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药物性帕金森病:特发性帕金森病的强烈预测因子。

Drug-induced Parkinsonism: A strong predictor of idiopathic Parkinson's disease.

机构信息

Marcus Institute for Aging Research at Hebrew SeniorLife, Boston, Massachusetts, United States of America.

Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts, United States of America.

出版信息

PLoS One. 2021 Mar 1;16(3):e0247354. doi: 10.1371/journal.pone.0247354. eCollection 2021.

Abstract

BACKGROUND

Although Idiopathic Parkinson's disease (IPD) develops in considerable patients with drug-induced Parkinsonism (DIP), the association hasn't been well defined. We aimed to evaluate the underlying association and risk factors of DIP and IPD.

METHODS

A retrospective cohort study using National Health Insurance Claims data in 2011-2016 was conducted. New-onset DIP patients in 2012 were selected and matched with active controls having diabetes mellitus at a 1:4 ratio by age, sex, and Charlson's Comorbidity Index score. Comorbidity, causative drugs, and prescription days were evaluated as covariates.

RESULTS

A total of 441 DIP were selected. During the 4-year follow up, 14 IPD events in the DM group but 62 events in the DIP group were observed (adjusted hazard ratio, HR: 18.88, 95% CI, 9.09-39.22, adjusting for comorbidities and causative drugs). IPD diagnosis in DIP was observed high in males compared to females (15.58/13.24%). The event was the most within the 1st year follow-up, mean days 453 (SD 413.36). Subgroup analysis in DIP showed calcium channel blocker (verapamil, diltiazem, and flunarizine) was significantly associated with increased IPD risk (HR: 2.24, 95% CI, 1.27-3.93).

CONCLUSION

Increased IPD in DIP patients might not be from the causal toxicity of antidopaminergic effects but from a trigger by the causative drugs on the DIP patients who already had subclinical IPD pathology. DIP can serve as a strong proxy for IPD incidence. Subjects who develop DIP should be monitored carefully for potential IPD incidence.

摘要

背景

虽然特发性帕金森病(IPD)在相当数量的药物诱导帕金森病(DIP)患者中发展,但两者之间的关联尚未得到很好的定义。我们旨在评估 DIP 和 IPD 的潜在关联和危险因素。

方法

使用 2011-2016 年国家健康保险索赔数据进行回顾性队列研究。选择 2012 年新发的 DIP 患者,并按年龄、性别和 Charlson 合并症指数评分与糖尿病患者以 1:4 的比例进行匹配。将共病、致病药物和处方天数作为协变量进行评估。

结果

共选择了 441 例 DIP。在 4 年的随访期间,DM 组观察到 14 例 IPD 事件,而 DIP 组观察到 62 例事件(调整后的危险比,HR:18.88,95%CI:9.09-39.22,调整了共病和致病药物)。与女性相比,DIP 中的 IPD 诊断在男性中更为常见(15.58/13.24%)。事件发生在随访的第 1 年内最高,平均天数为 453(SD 413.36)。DIP 的亚组分析显示,钙通道阻滞剂(维拉帕米、地尔硫卓和氟桂嗪)与 IPD 风险增加显著相关(HR:2.24,95%CI:1.27-3.93)。

结论

DIP 患者中 IPD 的增加可能不是由于抗多巴胺能作用的因果毒性引起的,而是由于致病药物对已经患有亚临床 IPD 病理的 DIP 患者产生了触发作用。DIP 可以作为 IPD 发病率的一个强有力的替代指标。出现 DIP 的患者应密切监测潜在的 IPD 发病率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbf5/7920346/e8f348d0b82e/pone.0247354.g001.jpg

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