Xibillé-Friedmann Daniel-Xavier, Ortiz-Panozo Eduardo, Bustos Rivera-Bahena Carolina, Sandoval-Ríos Marisol, Hernández-Góngora Sara-Eugenia, Dominguez-Hernandez Liliana, Montiel-Hernández José-Luis
Hospital General de Cuernavaca, SSM/Facultad de Farmacia, UAEM, Morelos, Cuernavaca, Mexico.
Center for Population Health Research, Instituto Nacional de Salud Pública, Cuernavaca, Mexico.
Clin Exp Rheumatol. 2015 Jul-Aug;33(4):471-7. Epub 2015 May 1.
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.
评估瘦素和脂联素的基线水平是否能预测类风湿关节炎(RA)患者在随访6个月、1年和2年时的疾病活动度或治疗反应。
根据2010年美国风湿病学会(ACR)/欧洲抗风湿病联盟(EULAR)的RA标准分类的连续队列患者,在基线、6个月、1年和2年时进行评估。所有患者均接受类固醇和/或改善病情抗风湿药(DMARDs)治疗,无人接受生物制剂治疗。在基线时采集血液以测定血浆抗环瓜氨酸肽(anti-CCP)、瘦素和脂联素。通过多变量线性和逻辑回归评估从基线到随访期间瘦素、脂联素、疾病活动评分28(DAS28)以及DAS28变化之间的关系。
127例患者完成了6个月的随访,91例完成了1年的随访,52例完成了2年的随访。所有患者均为女性,平均年龄45岁(18 - 70岁),病程7.5年(0 - 36年)。观察到DAS28与瘦素基线水平呈U形关系。校正不同因素后,基线瘦素水平可预测6个月时更高的DAS28,在非超重或肥胖患者中,还可预测6个月、1年和2年时的疾病活动度。在非超重或肥胖患者中,基线瘦素能够预测6个月和12个月时的治疗反应。
短期内,基线瘦素水平可预测所有RA患者的疾病活动度以及体重正常的RA患者的治疗反应。