Evidence map›Paper›PMID 41644752›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2026

Predictive factors of global cognitive impairment in de novo Parkinson disease with normal cognition at baseline: a 10-year cohort study.

Xin Wang, Lu Tian

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Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

2 authors.

Xin WangDepartment of Neurosurgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China. nswangxin@163.com.ORCID http://orcid.org/0000-0002-9982-4397
Lu TianEconomic Operation Management Office, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, Shandong, China.

Funding

Natural Science Foundation of Shandong Province ZR2022QH368
6 · The paper itself

Abstract

objectiveCognitive impairment (CI) constitutes a heavy burden to patients with Parkinson disease (PD) and their care partners. This study was to investigate the predictors of cognitive decline in de novo PD patients during the 10-year follow-up period.

methodsPD patients from the Parkinson’s Progression Marker Initiative (PPMI) database with normal baseline global cognition measured by Montreal Cognitive Assessment (MoCA) were included and stratified by their 10-year global cognitive performance. A total of 59 baseline clinical, biological, and radiological variables were compared separately between the patient groups with and without CI (combing mild cognitive impairment and dementia). A predictive model was constructed, followed by the evaluation of model performance using the areas under the receiver operating characteristic curve (AUC).

resultsA total of 155 subjects with normal global cognition at baseline were included, in which 31 patients developed CI during the 10-year follow-up period. After feature selection, a total of 6 features including age were significantly associated with the development of CI. These features were included into the final predictive model. The predictive accuracy of our model was obviously higher than the model using age alone (AUC, 0.868 [95%, 0.800-0.936] vs. 0.734 [0.646–0.822], p ˂ 0.01).

conclusionsUsing our model, risks of CI during the 10-year follow-up period could be predicted with high accuracy. Our study indicated the possibilities and necessities of earlier identification of individuals with higher risks of cognitive decline in the long-term. Further studies are needed before the established application of our model into clinical practice.

Indexed as

Cognitive DysfunctionParkinson DiseaseAgedCohort StudiesDisease ProgressionFemaleFollow-Up StudiesHumansMaleMental Status and Dementia TestsMiddle AgedNeuropsychological TestsGlobal cognitive impairmentLong-term follow-up periodMontreal cognitive assessmentParkinson diseasePredictive model

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.