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抗胆碱能负担及临床人口统计学特征对帕金森病患者新发痴呆的影响

Impact of Anticholinergic Burden and Clinical-Demographic Characteristics on Incident Dementia in Parkinson Disease.

作者信息

Pham Nguyen Thanh Phuong, Thibault Dylan, Gray Shelly L, Weintraub Daniel, Willis Allison W

机构信息

Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.

Department of Neurology Translational Center for Excellence for Neuroepidemiology and Neurological Outcomes Research, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.

出版信息

J Geriatr Psychiatry Neurol. 2025 Jan 7;38(4):8919887241313376. doi: 10.1177/08919887241313376.

Abstract

PURPOSE

Anticholinergic medication use measured via the Anticholinergic Cognitive Burden (ACB) scale has been associated with an increased dementia incidence in older adults but has not been explored specifically for Parkinson disease dementia (PDD). We used adjusted Cox models to estimate the risk of incident PDD associated with demographic factors, clinical characteristics, and time-varying total ACB in a longitudinal, deeply-phenotyped prospective PD cohort.

MAJOR FINDINGS

56.5% of study participants were taking ACB-scale drugs at enrollment. Increasing age, motor symptom burden and psychosis were associated with PDD risk. Female sex and educational achievement were protective against PDD. ACB categories were not associated with PDD overall, but depression and impulse control disorder were strongly associated with PDD in a subsample with high baseline ACB.

CONCLUSIONS

Patient and clinical factors modify PDD risk. PD drug safety and drug-disease interaction studies may require considering multiple mechanisms and including dose-based, prospectively acquired medication exposure measures.

摘要

目的

通过抗胆碱能认知负担(ACB)量表衡量的抗胆碱能药物使用与老年人痴呆发病率增加有关,但尚未针对帕金森病痴呆(PDD)进行专门研究。我们使用校正后的Cox模型,在一个纵向、深度表型的前瞻性帕金森病队列中,估计与人口统计学因素、临床特征和随时间变化的总ACB相关的PDD发病风险。

主要发现

56.5%的研究参与者在入组时正在服用ACB量表药物。年龄增长、运动症状负担和精神病与PDD风险相关。女性和教育程度对PDD有保护作用。ACB类别总体上与PDD无关,但在基线ACB较高的子样本中,抑郁和冲动控制障碍与PDD密切相关。

结论

患者和临床因素会改变PDD风险。帕金森病药物安全性和药物-疾病相互作用研究可能需要考虑多种机制,并纳入基于剂量的、前瞻性获得的药物暴露测量。

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