Cabergoline in acromegaly: a renewed role for dopamine agonist treatment?

Citation
R. Cozzi et al., Cabergoline in acromegaly: a renewed role for dopamine agonist treatment?, EUR J ENDOC, 139(5), 1998, pp. 516-521
Citations number
26
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
EUROPEAN JOURNAL OF ENDOCRINOLOGY
ISSN journal
08044643 → ACNP
Volume
139
Issue
5
Year of publication
1998
Pages
516 - 521
Database
ISI
SICI code
0804-4643(199811)139:5<516:CIAARR>2.0.ZU;2-D
Abstract
Objective and design: Eighteen active acromegalics entered a prospective op en study with cabergoline (CAB), a dopaminergic drug much more potent than bromocriptine (Br). Methods: CAB was administered for 6 months at doses ranging between 0.5mg t wice weekly and 0.5 mg/day. Clinical-anamnestic characteristics of the pati ents were: (i) sensitivity to dopamine agonist drugs (10 patients): (ii) re sistance to somatostatin analogs (SAs) (8 patients); (iii) intolerance to S A (3 patients). In 2 patients marked hyperprolactinemia was present. Results: Basal GH was 6.6 mu g/l (2.2=50) (median (range)), and on treatmen t it was 3.5 mu g/l (1.2-34) (P=0.013). The corresponding IGF-I Values were 720 mu g/l (410-1438) and 375 mu g/l (167-1260) respectively (P=0.00001). Individual GH levels decreased below 2 mu g/l in 5 patients, and between 2 and 5 mu g/l in another 5 patients. IGF-I levels were suppressed below 50% of baseline in 8 patients and normal age-adjusted IGF-I values were reached in 5 patients (27% of the series). The retrospective comparison with previ ous chronic treatment with Br in the 10 suitable patients showed a greater effectiveness of CAB (IGF-I decrease on CAB treatment, 46.8%, on Br treatme nt, 31%, P=0.02). Adenoma shrank in the 3 patients whose pituitary imaging was repeated during CAB. Conclusions: These results envisage that CAB may represent a worthy therape utic tool in acromegalic patients, inducing a degree of IGF-I and GH suppre ssion comparable to SAs, administered by the oral route and much less expen sive.