TY - JOUR T1 - Circulating Leptin and Bone Mineral Density in Rheumatoid Arthritis JF - The Journal of Rheumatology JO - J Rheumatol SP - 512 LP - 516 DO - 10.3899/jrheum.080196 VL - 36 IS - 3 AU - ERIKA A. AGUILAR-CHAVEZ AU - JORGE I. GAMEZ-NAVA AU - MARIA A. LOPEZ-OLIVO AU - SILVIA GALVAN-MELENDRES AU - ESTHER G. CORONA-SANCHEZ AU - CARLOS A. LOAIZA-CARDENAS AU - ALFREDO CELIS AU - ERNESTO G. CARDONA-MUÑOZ AU - LAURA GONZALEZ-LOPEZ Y1 - 2009/03/01 UR - http://www.jrheum.org/content/36/3/512.abstract N2 - Objective. To evaluate the association between circulating leptin and bone mineral density (BMD) in patients with rheumatoid arthritis (RA). Methods. One-hundred thirty postmenopausal women with RA were assessed for body mass index (BMI), disease characteristics, history of drug use, rheumatoid factor, and erythrocyte sedimentation rate (ESR). BMD (g/cm2) was determined in the hip and spine by DEXA. Serum leptin concentrations were measured by ELISA. Spearman’s correlation coefficients (rho) were determined between BMD and leptin and other variables. A multiple regression analysis was used to adjust for confounders. Results. Patients’ serum leptin levels varied widely (range 2–128 ng/ml). Thirty-three patients (25%) had osteoporosis. Higher levels of leptin correlated significantly with BMD in the lumbar spine (rho = 0.17, p = 0.04) and total hip (rho = 0.21, p = 0.01). The variables that were negatively correlated with BMD were age, duration of menopause, and ESR. After adjustment for confounders, leptin was no longer associated with BMD. In the multivariate model, factors that remained associated with BMD in the total hip were age (p = 0.021) and BMI (p = 0.003); and the factors that remained associated with BMD in the lumbar spine were BMI (p = 0.03) and ESR (p = 0.01). Conclusion. No relevant association was found between circulating leptin levels and BMD in patients with RA in this cross-sectional study. Followup studies are needed to evaluate whether abnormal leptin levels confer a risk for fractures due to osteoporosis. ER -