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帕金森病预后模型的系统评价

Systematic review of prognostic models in Parkinson's disease.

作者信息

Li Yan, McDonald-Webb Millie, McLernon David J, Counsell Carl E, Macleod Angus D

机构信息

Institute of Applied Health Sciences, University of Aberdeen, Polwarth Building, Foresterhill, Aberdeen, UK.

School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Polwarth Building, Foresterhill, Aberdeen, UK.

出版信息

NPJ Parkinsons Dis. 2025 Aug 29;11(1):266. doi: 10.1038/s41531-025-01112-x.

DOI:10.1038/s41531-025-01112-x
PMID:40883335
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12397436/
Abstract

Predicting outcomes for people with Parkinson's (PwP) can enable better information provision, personalised treatments, and enhanced trial design. It is unclear what prognostic models are optimal for use. We systematically reviewed previously published prognostic models for PwP, assessed quality, and made recommendations. We searched MEDLINE and EMBASE for studies developing/validating models predicting clinical outcomes in PwP. We assessed risk of bias and applicability using the PROBAST tool. We screened 1024 references and identified 25 studies (41 prognostic models). The most common outcomes were falls (11 studies), dementia (7) and motor complications (4). Most models made short-term predictions (60% ≤2 years). All studies had concerns about bias, e.g., inadequate population details (n = 16), suboptimal methods for missing data (n = 21), and no external validation (n = 22). 13 models had sufficient information to be used in practice. Further development and validation of prognostic models is needed which follows existing guidelines to reduce risk of bias.

摘要

预测帕金森病患者(PwP)的预后可以提供更好的信息、个性化治疗并优化试验设计。目前尚不清楚哪种预后模型是最适合使用的。我们系统回顾了先前发表的针对PwP的预后模型,评估了其质量并给出了建议。我们在MEDLINE和EMBASE中检索了开发/验证预测PwP临床结局模型的研究。我们使用PROBAST工具评估偏倚风险和适用性。我们筛选了1024篇参考文献,确定了25项研究(41种预后模型)。最常见的结局是跌倒(11项研究)、痴呆(7项)和运动并发症(4项)。大多数模型进行短期预测(60%≤2年)。所有研究都存在偏倚问题,例如,人群细节不足(n = 16)、处理缺失数据的方法欠佳(n = 21)以及缺乏外部验证(n = 22)。13种模型有足够的信息可用于实际应用。需要按照现有指南进一步开发和验证预后模型,以降低偏倚风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6813/12397436/31aa18f17d60/41531_2025_1112_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6813/12397436/31aa18f17d60/41531_2025_1112_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6813/12397436/31aa18f17d60/41531_2025_1112_Fig2_HTML.jpg

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本文引用的文献

1
Assessing Performance and Clinical Usefulness in Prediction Models With Survival Outcomes: Practical Guidance for Cox Proportional Hazards Models.评估生存结局预测模型的性能和临床实用性:Cox 比例风险模型的实用指南。
Ann Intern Med. 2023 Jan;176(1):105-114. doi: 10.7326/M22-0844. Epub 2022 Dec 27.
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Validation of prediction models in the presence of competing risks: a guide through modern methods.存在竞争风险时预测模型的验证:现代方法指南
BMJ. 2022 May 24;377:e069249. doi: 10.1136/bmj-2021-069249.
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External validation of prognostic models: what, why, how, when and where?
预后模型的外部验证:是什么、为什么、如何、何时以及何地?
Clin Kidney J. 2020 Nov 24;14(1):49-58. doi: 10.1093/ckj/sfaa188. eCollection 2021 Jan.
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Multivariate prediction of dementia in Parkinson's disease.帕金森病痴呆的多变量预测
NPJ Parkinsons Dis. 2020 Aug 25;6:20. doi: 10.1038/s41531-020-00121-2. eCollection 2020.
5
Regression with a right-censored predictor using inverse probability weighting methods.使用逆概率加权法对右删失预测变量进行回归分析。
Stat Med. 2020 Nov 30;39(27):4001-4015. doi: 10.1002/sim.8704. Epub 2020 Aug 10.
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Calculating the sample size required for developing a clinical prediction model.计算开发临床预测模型所需的样本量。
BMJ. 2020 Mar 18;368:m441. doi: 10.1136/bmj.m441.
7
Personalized prediction of depression in patients with newly diagnosed Parkinson's disease: A prospective cohort study.对新发帕金森病患者抑郁的个体化预测:一项前瞻性队列研究。
J Affect Disord. 2020 May 1;268:118-126. doi: 10.1016/j.jad.2020.02.046. Epub 2020 Feb 28.
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BMC Med. 2019 Dec 16;17(1):230. doi: 10.1186/s12916-019-1466-7.
9
Predicting motor, cognitive & functional impairment in Parkinson's.预测帕金森病患者的运动、认知和功能障碍。
Ann Clin Transl Neurol. 2019 Aug;6(8):1498-1509. doi: 10.1002/acn3.50853. Epub 2019 Jul 26.
10
Predictors of motor complications in early Parkinson's disease: A prospective cohort study.早期帕金森病运动并发症的预测因素:一项前瞻性队列研究。
Mov Disord. 2019 Aug;34(8):1174-1183. doi: 10.1002/mds.27783. Epub 2019 Jul 8.