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载脂蛋白 E 促使帕金森病纵向冲动控制障碍进展。

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

机构信息

Taizhou Central Hospital (Taizhou University Hospital), No. 999, Donghai Avenue, economic development zone, Taizhou, 318000, Zhejiang, China.

出版信息

BMC Psychiatry. 2024 Sep 27;24(1):632. doi: 10.1186/s12888-024-06084-5.

Abstract

BACKGROUND

Impulse 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.

OBJECTIVE

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

METHODS

This 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.

RESULTS

44.3% (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.

CONCLUSIONS

This 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.

摘要

背景

冲动控制障碍(ICD)是帕金森病(PD)中越来越被认识到的并发症。ICD 的发病机制目前尚不清楚。该领域进行的遗传研究较少。

目的

我们旨在确定 APOE 与 ICD 之间的相关性,并确定 PD 中 ICD 的临床预测因子。

方法

这项研究纳入了来自帕金森进展标志物倡议的 287 名 PD 患者。他们接受了为期 5 年的随访,以调查 ICD 在 PD 中的进展情况。使用 Kaplan-Meier 和 Cox 回归分析评估 ICD 的累积发生率和潜在危险因素。

结果

在 5 年的随访期间,44.3%(31/70)携带 APOE ɛ4 的患者和 32.3%(70/217)不携带 APOE ɛ4 的患者发展为 ICD。在 PD 伴和不伴 ICD 发展组之间,基线时的年龄、MSEADLG 评分、ESS 评分、GDS 评分和 STAI 评分存在显著差异。在多变量 Cox 回归分析中,APOE ε4(HR=1.450,p=0.048)和 STAI 评分(HR=1.017,p=0.001)是 ICD 发展的预测因子。APOE ɛ4 组患者的基线 CSF Aβ42 和 CSF α-syn 水平明显低于无 APOE ɛ4 组患者。在 APOE ɛ4 组中,“低α-syn 水平”组和“低 ptau/tau 比值”组的 ICD 发生率显著更高。

结论

本研究为 APOE 基因在 PD 中 ICD 发展中的潜在作用提供了重要的见解。需要进一步的研究来证实我们的发现,并更详细地研究潜在的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a834/11438395/6682bf7abb40/12888_2024_6084_Fig1_HTML.jpg

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