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Correlation of Prolactin Serum Concentrations with Clinical Activity and Remission in Patients with Systemic Lupus Erythematosus. Effect of Conventional Treatment
OLGA VERA-LASTRA, CARMEN MENDEZ, LUIS J. JARA, MARTÍN CISNEROS, GABRIELA MEDINA, RAUL ARIZA, and LUIS R. ESPINOZA
ABSTRACT.
Methods. We studied 43 female patients with active SLE, who were divided in 2 groups; Group 1: 16 patients with minor organ involvement (cutaneous and articular involvement), and Group 2: 27 patients with major organ involvement (glomerulonephritis). Controls were 36 healthy individuals. PRL levels were determined by an immunoradiometric assay at entry and after 6 months of treatment. PRL levels were correlated with SLE Disease Activity Index (SLEDAI) score. Results. Mild hyperprolactinemia (HPRL, 20–40 ng/ml) was found in 30/43 (69.7%) SLE patients. After 6 months of treatment a reduction in PRL levels was found in both groups: Group 1: 24.3 ± 10.8 to 16.96 ± 10.87 ng/ml (p < 0.001); and Group 2: 23.6 ± 5.7 to 12.07 ± 11.13 ng/ml (p < 0.001). The SLEDAI score also decreased after treatment: Group 1: 16.5 ± 5.9 to 2.1 ± 1.3 (p < 0.001); Group 2: 16.8 ± 5.4 to 1.6 ± 1.4 (p < 0.001). At entry and after treatment, a significant correlation between PRL levels and SLEDAI score was found in all patients (r = 0.4946, p = 0.0007, and r = 0.9086, p = 0.0001, respectively). Conclusion. HPRL was associated with SLE disease activity. Conventional immunosuppressive therapy decreased PRL levels in direct correlation with decreased SLE activity. This finding emphasizes that PRL may play a role in the pathogenesis and clinical expression of SLE. (J Rheumatol 2003;30:2140-6) Key Indexing Terms:
PROLACTIN
From the Department of Internal Medicine, Clinical Research Unit, Department of Rheumatology, and Department of Epidemiology, Hospital de Especialidades, Centro Medico "La Raza," Mexico City; Hospital General de Zona no. 76, Instituto Mexicano del Seguro Social, Mexico City, Mexico; and the Rheumatology Section, Louisiana State University (LSU), New Orleans, Louisiana, USA. O. Vera-Lastra, MD, Associate Professor of Internal Medicine, Universidad Nacional Autonoma de Mexico (UNAM); C. Mendez, MD, Clinical Research Unit; L.J. Jara, MD, Chief, Clinical Research Unit, Associate Professor of Rheumatology, UNAM; M. Cisneros, MD, MSc; G. Medina, MD, MSc; R. Ariza, MD, Chief, Internal Medicine Department, IMSS, Mexico; L.R. Espinoza, MD, Professor of Medicine, Chief, Rheumatology Section, LSU, USA. Address reprint requests to Dr. L.J. Jara, Clinical Research Unit, Hospital de Especialidades Centro Medico Nacional "La Raza," Seris y Zaachila S/N, Colonia La Raza, CP 02990, Mexico City, Mexico. E-mail: luis_jara_quezada@hotmail.com Submitted May 6, 2002; revision accepted March 28, 2003. |