Hyperprolactinemia in males with systemic lupus erythematosus

Citation
Cc. Mok et al., Hyperprolactinemia in males with systemic lupus erythematosus, J RHEUMATOL, 25(12), 1998, pp. 2357-2363
Citations number
44
Categorie Soggetti
Rheumatology,"da verificare
Journal title
JOURNAL OF RHEUMATOLOGY
ISSN journal
0315162X → ACNP
Volume
25
Issue
12
Year of publication
1998
Pages
2357 - 2363
Database
ISI
SICI code
0315-162X(199812)25:12<2357:HIMWSL>2.0.ZU;2-0
Abstract
Objective. To study prospectively the serum prolactin (PRL) concentrations among male patients with systemic lupus erythematosus (SLE) and their possi ble relationship to disease activity and manifestations. Methods, Serum PRL levels were measured by radioimmunoassay in 31 male pati ents with SLE and 31 age matched controls. Demographic, clinical, and labor atory features of the patients were obtained. Mean PRL levels from both gro ups were compared, and PRL from patients with SLE was correlated with varia bles of disease activity, including the SLE Disease Activity Index (SLEDAI) , complement level, and anti-dsDNA titer. Thirteen patients were followed s erially and changes in PRL levels in relation to fluctuation in disease act ivity were evaluated. Results. Mean PRL levels were higher in male patients with SLE than healthy controls; however, the difference did not reach statistical significance ( 230 vs 194 mIU/l; p = 0.06). Hyperprolactinemia was found in 4 patients (13 %) and was not associated with particular clinical manifestations or autoan tibodies. Considering all patients as a whole, PRL levels did not correlate with variables of disease activity and there was no difference in PRL betw een patients with active versus inactive disease. A subanalysis of the 4 hy perprolactinemic patients revealed a higher SLEDAI score than those with no rmal PRL (8.8 vs 3.7; p = 0.20); however, the difference was not statistica lly significant. Among the hyperprolactinemic patients, PRL levels did not correlate with SLEDAI score or anti-dsDNA titer. Prospective studies of PRL levels in 13 patients did not indicate a role of PRL in the monitoring of disease activity or predicting relapses. Conclusion. Hyperprolactinemia occurred in a small proportion of male patie nts with SLE and its significance remained unclear. Serum PRL level did not correlate with disease activity and was not a reliable marker for disease monitoring.