Crispo James A G, Willis Allison W, Thibault Dylan P, Fortin Yannick, Emons Matthew, Bjerre Lise M, Kohen Dafna E, Perez-Lloret Santiago, Mattison Donald, Krewski Daniel
McLaughlin Center for Population Health Risk Assessment University of Ottawa Ottawa Ontario Canada.
Fulbright Canada Student University of Pennsylvania Philadelphia Pennsylvania USA.
Mov Disord Clin Pract. 2015 Dec 24;3(3):257-267. doi: 10.1002/mdc3.12286. eCollection 2016 May-Jun.
Knowledge of possible cardiovascular risks from Parkinson's disease (PD) medications is critical to informing safe and effective treatment decisions. The objective of our study was to determine whether PD patients treated with nonergot dopamine agonists (DAs) are at increased risk of adverse cardiovascular or cerebrovascular outcomes, relative to PD patients receiving other treatments.
Matched case-control studies were conducted within a cohort of 14,122 inpatients receiving treatment for PD who were identified in the Cerner Health Facts database. Primary outcomes were associations between nonergot DA use and diagnosis of adverse cardiovascular events (acute myocardial infarction, heart failure [HF], hypotension, and valvulopathy). Secondary outcomes included associations between nonergot DA use and diagnosis of adverse cerebrovascular events (cerebrovascular accident and ischemic stroke) and odds of significant exposure-outcome relationships by patient factors.
HF was the only adverse event that demonstrated a significant association with nonergot DA use. Individuals treated with pramipexole were more likely to be diagnosed with HF, relative to no use (adjusted odds ratio [AOR]: 1.28; 95% confidence interval [CI]: 1.07-1.53). The association between pramipexole and HF was greater among individuals treated with pramipexole monotherapy (relative to levodopa monotherapy) (AOR, 1.50; 95% CI: 1.09-2.06). Compared to nonusers, men and older individuals treated with pramipexole were more likely to be diagnosed with HF.
Results from our study suggest an association between pramipexole use and HF. Findings warrant replication; however, individuals with PD and independent risk factors for, or a history of, HF may benefit from limited use of this drug.
了解帕金森病(PD)药物可能存在的心血管风险对于做出安全有效的治疗决策至关重要。我们研究的目的是确定与接受其他治疗的PD患者相比,接受非麦角多巴胺激动剂(DAs)治疗的PD患者发生不良心血管或脑血管事件的风险是否增加。
在Cerner健康事实数据库中识别出的14122名接受PD治疗的住院患者队列中进行了匹配病例对照研究。主要结局是非麦角DA使用与不良心血管事件(急性心肌梗死、心力衰竭[HF]、低血压和瓣膜病)诊断之间的关联。次要结局包括非麦角DA使用与不良脑血管事件(脑血管意外和缺血性中风)诊断之间的关联以及按患者因素划分的显著暴露-结局关系的比值比。
HF是唯一与非麦角DA使用有显著关联的不良事件。与未使用相比,接受普拉克索治疗的个体更有可能被诊断为HF(调整后的比值比[AOR]:1.28;95%置信区间[CI]:1.07-1.53)。在接受普拉克索单药治疗的个体中(相对于左旋多巴单药治疗),普拉克索与HF之间的关联更大(AOR,1.50;95%CI:1.09-2.06)。与未使用者相比,接受普拉克索治疗的男性和老年个体更有可能被诊断为HF。
我们的研究结果表明普拉克索使用与HF之间存在关联。研究结果有待重复验证;然而,患有PD且有HF独立危险因素或HF病史的个体可能会从有限使用这种药物中获益。