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Prolactin and autoimmunity: hyperprolactinemia correlates with serositis and anemia in SLE patients.

Authors :
Orbach H
Zandman-Goddard G
Boaz M
Agmon-Levin N
Amital H
Szekanecz Z
Szucs G
Rovensky J
Kiss E
Doria A
Ghirardello A
Gomez-Arbesu J
Stojanovich L
Ingegnoli F
Meroni PL
Rozman B
Blank M
Shoenfeld Y
Source :
Clinical reviews in allergy & immunology [Clin Rev Allergy Immunol] 2012 Apr; Vol. 42 (2), pp. 189-98.
Publication Year :
2012

Abstract

Evidence points to an association of prolactin to autoimmune diseases. We examined the correlation between hyperprolactinemia and disease manifestations and activity in a large patient cohort. Age- and sex-adjusted prolactin concentration was assessed in 256 serum samples from lupus patients utilizing the LIASON prolactin automated immunoassay method (DiaSorin S.p.A, Saluggia, Italy). Disease activity was defined as present if European Consensus Lupus Activity Measurement (ECLAM) > 2 or Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) > 4. Lupus manifestations were grouped by organ involvement, laboratory data, and prescribed medications. Hyperprolactinemia was presented in 46/256 (18%) of the cohort. Hyperprolactinemic patients had significantly more serositis (40% vs. 32.4%, p = 0.03) specifically, pleuritis (33% vs. 17%, p = 0.02), pericarditis (30% vs. 12%, p = 0.002), and peritonitis (15% vs. 0.8%, p = 0.003). Hyperprolactinemic subjects exhibited significantly more anemia (42% vs. 26%, p = 0.02) and marginally more proteinuria (65.5% vs. 46%, p = 0.06). Elevated levels of prolactin were not significantly associated with other clinical manifestations, serology, or therapy. Disease activity scores were not associated with hyperprolactinemia. Hyperprolactinemia in lupus patients is associated with all types of serositis and anemia but not with other clinical, serological therapeutic measures or with disease activity. These results suggest that dopamine agonists may be an optional therapy for lupus patients with hyperprolactinemia.

Details

Language :
English
ISSN :
1559-0267
Volume :
42
Issue :
2
Database :
MEDLINE
Journal :
Clinical reviews in allergy & immunology
Publication Type :
Academic Journal
Accession number :
21287295
Full Text :
https://doi.org/10.1007/s12016-011-8256-0