Ramonda Roberta, Puato Massimo, Punzi Leonardo, Rattazzi Marcello, Zanon Marta, Balbi Giulia, Ortolan Augusta, Frallonardo Paola, Faggin Elisabetta, Plebani Mario, Zaninotto Martina, Lorenzin Mariagrazia, Pauletto Paolo, Doria Andrea
Rheumatology Unit, Department of Medicine DIMED, University of Padova, Via Giustiniani 2, 35128 Padova, Italy.
Clinica Medica 4, University of Padova, Padova, Italy.
Joint Bone Spine. 2014 Oct;81(5):421-5. doi: 10.1016/j.jbspin.2014.02.005. Epub 2014 Apr 2.
To evaluate the progression of subclinical atherosclerosis in Psoriatic Arthritis (PsA) patients treated with anti-tumor necrosis factor (TNF)-α agents.
Thirty-two PsA patients classified according to the CASPAR criteria and attending the Rheumatology Unit of the University of Padua Medical Center were enrolled in a two-year prospective, observational study. In accordance with the ASAS/EULAR recommendations on the management of these patients, those studied were prescribed biological agents [etanercept (n=21), adalimumab (n=6), infliximab (n=5)]. Plasma lipids, inflammatory biomarkers, including C-reactive protein (CRP), interleukin-6 (IL-6), vessel endothelium growth factor (VEGF), osteoprotegerin (OPG), and TNF-α, as well as Disease Activity Score 28 calculated with CRP (DAS 28-CRP) were evaluated at baseline and after two years of treatment. Bilateral carotid B-mode ultrasound measurements [the mean-intima media thickness (mean-IMT), the mean maximum-IMT (M-Max)] of each carotid artery segment (common, bulb, and internal carotid artery) and the post-occlusion flow-mediated dilation (FMD) of the brachial artery were also assessed at baseline and after two years.
Despite an improvement in the DAS 28-CRP score (P<0.0005) and lower low-density lipoprotein cholesterol (P<0.013) and triglyceride (P<0.036) values, there was a significant progression in both the mean-IMT (P<0.0005) and M-Max (P<0.0005). Moreover, no recovery in FMD (P=ns) was observed after two years of anti TNF-α treatment. Serum TNF-α levels were increased (P=0.003) and OPG values were decreased (P=0.011) at the end of follow- up with respect to baseline values.
Despite improvement in clinical status, arterial remodelling was observed in the PsA patients who were treated with anti TNF-α agents for two years.
评估接受抗肿瘤坏死因子(TNF)-α制剂治疗的银屑病关节炎(PsA)患者亚临床动脉粥样硬化的进展情况。
32例根据CASPAR标准分类且在帕多瓦大学医学中心风湿病科就诊的PsA患者被纳入一项为期两年的前瞻性观察研究。按照ASAS/EULAR关于此类患者管理的建议,为所研究患者开具生物制剂[依那西普(n = 21)、阿达木单抗(n = 6)、英夫利昔单抗(n = 5)]。在基线和治疗两年后评估血脂、炎症生物标志物,包括C反应蛋白(CRP)、白细胞介素-6(IL-6)、血管内皮生长因子(VEGF)、骨保护素(OPG)和TNF-α,以及用CRP计算的疾病活动评分28(DAS 28-CRP)。还在基线和两年后评估每个颈动脉段(颈总动脉、颈动脉球部和颈内动脉)的双侧颈动脉B型超声测量值[平均内膜中层厚度(mean-IMT)、平均最大内膜中层厚度(M-Max)]以及肱动脉闭塞后血流介导的血管舒张功能(FMD)。
尽管DAS 28-CRP评分有所改善(P < 0.0005),低密度脂蛋白胆固醇(P < 0.013)和甘油三酯(P < 0.036)值降低,但mean-IMT(P < 0.0005)和M-Max(P < 0.0005)均有显著进展。此外,抗TNF-α治疗两年后未观察到FMD恢复(P = 无统计学意义)。随访结束时血清TNF-α水平升高(P = 0.003),OPG值降低(P = 0.011),与基线值相比。
尽管临床状况有所改善,但接受抗TNF-α制剂治疗两年的PsA患者出现了动脉重塑。