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Bromocriptine use and the risk of valvular heart disease
Louis C S Tan1, Kenneth K C Ng, Wing-Lok Au
1Parkinson's Disease and Movement Disorders Centre, National Neuroscience Institute, Singapore. louis_tan@nni.com.sg
Insights
Parkinson's disease patients taking bromocriptine, a dopamine agonist, face an increased risk of valvular heart disease. This risk is dose-dependent, similar to pergolide, highlighting potential cardiovascular concerns with these medications.
Area of Science:
- Neurology
- Cardiology
- Pharmacology
Background:
- Pergolide and cabergoline are known to increase valvular heart disease (VHD) risk in Parkinson's disease (PD) patients.
- Bromocriptine, another dopamine agonist (DA) derived from ergot, has partial 5-HT(2B) activity, raising questions about its VHD risk.
- The association between bromocriptine and VHD remains uncertain.
Purpose of the Study:
- To assess the frequency of VHD in PD patients treated with bromocriptine.
- To compare the VHD risk in bromocriptine users versus pergolide users and a control group of PD patients not on DAs.
- To investigate the relationship between cumulative bromocriptine dose and VHD development.
Main Methods:
- A comparative study involving 72 PD patients on bromocriptine, 21 on pergolide, and 47 controls.
- Transthoracic echocardiography was performed on all participants.
- Echocardiographic studies were independently reviewed by a blinded cardiologist.
Main Results:
- Bromocriptine users showed a 3.32-fold increased risk of abnormal valvular regurgitation compared to controls (adjusted OR, 1.11-9.92; P=0.03).
- Pergolide users had a 3.66-fold increased risk (adjusted OR, 1.22-10.97; P=0.02).
- Higher cumulative bromocriptine doses correlated significantly with increased risk of mild and moderate-severe regurgitations (P for trend, 0.005 and 0.019).
Conclusions:
- Bromocriptine use is associated with an elevated risk of developing valvular heart disease in Parkinson's disease patients.
- The risk of VHD associated with bromocriptine is cumulative and dose-dependent.
- These findings suggest careful monitoring for VHD in PD patients using bromocriptine, particularly with long-term or high-dose therapy.
Abstract:
It has been reported that patients on pergolide and carbergoline have an increased risk of developing valvular heart disease. It is uncertain if bromocriptine, an ergot-derived dopamine agonist (DA) with partial 5-HT(2B) activity, is associated with a similar risk. We assessed the frequency of valvular heart disease in Parkinson's disease (PD) patients on bromocriptine compared to pergolide and a control group of PD patients who had not been treated on any DA. Seventy-two PD patients on bromocriptine, 21 patients on pergolide, and 47 control PD patients were recruited. Transthoracic echocardiographic studies were performed and reviewed by a blinded cardiologist. The risk for the bromocriptine group to develop any abnormal valvular regurgitation was 3.32 (adjusted OR, 95% CI: 1.11-9.92, P = 0.03) compared to controls, whereas the risk for the pergolide group was 3.66 (adjusted OR, 95% CI: 1.22-10.97, P = 0.02). When cumulative dose of bromocriptine was analyzed by quartiles, patients with a greater exposure to bromocriptine had significantly higher risk of developing both mild and moderate-severe regurgitations (P for trend, 0.005 and 0.019, respectively). This study demonstrated that bromocriptine use was associated with an increased risk of developing valvular heart disease, which occurred in a cumulative dose-dependent manner.
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