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本文引用的文献

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Update of the Mexican College of Rheumatology guidelines for the pharmacologic treatment of rheumatoid arthritis.墨西哥风湿病学会类风湿关节炎药物治疗指南更新
Reumatol Clin. 2014 Jul-Aug;10(4):227-40. doi: 10.1016/j.reuma.2013.10.006. Epub 2013 Dec 14.
2
Pro-atherogenic lipid changes and decreased hepatic LDL receptor expression by tocilizumab in rheumatoid arthritis.托珠单抗在类风湿关节炎患者中致动脉粥样硬化脂质变化和肝脏 LDL 受体表达降低。
Atherosclerosis. 2013 Jul;229(1):174-81. doi: 10.1016/j.atherosclerosis.2013.04.031. Epub 2013 May 11.
3
Metabolic syndrome in rheumatoid arthritis.类风湿关节炎的代谢综合征。
Mediators Inflamm. 2013;2013:710928. doi: 10.1155/2013/710928. Epub 2013 Jan 30.
4
The APOM polymorphism as a novel risk factor for dyslipidaemia in rheumatoid arthritis: a possible shared link between disease susceptibility and dyslipidaemia.APOM 多态性作为类风湿关节炎血脂异常的新的危险因素:疾病易感性和血脂异常之间可能存在共同联系。
Clin Exp Rheumatol. 2013 Mar-Apr;31(2):180-8. Epub 2012 Nov 28.
5
Anti-TNF-alpha-adalimumab therapy is associated with persistent improvement of endothelial function without progression of carotid intima-media wall thickness in patients with rheumatoid arthritis refractory to conventional therapy.抗 TNF-α-阿达木单抗治疗与内皮功能的持续改善相关,而不会导致常规治疗抵抗的类风湿关节炎患者颈动脉内膜中层厚度进展。
Mediators Inflamm. 2012;2012:674265. doi: 10.1155/2012/674265. Epub 2012 Jul 31.
6
NFKB1-94ATTG ins/del polymorphism (rs28362491) is associated with cardiovascular disease in patients with rheumatoid arthritis.核因子κB1-94ATTG 插入/缺失多态性(rs28362491)与类风湿关节炎患者的心血管疾病相关。
Atherosclerosis. 2012 Oct;224(2):426-9. doi: 10.1016/j.atherosclerosis.2012.06.008. Epub 2012 Jun 13.
7
The safety and efficacy of etanercept on cardiac functions and lipid profile in patients with active rheumatoid arthritis.依那西普对活动期类风湿关节炎患者心脏功能和血脂谱的安全性和疗效。
J Investig Med. 2012 Jan;60(1):62-5. doi: 10.2310/JIM.0b013e31823a00f4.
8
Glucocorticoids and cardiovascular risk factors.糖皮质激素与心血管危险因素。
Endocrinol Metab Clin North Am. 2011 Jun;40(2):409-17, ix. doi: 10.1016/j.ecl.2011.01.011.
9
TNFA -308 (rs1800629) polymorphism is associated with a higher risk of cardiovascular disease in patients with rheumatoid arthritis.肿瘤坏死因子-α-308(rs1800629)多态性与类风湿关节炎患者发生心血管疾病的风险增加相关。
Atherosclerosis. 2011 May;216(1):125-30. doi: 10.1016/j.atherosclerosis.2010.10.052. Epub 2011 Feb 24.
10
Should both HDL-C and LDL-C be targets for lipid therapy? A review of current evidence.是否应该将 HDL-C 和 LDL-C 都作为降脂治疗的目标?对当前证据的综述。
J Clin Lipidol. 2007 Mar;1(1):88-94. doi: 10.1016/j.jacl.2007.02.004. Epub 2007 Feb 15.

类风湿关节炎患者血脂水平的改变与血清肿瘤坏死因子-α无关:一项为期24周的观察性队列研究结果,该研究比较了接受依那西普联合甲氨蝶呤或甲氨蝶呤单药治疗的患者。

Modifications in lipid levels are independent of serum TNF-α in rheumatoid arthritis: results of an observational 24-week cohort study comparing patients receiving etanercept plus methotrexate or methotrexate as monotherapy.

作者信息

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

机构信息

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.

出版信息

Biomed Res Int. 2014;2014:510305. doi: 10.1155/2014/510305. Epub 2014 Aug 27.

DOI:10.1155/2014/510305
PMID:25243145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4160615/
Abstract

OBJECTIVE

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).

METHODS

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.

RESULTS

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).

CONCLUSION

HDL-C levels increased significantly following treatment with ETA + MTX, without a relationship with decrease of TNF-α.

摘要

目的

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。

方法

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。

结果

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)。

结论

ETA+MTX治疗后HDL-C水平显著升高,与TNF-α降低无关。