多巴胺 D2R 激动剂对健康男性心血管的影响:对临床的潜在影响

ISRN Neurology Pub Date : 2014-01-22 eCollection Date: 2014-01-01 DOI:10.1155/2014/956353
Khalid Abou Farha, Corine Baljé-Volkers, Wim Tamminga, Izaak den Daas, Sandra van Os
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引用次数: 0

摘要

多巴胺 D2 受体激动剂是有特发性帕金森病症状和体征的年轻患者的一线治疗选择。据报道,帕金森病患者使用 D2 受体激动剂与心力衰竭之间存在关联。为了最大限度地降低由此导致的心血管疾病发病率,需要找出其根本机制。在一项 I 期临床试验中,52 名健康男性受试者按照剂量递增方案服用了一种 D2 受体激动剂(普拉克索)。对静息血压、心率和衍生参数(包括脉压、脉动压力和心率压力乘积)的连续测量结果进行了分析。结果发现,大多数评估参数都有统计学意义和临床相关性的增加。有 10 名受试者因血压和/或心率显著升高而提前退出试验,原因是他们的血压和/或心率显著升高,需要立即使用静脉注射抢救药物(包括选择性 β -1 受体阻滞剂)进行干预。观察到的与药物相关的生命体征变化具有临床意义,可能解释了临床上报告的接受 D2 受体激动剂治疗的患者的部分心血管疾病发病率。我们建议,额外使用β-1阻断剂可能会降低长期服用D2受体激动剂的患者的心血管发病风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dopamine D2R Agonist-Induced Cardiovascular Effects in Healthy Male Subjects: Potential Implications in Clinical Settings.

Dopamine D2R Agonist-Induced Cardiovascular Effects in Healthy Male Subjects: Potential Implications in Clinical Settings.

Dopamine D2R Agonist-Induced Cardiovascular Effects in Healthy Male Subjects: Potential Implications in Clinical Settings.

Dopamine D2R Agonist-Induced Cardiovascular Effects in Healthy Male Subjects: Potential Implications in Clinical Settings.

Dopamine D2 receptor agonists represent a first line treatment option in young patients with signs and symptoms of idiopathic Parkinson's disease. An association between the use of D2 receptor agonists in Parkinson's disease patients and heart failure has been reported. The identification of the underlying mechanism is needed to minimize the resultant cardiovascular morbidity. In a phase I clinical trial, a D2 receptor agonist (pramipexole) was administered to 52 healthy male subjects following a dose escalation scheme. Serial measurements of resting blood pressure, heart rate, and derived parameters including pulse pressure, pulsatile stress, and rate pressure product were analysed. Statistically significant and clinically relevant increases in most of the assessed parameters were found. Ten subjects were removed prematurely from the trial because of clinically significant increases in blood pressure and/or heart rate requiring immediate intervention with IV rescue medications including a selective β -1 blocker. The observed drug-related changes in vital signs were of clinical relevance and might explain some of the cardiovascular morbidity reported in patients receiving D2 receptor agonist in clinical settings. We suggest that the additional use of a β -1 blocking agent might mitigate the risk of cardiovascular morbidity among patients receiving long-term D2 receptor agonists.

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