Li Jian-Jun, Zhang Yu-Ping, Wang Chun, Gao Li-Jian, Qin Xue-Wen, Xu Bo, Chen Ji-Lin, Yang Yue-Jin, Gao Run-Lin
Department of Cardiology, Fu Wai Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.
Coron Artery Dis. 2009 Jan;20(1):65-70. doi: 10.1097/MCA.0b013e32830d27bd.
Systemic inflammation after percutaneous coronary intervention (PCI) identifies patients at increased risk of subsequent major adverse cardiac event. During PCI, the technique of stent implantation including direct stenting (DS) and complementary stenting (CS) is guided using both clinical and angiographic features. DS was practiced with increased frequency during PCI in an attempt to reduce both restenosis and major adverse cardiac event in the drug-eluting stent (DES) era. Impact of DS on the early inflammatory response has, however, not been investigated. We hypothesized that a direct DES implantation may attenuate the early inflammatory response compared with CS.
In this study, therefore, we prospectively select the sirolimus-eluting stent (SES) as a model of DESs, and sought to determine the early systemic inflammatory response in patients with single-vessel disease after PCI using either DS or CS techniques.
Thirty-nine patients who had single-vessel disease implanted with SES were randomly enrolled into the two groups: DS group (n=20) or CS group (n=19). The blood samples were taken before PCI, 24 and 72 h after stenting. The plasma concentrations of C-reactive protein and interleukin-6 (IL-6) were determined by enzyme-linked immunosorbent assay.
No significant difference in baseline clinical, angiographic, and inflammatory parameters between the two groups is observed. The plasma IL-6 levels at 24 h after stent implantation were significantly higher than that at baseline in both groups (P<0.05, respectively). Plasma IL-6 level was, however, higher in CS group than in DS group (P<0.01) and was returned to baseline levels in both groups at 72 h after stenting. Meanwhile, the plasma levels of C-reactive protein were also significant higher in CS group compared with DS group at both 24 and 72 h after stenting (P<0.05, respectively).
Taken together, our findings demonstrated that a direct SES implantation significantly attenuated the early systemic inflammatory response in patients with single-vessel disease compared with CS technique.
经皮冠状动脉介入治疗(PCI)后的全身炎症反应可识别出后续发生重大不良心脏事件风险增加的患者。在PCI过程中,支架植入技术包括直接支架置入术(DS)和补充支架置入术(CS),其操作是根据临床和血管造影特征来指导的。在药物洗脱支架(DES)时代,DS在PCI中的应用频率增加,旨在降低再狭窄和重大不良心脏事件的发生率。然而,DS对早期炎症反应的影响尚未得到研究。我们假设与CS相比,直接DES植入可能会减弱早期炎症反应。
因此,在本研究中,我们前瞻性地选择西罗莫司洗脱支架(SES)作为DES的模型,并试图确定采用DS或CS技术进行PCI的单支血管病变患者的早期全身炎症反应。
39名单支血管病变且植入SES的患者被随机分为两组:DS组(n = 20)或CS组(n = 19)。在PCI前以及支架置入后24小时和72小时采集血样。采用酶联免疫吸附测定法测定血浆中C反应蛋白和白细胞介素-6(IL-6)的浓度。
两组在基线临床、血管造影和炎症参数方面未观察到显著差异。两组在支架置入后24小时的血浆IL-6水平均显著高于基线水平(P均<0.05)。然而,CS组的血浆IL-6水平高于DS组(P<0.01),且两组在支架置入后72小时均恢复至基线水平。同时,在支架置入后24小时和72小时,CS组的血浆C反应蛋白水平也显著高于DS组(P均<0.05)。
综上所述,我们的研究结果表明,与CS技术相比,直接SES植入可显著减弱单支血管病变患者的早期全身炎症反应。