ergoline and Endocrine-System-Diseases

The cardiac valvular risk associated with lower exposure to cabergoline in common endocrine conditions such as hyperprolactinemia is unknown.. We performed a cross-sectional, case-control echocardiographic study to assess the valvular status in 102 subjects receiving cabergoline for endocrine disorders and 51 matched control subjects. Cabergoline treatment ranged from 12 to 228 months, with a cumulative dose of 18-1718 mg. Valvular regurgitation was equally prevalent in both groups and was almost exclusively mild. Two cabergoline-treated subjects had moderate mitral regurgitation; there was no relationship between cabergoline dose and the presence or severity of mitral valve regurgitation (P=NS). Mitral valve tenting area was significantly greater in the cabergoline group when compared with the control subjects (P=0.03). Mitral valve leaflet thickening was observed in 5.9% of cabergoline-treated subjects; no relationship with the cumulative cabergoline dose was found. No patient had aortic or tricuspid valvular restriction.. No significantly increased risk of clinically relevant cardiac valve disorders was found in subjects treated with long-term cabergoline therapy at the doses used in endocrine practice. While exposure to cabergoline appears to be safe during low-dose long-term therapy, an association with subclinical changes in mitral valve geometry cannot be completely excluded.

Topics: Adult; Aged; Cabergoline; Cross-Sectional Studies; Dopamine Agonists; Echocardiography; Endocrine System Diseases; Ergolines; Female; Heart Valve Diseases; Humans; Male; Middle Aged; Mitral Valve; Mitral Valve Insufficiency; Risk Factors

Topics: Bromocriptine; Costs and Cost Analysis; Endocrine System Diseases; Ergolines; Female; Humans; United Kingdom

Topics: Bromocriptine; Dopamine; Endocrine System Diseases; Ergolines; Humans; Prolactin; Prolactin Release-Inhibiting Factors; Receptors, Drug; Synaptic Transmission