Rodriguez-Jimenez Norma Alejandra, Garcia-Gonzalez Carlos E, Ayala-Lopez Karina Patricia, Trujillo-Hernandez Benjamin, Aguilar-Chavez Erika Anita, Rocha-Muñoz Alberto Daniel, Vasquez-Jimenez Jose Clemente, Olivas-Flores Eva, Salazar-Paramo Mario, Corona-Sanchez Esther Guadalupe, Vazquez-Del Mercado Monica, Varon-Villalpando Evangelina, Cota-Sanchez Adolfo, Cardona-Muñoz Ernesto German, Gamez-Nava Jorge I, Gonzalez-Lopez Laura
Programa de Doctorado en Farmacologia, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara (U de G), Guadalajara, JAL, Mexico.
Hospital de Especialidades, Centro Medico Nacional de Occidente, Instituto Mexicano del Seguro Social (IMSS), Guadalajara, JAL, Mexico.
Biomed Res Int. 2014;2014:510305. doi: 10.1155/2014/510305. Epub 2014 Aug 27.
To compare the modifications in lipids between patients with rheumatoid arthritis (RA) receiving etanercept plus methotrexate (ETA + MTX) versus methotrexate (MTX) and their relationship with serum levels of tumor necrosis factor-alpha (TNF-α).
In an observational cohort study, we compared changes in lipid levels in patients receiving ETA + MTX versus MTX in RA. These groups were assessed at baseline and at 4 and 24 weeks, measuring clinical outcomes, total cholesterol, triglycerides, high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol, and TNF-α.
Baseline values for lipid levels were similar in both groups. HDL-C levels increased significantly only in the ETA + MTX group (from 45.5 to 50.0 mg/dL at 4 weeks, a 10.2% increase, P < 0.001, and to 56.0 mg/dL at 24 weeks, a 25.1% increase, P < 0.001), while other lipids underwent no significant changes. ETA + MTX also exhibited a significant increase in TNF-α (44.8 pg/mL at baseline versus 281.4 pg/mL at 24 weeks, P < 0.001). The MTX group had no significant changes in lipids or TNF-α. Significant differences in HDL-C between groups were observed at 24 weeks (P = 0.04) and also in TNF-α (P = 0.01).
HDL-C levels increased significantly following treatment with ETA + MTX, without a relationship with decrease of TNF-α.
比较接受依那西普联合甲氨蝶呤(ETA+MTX)治疗的类风湿关节炎(RA)患者与接受甲氨蝶呤(MTX)治疗的患者血脂的变化情况,以及它们与血清肿瘤坏死因子-α(TNF-α)水平的关系。
在一项观察性队列研究中,我们比较了RA患者接受ETA+MTX治疗与接受MTX治疗时血脂水平的变化。在基线、4周和24周时对这些组进行评估,测量临床结局、总胆固醇、甘油三酯、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇和TNF-α。
两组血脂水平的基线值相似。仅ETA+MTX组的HDL-C水平显著升高(4周时从45.5mg/dL升至50.0mg/dL,升高10.2%,P<0.001;24周时升至56.0mg/dL,升高25.1%,P<0.001),而其他血脂无显著变化。ETA+MTX组的TNF-α也显著升高(基线时为44.8pg/mL,24周时为281.4pg/mL,P<0.001)。MTX组的血脂和TNF-α无显著变化。两组在24周时HDL-C有显著差异(P=0.04),TNF-α也有显著差异(P=0.01)。
ETA+MTX治疗后HDL-C水平显著升高,与TNF-α降低无关。