@article {AGUILAR-CHAVEZ512, author = {ERIKA A. AGUILAR-CHAVEZ and JORGE I. GAMEZ-NAVA and MARIA A. LOPEZ-OLIVO and SILVIA GALVAN-MELENDRES and ESTHER G. CORONA-SANCHEZ and CARLOS A. LOAIZA-CARDENAS and ALFREDO CELIS and ERNESTO G. CARDONA-MU{\~N}OZ and LAURA GONZALEZ-LOPEZ}, title = {Circulating Leptin and Bone Mineral Density in Rheumatoid Arthritis}, volume = {36}, number = {3}, pages = {512--516}, year = {2009}, doi = {10.3899/jrheum.080196}, publisher = {The Journal of Rheumatology}, abstract = {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{\textquoteright}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{\textquoteright} serum leptin levels varied widely (range 2{\textendash}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.}, issn = {0315-162X}, URL = {https://www.jrheum.org/content/36/3/512}, eprint = {https://www.jrheum.org/content/36/3/512.full.pdf}, journal = {The Journal of Rheumatology} }