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既往抗精神病药物暴露与老年队列帕金森病风险。

Past exposure to neuroleptic drugs and risk of Parkinson disease in an elderly cohort.

机构信息

INSERM Unit 897, Bordeaux, France.

出版信息

Neurology. 2012 Oct 9;79(15):1615-21. doi: 10.1212/WNL.0b013e31826e25ce. Epub 2012 Sep 26.

Abstract

OBJECTIVE

Neuroleptics and neuroleptic-like drugs are known to induce parkinsonism, which may reveal underlying Parkinson disease (PD) in some cases. We assessed the long-term risk of developing PD after past exposure to these drugs, in a 15-year prospective population-based elderly cohort study.

METHODS

We used the Cox proportional hazards model to assess the relation between past exposure to neuroleptics and the risk of developing incident PD. All incident cases of parkinsonism were identified by standardized procedure and validated by a committee of experts.

RESULTS

Of 2,991 subjects followed, 117 developed parkinsonism and 43 developed probable PD during follow-up, of whom 22.2% and 32.6%, respectively, had been exposed to neuroleptics, compared to 16.6% for subjects without parkinsonism. About a third of subjects presented transient parkinsonism during drug exposure. After adjustment for gender and past occupation, past exposure to neuroleptics was associated with incident PD (relative risk, 3.16; 95% confidence interval [CI], 1.65-6.04). The relative risk was 3.65 (95% CI, 1.41-9.45) for benzamides and 2.59 (95% CI, 1.23-5.43) for phenothiazines. The population-attributable fraction of the risk for developing PD was 8.2% for benzamides and 12.2% for phenothiazines.

CONCLUSIONS

In a French elderly cohort, the risk of probable PD was increased by 3.2-fold after exposure to neuroleptics. This finding suggests the necessity of limiting the use of such drugs in elderly people.

摘要

目的

神经安定药和类神经安定药已知可引起帕金森病,在某些情况下,这可能揭示了潜在的帕金森病(PD)。我们在一项为期 15 年的前瞻性基于人群的老年队列研究中,评估了过去接触这些药物后发生 PD 的长期风险。

方法

我们使用 Cox 比例风险模型评估过去接触神经安定药与发生 PD 的风险之间的关系。所有帕金森病的新发病例均通过标准化程序进行评估,并由专家委员会进行验证。

结果

在 2991 名随访的受试者中,117 名出现帕金森病,43 名出现可能的 PD,其中分别有 22.2%和 32.6%在随访期间曾接触过神经安定药,而无帕金森病的受试者分别为 16.6%。约三分之一的受试者在药物暴露期间出现短暂性帕金森病。在调整性别和过去职业后,过去接触神经安定药与新发 PD 相关(相对风险,3.16;95%置信区间[CI],1.65-6.04)。苯甲酰胺的相对风险为 3.65(95% CI,1.41-9.45),而苯并噻嗪的相对风险为 2.59(95% CI,1.23-5.43)。苯甲酰胺和苯并噻嗪发生 PD 的人群归因分数分别为 8.2%和 12.2%。

结论

在法国老年队列中,接触神经安定药后 PD 的风险增加了 3.2 倍。这一发现表明有必要限制此类药物在老年人中的使用。

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