Literature DB >> 22288503

No clinically significant valvular regurgitation in long-term cabergoline treatment for prolactinoma.

Irene Halperin1, Javier Aller, César Varela, Mireia Mora, Ainhoa Abad, Ada Doltra, Alicia Estrella Santos, Esther Batista, Pablo García-Pavía, Marta Sitges, Jesús G Mirelis, Tomás Lucas, Manel Puig-Domingo.   

Abstract

BACKGROUND: An association between treatment for Parkinson's disease with certain dopaminergic drugs and development of cardiac valve impairment has been reported. Recent studies in hyperprolactinaemic patients treated with cabergoline (CAB) have shown either no significant findings or mild tricuspid regurgitation. <br> OBJECTIVE: To determine the prevalence of cardiac valve dysfunction in patients with hyperprolactinaemic conditions chronically treated with CAB or bromocriptine (BR). <br> DESIGN: Retrospective, multicentric, cross-sectional study of cases vs controls. PATIENTS: Eighty-three hyperprolactinaemic patients (15 men, 68 women aged 16·7-63 years; 64% microprolactinomas, 28% macroprolactinomas and 8% other etiologies) from three Spanish university hospitals chronically treated with BR (14-562·5 weeks, cumulative dose 5603 ± 7729 mg) or CAB (12-765 weeks, 217·4 ± 306·6 mg). MEASUREMENTS: Transthoracic echocardiographic assessment of valvular regurgitation and thickening, mitral valve tenting area and left-ventricular ejection fraction from 83 patients were compared with results from 58 age- and sex-matched controls and correlated with cumulative doses of dopaminergic drugs. <br> RESULTS: No significant differences in valvular regurgitation, valve thickness or any other echocardiographic parameter were observed between controls and patients, except for 15 patients in the higher quartile of CAB cumulative dose (>180 mg), with increased prevalence of mild tricuspid regurgitation (6/15, 40% vs 8/58, 13·8%, P = 0·024; OR 4·1; 1·1-14·9). High BR cumulative dose was associated with no significant findings. <br> CONCLUSIONS: No increased valvular involvement was found after long-term dopaminergic therapy for hyperprolactinaemia except for a significant increase in mild tricuspid regurgitation associated with high cumulative doses of CAB; BR seems spared from this adverse effect, although the low number of cases limits this analysis. Cumulative dose registry and long-term studies are warranted to definitely clarify this item.
© 2012 Blackwell Publishing Ltd.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22288503     DOI: 10.1111/j.1365-2265.2012.04349.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  5 in total

Review 1.  Screening for valve disease in patients with hyperprolactinaemia disorders prescribed cabergoline: a service evaluation and literature review.

Authors:  David Gamble; Rachel Fairley; Roderick Harvey; Colin Farman; Nathan Cantley; Stephen J Leslie
Journal:  Ther Adv Drug Saf       Date:  2017-04-25

2.  Incidence of Cabergoline-Associated Valvulopathy in Primary Care Patients With Prolactinoma Using Hard Cardiac Endpoints.

Authors:  Craig Edward Stiles; Guy Lloyd; Sanjeev Bhattacharyya; Richard Paul Steeds; Kambiz Boomla; Jonathan Paul Bestwick; William Martyn Drake
Journal:  J Clin Endocrinol Metab       Date:  2021-01-23       Impact factor: 5.958

3.  Treatment results of high dose cabergoline as an adjuvant therapy in six patients with established severe ovarian hyper stimulation syndrome.

Authors:  Nasrin Saharkhiz; Azadeh Akbari Sene; Saghar Salehpour; Maryam Tamimi; Masoumeh Vasheghani Farahani; Kourosh Sheibani
Journal:  Iran J Reprod Med       Date:  2014-10

4.  Long-term cardiac (valvulopathy) safety of cabergoline in prolactinoma.

Authors:  Shruti Khare; Anurag R Lila; Rishikesh Patil; Milind Phadke; Prafulla Kerkar; Tushar Bandgar; Nalini S Shah
Journal:  Indian J Endocrinol Metab       Date:  2017 Jan-Feb

5.  Incidence of heart valve disease in women treated with the ergot-derived dopamine agonist bromocriptine.

Authors:  Marianne F Clausen; Rasmus Rørth; Christian Torp-Pedersen; Lucas Malta Westergaard; Peter E Weeke; Gunnar Gislason; Lars Køber; Emil Fosbøl; Søren Lund Kristensen
Journal:  BMC Cardiovasc Disord       Date:  2021-12-28       Impact factor: 2.298

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.