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Merck

Leptin and adiponectin as predictors of disease activity in rheumatoid arthritis.

Clinical and experimental rheumatology (2015-05-06)
Daniel-Xavier Xibillé-Friedmann, Eduardo Ortiz-Panozo, Carolina Bustos Rivera-Bahena, Marisol Sandoval-Ríos, Sara-Eugenia Hernández-Góngora, Liliana Dominguez-Hernandez, José-Luis Montiel-Hernández
ABSTRAKT

To assess whether baseline levels of leptin and adiponectin predict disease activity or response to treatment in patients with RA at 6 months, 1 and 2 years of follow-up. A consecutive cohort of patients, classified according to the 2010 ACR/EULAR RA criteria, was evaluated at baseline, 6 months, 1 and 2 years. All were treated with steroids and/or DMARDs. None received biologics. Blood was taken at a baseline to determine plasma anti-CCP, leptin and adiponectin. The relationship between leptin, adiponectin, DAS28 and changes in DAS28 was assessed by multivariable linear and logistic regression from baseline to follow-up. 127 patients completed 6 months, 91 one year and 52 two years of follow-up. All were female, mean age 45 years (18-70), time since onset of disease 7.5 years (0-36). A U-shaped relationship between DAS28 and leptin baseline levels was seen. Adjusting for different factors, leptin levels at baseline predicted higher DAS28 at 6 months and, in patients who were not overweight or obese, predicted disease activity at 6 months, 1 and 2 years. In patients who were not overweight or obese, baseline leptin was able to predict response to treatment at 6 and 12 months. In the short term, baseline leptin levels predict disease activity in all RA patients and response to treatment in RA patients with normal weight.

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Sigma-Aldrich
Leptin from mouse, ≥98% (SDS-PAGE), recombinant, expressed in E. coli, lyophilized powder
Sigma-Aldrich
Leptin from rat, ≥97% (SDS-PAGE), recombinant, expressed in E. coli, lyophilized powder
Sigma-Aldrich
Leptin human, ≥97% (SDS-PAGE), recombinant, expressed in E. coli, lyophilized powder