkers. Parkinson's disease cognitive decline scores were designed as new clinical biomarkers using optimally categorized baseline measures. Specificities and sensitivities of the biomarkers reached ~93% for prediction of severe rate of cognitive decline (with more than 5 points decline in 4 years on the Montreal Cognitive Assessment scale), and up to ~73% for mild-to-moderate decline (between 1 and 5 points decline). The developed biomarkers and clinical scores could resolve the long-standing clinical problem about reliable prediction of PD progression into cognitive deterioration. The outcomes also provide insights into the contributions of individual clinical and pathological measures to PD progression, and will assist with better-targeted treatment regiments, stratification of clinical trial and their evaluation.

摘要

帕金森病(PD)的临床和生化多样性对其准确诊断和进展预测提出了重大挑战。我们提出、开发和优化 PD 临床评分,作为预测 PD 患者认知下降速度的有效综合进展生物标志物。我们考虑了来自帕金森进展标志物倡议数据库的 269 名未经药物治疗的参与者,他们被诊断为特发性 PD,并在 4 到 6 年内进行了观察。系统地考虑了 19 项基线临床和病理测量。相对变量重要性和逻辑回归用于优化作为综合生物标志物的显著基线测量的组合。使用最优分类的基线测量值,设计了新的帕金森病认知衰退评分作为临床生物标志物。生物标志物的特异性和敏感性达到约 93%,用于预测严重的认知下降率(在蒙特利尔认知评估量表上 4 年内下降超过 5 分),轻度至中度下降率达到约 73%(下降 1 至 5 分)。所开发的生物标志物和临床评分可以解决长期存在的关于可靠预测 PD 进展为认知恶化的临床问题。结果还提供了对个体临床和病理测量对 PD 进展的贡献的深入了解,并将有助于更好地靶向治疗方案、临床试验的分层及其评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2033/6877592/79cb18dce597/41598_2019_54029_Fig1_HTML.jpg

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