Literature DB >> 9024247

Effect of different dopaminergic agents in the treatment of acromegaly.

A Colao1, D Ferone, P Marzullo, A Di Sarno, G Cerbone, F Sarnacchiaro, S Cirillo, B Merola, G Lombardi.   

Abstract

Medical treatment of acromegaly with dopamine agonists possesses 2 main advantages: the oral administration and the low costs. In this study, we reported on the results of chronic treatments with quinagolide (CV 205-502), cabergoline (CAB) and long-acting depot preparation of bromocriptine (BRC-LAR) in 34 acromegalics. Patients were divided into three groups on the basis of different treatment: CV 205-502 given to 16 patients at the dose of 0.3-0.6 mg/day for 6 months; CAB given to 11 patients at the dose of 1.0-2.0 mg weekly for 6 months; and BRC-LAR injected into 7 patients at the dose of 100 mg/month for 6-12 months. Basal and oral glucose tolerance test-stimulated serum GH levels, basal and TRH-stimulated PRL levels, plasma insulin-like growth factor I (IGF-I) levels, computed tomography scan, and/or magnetic resonance imaging were assessed before and quarterly during treatments. The chronic administration of CV 205-502, CAB, and BRC-LAR caused a significant decrease of circulating GH, IGF-I, and PRL levels (P < 0.005). Normalization of circulating GH and IGF-I levels was obtained in 7 of 16 (43.8%) patients treated with CV 205-502. Serum GH response to oral glucose tolerance test (oGTT) significantly improved (P < 0.005), and PRL levels were significantly suppressed during treatments. No correlation was found between basal and TRH-stimulated PRL levels and GH suppression during different therapies. Immunohistochemical staining revealed 19 GH-positive and 10 GH + PRL-positive adenomas. A significant association was found between GH/PRL staining and responsiveness to chronic treatments (chi 2 = 7.985, P < 0.005). Three patients had significant adenoma shrinkage. Slight nausea and hypotension which spontaneously disappeared within therapy progression, were referred by 5/16 patients during CV 205-502 and 2/7 during BRC-LAR. The results of this study indicate that CAB and BRC-LAR cannot be considered as useful medical approaches for acromegalics, whereas CV 205-502 normalized circulating GH and IGF-I levels in 47.8% of patients.

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Year:  1997        PMID: 9024247     DOI: 10.1210/jcem.82.2.3648

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  32 in total

Review 1.  Italian Society for the Study of Diabetes (SID)/Italian Endocrinological Society (SIE) guidelines on the treatment of hyperglycemia in Cushing's syndrome and acromegaly.

Authors:  M G Baroni; F Giorgino; V Pezzino; C Scaroni; A Avogaro
Journal:  J Endocrinol Invest       Date:  2015-12-30       Impact factor: 4.256

2.  First-line therapy of acromegaly: a statement of the A.L.I.C.E. (Acromegaly primary medical treatment Learning and Improvement with Continuous Medical Education) Study Group.

Authors:  A Colao; E Martino; P Cappabianca; R Cozzi; M Scanarini; E Ghigo
Journal:  J Endocrinol Invest       Date:  2006-12       Impact factor: 4.256

Review 3.  Acromegaly.

Authors:  Anat Ben-Shlomo; Shlomo Melmed
Journal:  Endocrinol Metab Clin North Am       Date:  2008-03       Impact factor: 4.741

4.  Dopamine D2 receptor expression in the corticotroph cells of the human normal pituitary gland.

Authors:  Rosario Pivonello; Marlijn Waaijers; Johan M Kros; Claudia Pivonello; Cristina de Angelis; Alessia Cozzolino; Annamaria Colao; Steven W J Lamberts; Leo J Hofland
Journal:  Endocrine       Date:  2016-10-13       Impact factor: 3.633

5.  Cabergoline treatment in acromegaly: cons.

Authors:  Leandro Kasuki; Leonardo Vieira Neto; Mônica R Gadelha
Journal:  Endocrine       Date:  2014-02-07       Impact factor: 3.633

Review 6.  Medical therapy in acromegaly.

Authors:  Mark Sherlock; Conor Woods; Michael C Sheppard
Journal:  Nat Rev Endocrinol       Date:  2011-03-29       Impact factor: 43.330

7.  Effectiveness and tolerability of slow release lanreotide treatment in active acromegaly.

Authors:  A Colao; P Marzullo; D Ferone; V Marinò; R Pivonello; C Di Somma; A Di Sarno; A Giaccio; G Lombardi
Journal:  J Endocrinol Invest       Date:  1999-01       Impact factor: 4.256

Review 8.  Somatostatin analogs in medical treatment of acromegaly.

Authors:  Michael S Racine; Ariel L Barkan
Journal:  Endocrine       Date:  2003-04       Impact factor: 3.633

Review 9.  Comparison of efficacy and tolerability of somatostatin analogs and other therapies for acromegaly.

Authors:  Morton G Burt; Ken K Y Ho
Journal:  Endocrine       Date:  2003-04       Impact factor: 3.633

Review 10.  Medical therapy: options and uses.

Authors:  John D Carmichael; Vivien S Bonert
Journal:  Rev Endocr Metab Disord       Date:  2008-03       Impact factor: 6.514

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