Evidence map›Paper›PMID 39334114›Full record

ArticleBMC psychiatry2024

APOE contributes to longitudinal impulse control disorders progression in Parkinson's disease.

Linxi Chen, Xinwei He, Lingqun Mao, Peng Liu

Abstract read
In one paragraph

Article in BMC psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Linxi ChenTaizhou Central Hospital (Taizhou University Hospital), No. 999, Donghai Avenue, economic development zone, Taizhou, 318000, Zhejiang, China.
Xinwei HeTaizhou Central Hospital (Taizhou University Hospital), No. 999, Donghai Avenue, economic development zone, Taizhou, 318000, Zhejiang, China.
Lingqun MaoTaizhou Central Hospital (Taizhou University Hospital), No. 999, Donghai Avenue, economic development zone, Taizhou, 318000, Zhejiang, China.
Peng LiuTaizhou Central Hospital (Taizhou University Hospital), No. 999, Donghai Avenue, economic development zone, Taizhou, 318000, Zhejiang, China. liupeng@tzc.edu.cn.

Funding

Taizhou University Medical Special Research Project G2023FSXY05the Medical and Health Science and Technology Project of Zhejiang Province 2024KY539the Zhejiang Provincial Natural Science Foundation of China grant number LQ24H090009
6 · The paper itself

Abstract

backgroundImpulse control disorders (ICDs) are an increasingly recognized complication in Parkinson disease (PD). The pathogenesis of ICDs is currently unclear. Few genetic studies have been conducted in this area.

objectiveWe aimed to ascertain the correlation between APOE and ICDs, and identify clinical predictors of ICDs in PD.

methodsThis study included 287 PD patients from the Parkinson's Progression Markers Initiative. They were followed up to investigate the progression of ICDs over a period of 5 years. The cumulative incidence of ICDs and potential risk factors were evaluated using Kaplan-Meier and Cox regression analyses.

results44.3% (31/70) patients with APOE ɛ4 and 32.3% (70/217) patients without APOE ɛ4 developed ICDs during the five-year follow up period. There were significant differences between the PD with and without ICDs development group in age, MSEADLG score, ESS score, GDS score, and STAI score at baseline. In multivariable Cox regression analysis, APOE ε4 (HR = 1.450, p = 0.048) and STAI score (HR = 1.017, p = 0.001) were predictors of the development of ICDs. Patients with APOE ɛ4 group showed significantly lower CSF Aβ42 and CSF α-syn level than patients without APOE ɛ4 group at baseline. In patients with APOE ɛ4 group, the "low α-syn level" group and the "low ptau/tau ratio" group had a significantly higher incidence of ICDs, respectively.

conclusionsThis study provides important insights into the potential role of the APOE gene in the development of ICDs in PD. Further studies are needed to confirm our findings and to investigate the underlying mechanisms in more detail.

Indexed as

Disease ProgressionDisruptive, Impulse Control, and Conduct DisordersParkinson DiseaseAgedAmyloid beta-PeptidesApolipoprotein E4Apolipoproteins EFemaleHumansIncidenceLongitudinal StudiesMaleMiddle AgedRisk Factorstau ProteinsAmyloid beta-PeptidesApolipoprotein E4Apolipoproteins Etau ProteinsAPOECox regressionImpulse control disordersParkinson’s diseaseΑ-synuclein

Identifiers

PMID39334114
PMCPMC11438395

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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.