Effect of long-term cabergoline therapy on the immunological pattern and pituitary function of patients with idiopathic hyperprolactinaemia positive for antipituitary antibodies

被引:10
作者
De Bellis, A. [1 ]
Colao, A. [2 ]
Savoia, A. [1 ]
Coronella, C. [1 ]
Pasquali, D. [1 ]
Conte, M. [1 ]
Pivonello, R. [2 ]
Bellastella, A. [1 ]
Sinisi, A. A. [1 ]
Bizzarro, A. [1 ]
Lombardi, G. [2 ]
Bellastella, G. [1 ]
机构
[1] Univ Naples 2, Dept Clin & Expt Med & Surg, I-80131 Naples, Italy
[2] Univ Naples Federico II, Dept Mol & Clin Endocrinol & Oncol, Naples, Italy
关键词
D O I
10.1111/j.1365-2265.2008.03200.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective The occurrence of antipituitary antibodies (APA) in patients with idiopathic hyperprolactinaemia (IH) and the effects of dopamine agonists on these antibodies and long-term pituitary function outcome have been so far not evaluated. This longitudinal study was aimed at investigating, in patients with IH the occurrence of APA and the effect of cabergoline on the pituitary function and behaviour of APA. Design Sixty-six patients with IH were studied. APA (by indirect immunofluorescence) and pituitary function were investigated every year for 3 years. Results Seventeen patients resulted APA positive (Group 1) and 49 APA negative (Group 2). Eight patients of Group 1 (Group 1a) and 24 of Group 2 (Group 2a) were asymptomatic and then not treated; instead, nine patients in Group 1 (Group 1b) and 25 in Group 2 (Group 2b), showing symptoms of hyperprolactinaemia, were treated with cabergoline for 2 years. Among the untreated patients, during the follow-up, those with APA positive (Group 1a) showed an increase of APA titres and PRL levels with partial pituitary impairment in some of them; instead those with APA negative (Group 2a) persisted negative with normal pituitary function despite persistent hyperprolactinaemia. Among the treated patients, those with APA positive (Group 1b) showed normalization of PRL levels, APA disappearance and recovery of pituitary function (when initially impaired) during cabergoline treatment, persisting also at last observation (off-therapy). Instead all patients of Group 2b persisted with APA negative during the follow-up with normalization of PRL levels and stable normal pituitary function during cabergoline therapy but showing a further increase of PRL at the last observation. Conclusions The presence of APA in some patients with IH suggests a possible occurrence of autoimmune hypophysitis at potential/subclinical stage; an early and prolonged cabergoline therapy could interrupt the progression to an overt clinical stage of the disease. However, the small amount of patients investigated suggests caution against generalization of our assumption and prompts to further controlled studies on a more numerous population to verify these conclusions.
引用
收藏
页码:285 / 291
页数:7
相关论文
共 45 条
[1]   Bromocriptine in systemic lupus erythematosus: a double-blind, randomized, placebo-controlled study [J].
Alvarez-Nemegyei, J ;
Cobarrubias-Cobos, A ;
Escalante-Triay, F ;
Sosa-Munoz, J ;
Miranda, JM ;
Jara, LJ .
LUPUS, 1998, 7 (06) :414-419
[2]   Prolactin secretion is increased in patients with multiple sclerosis [J].
Azar, ST ;
Yamout, B .
ENDOCRINE RESEARCH, 1999, 25 (02) :207-214
[4]   Lymphocytic hypophysitis: a rare or underestimated disease? [J].
Bellastella, A ;
Bizzarro, A ;
Coronella, C ;
Bellastella, G ;
Sinisi, AA ;
De Bellis, A .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2003, 149 (05) :363-376
[5]   Extrapituitary prolactin: Distribution, regulation, functions, and clinical aspects [J].
BenJonathan, N ;
Mershon, JL ;
Allen, DL ;
Steinmetz, RW .
ENDOCRINE REVIEWS, 1996, 17 (06) :639-669
[6]   Prolactin (PRL) and its receptor: Actions, signal transduction pathways and phenotypes observed in PRL receptor knockout mice [J].
Bole-Feysot, C ;
Goffin, V ;
Edery, M ;
Binart, N ;
Kelly, PA .
ENDOCRINE REVIEWS, 1998, 19 (03) :225-268
[7]   Guidelines of the Pituitary Society for the diagnosis and management of prolactinomas [J].
Casanueva, Felipe F. ;
Molitch, Mark E. ;
Schlechte, Janet A. ;
Abs, Roger ;
Bonert, Vivien ;
Bronstein, Marcello D. ;
Brue, Thierry ;
Cappabianca, Paolo ;
Colao, Annamaria ;
Fahlbusch, Rudolf ;
Fideleff, Hugo ;
Hadani, Moshe ;
Kelly, Paul ;
Kleinberg, David ;
Laws, Edward ;
Marek, Josef ;
Scanlon, Maurice ;
Sobrinho, Luis G. ;
Wass, John A. H. ;
Giustina, Andrea .
CLINICAL ENDOCRINOLOGY, 2006, 65 (02) :265-273
[8]   Autoimmune hypophysitis [J].
Caturegli, P ;
Newschaffer, C ;
Olivi, A ;
Pomper, MG ;
Burger, PC ;
Rose, NR .
ENDOCRINE REVIEWS, 2005, 26 (05) :599-614
[9]   The spectrum and significance of primary hypophysitis [J].
Cheung, CC ;
Ezzat, S ;
Smyth, HS ;
Asa, SL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (03) :1048-1053
[10]  
CHIKANZA IC, 1993, BRIT J RHEUMATOL, V32, P445