Why the study?
Does the use of dopamine agonists (pramipexole or cabergoline) increase the risk of heart failure in Parkinson's disease patients?
Does the use of dopamine agonists (pramipexole or cabergoline) increase the risk of heart failure in Parkinson's disease patients?
This review highlights a potential safety signal of increased heart failure risk associated with the dopamine agonists pramipexole and cabergoline in patients with Parkinson's disease.
INTRODUCTION: Dopamine agonists (DAs) are frequently used to treat early or advanced Parkinson's disease (PD) patients. They have been shown to be efficacious for the treatment of motor symptoms and for delaying levodopa-induced dyskinesias. However, their utilization is limited by the risk of adverse drug reactions, some of which affect the cardiovascular system. Recently, the US FDA identified a possible association between exposure to pramipexole and the risk of heart failure. AREAS COVERED: This article begins by reviewing the pharmacodynamic and cardiovascular effects of DAs on PD patients. Pharmacoepidemiological studies about the association between DAs and heart failure are then evaluated. EXPERT OPINION: Four nested case-control studies were reviewed. In general, results showed higher heart failure risk following use of pramipexole or cabergoline. Although the effects of cabergoline may be explained by the induction of cardiac valve fibrosis, the basis for the significantly increased risk associated with pramipexole is unclear. It remains to be determined if these are dose-related effects, at what point they occur during the course of treatment, and if the risk is the same for all patients irrespective of other potential modifying factors, such as age and sex.
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Perez‐Lloret et al. (2014) studied this question.
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