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Dopamine D2 receptor gene polymorphisms and response to cabergoline therapy in patients with prolactin-secreting pituitary adenomas.

Authors :
Filopanti, M.
Barbieri, A. M.
Angioni, A. R.
Colao, A.
Gasco, V.
Grottoli, S.
Peri, A.
Baglioni, S.
Fustini, M. F.
Pigliaru, F.
Monte, P. D.
Borretta, G.
Ambrosi, B.
Jaffrain-Rea, M. L.
Gasperi, M.
Brogioni, S.
Cannavò, S.
Mantovani, G.
Beck-Peccoz, P.
Lania, A.
Source :
Pharmacogenomics Journal. 2008, Vol. 8 Issue 5, p357-363. 7p. 3 Charts.
Publication Year :
2008

Abstract

Dopamine-agonist cabergoline (CB) reduces prolactin (PRL) secretion and tumor size in 80% of patients with prolactin-secreting adenomas (PRL-omas) by binding type 2 dopamine receptor (DRD2). The mechanisms responsible for resistance to CB remain largely unknown. To assess the association of DRD2 with sensitivity to CB, TaqI-A1/A2, TaqI-B1/B2, HphI-G/T and NcoI-C/T genotypes were determined in a cross-sectional retrospective study, including 203 patients with PRL-oma. DRD2 alleles frequencies did not differ between patients and 212 healthy subjects. Conversely, NcoI-T allele frequency was higher in resistant rather than responsive patients, considering both PRL normalization (56.6 vs 45.3%, P=0.038) and tumor shrinkage (70.4 vs 41.4%, P=0.006). Finally, [TaqI A1−/TaqI B1−/HphI T−/NcoI T−] haplotype was found in 34.5% of patients normalizing PRL with 3 mg/week of CB vs 11.3% of resistants (P=0.021). In conclusion, resistance to CB was associated with DRD2 NcoI-T+ allele, consistent with evidence suggesting that this variant may lead to reduction and instability of DRD2 mRNA or protein.The Pharmacogenomics Journal (2008) 8, 357–363; doi:10.1038/tpj.2008.1; published online 11 March 2008 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1470269X
Volume :
8
Issue :
5
Database :
Academic Search Index
Journal :
Pharmacogenomics Journal
Publication Type :
Academic Journal
Accession number :
34360187
Full Text :
https://doi.org/10.1038/tpj.2008.1