Zairis Michael N, Papadaki Olga A, Psarogianni Paraskevi K, Thoma Maria A, Andrikopoulos George K, Batika Pelagia C, Poulopoulou Christina G, Trifinopoulou Kyriaki G, Olympios Christopher D, Foussas Stefanos G
Department of Cardiology, Tzanio Hospital, Piraeus, Greece.
Am Heart J. 2003 Dec;146(6):1082-9. doi: 10.1016/S0002-8703(03)00503-9.
Previous studies have shown an incremental role of inflammation in late prognosis following coronary stenting (CS). In particular, high preprocedural levels of plasma C-reactive protein (CRP) have been related to increased hazard of late ischemic complications. Persistent Chlamydia pneumoniae (Cp) infection, detected by positive IgA anti-Cp titers, may be associated with this inflammatory process and portend a high risk of late adverse prognosis after CS.
A total of 483 consecutive patients with either stable or unstable coronary syndromes were followed-up for 1 year after successful CS. The composite of cardiac death, myocardial infarction, rehospitalization for rest-unstable angina, and exertional angina, whichever occurred first, was the clinical end point. Additionally, the rate of in-stent restenosis and progression of coronary artery disease during this period were evaluated. Anti-Cp titers and plasma CRP levels were measured before the procedure.
Positive immunoglobulin A (IgA), but not positive immunoglobulin G (IgG), titers were significantly associated with high plasma CRP levels in patients with unstable coronary syndromes (P =.005), but not in those with stable angina (P =.7). Moreover, positive IgA titers were significantly related to increased risk of both the composite clinical end point (P =.04) and progression of coronary artery disease (P <.001) in patients with unstable coronary syndromes but not in those with stable angina. Neither positive IgA nor positive IgG titers were associated with the rate of in-stent restenosis.
Persistent Cp infection may drive an inflammatory response in the coronary vasculature and portends an adverse late outcome after CS in patients with unstable coronary syndromes.
既往研究表明,炎症在冠状动脉支架置入术(CS)后的远期预后中发挥着越来越重要的作用。特别是,术前血浆C反应蛋白(CRP)水平升高与晚期缺血性并发症风险增加有关。通过IgA抗肺炎衣原体(Cp)滴度阳性检测到的持续性肺炎衣原体(Cp)感染,可能与这一炎症过程相关,并预示着CS术后远期不良预后的高风险。
连续纳入483例稳定或不稳定型冠状动脉综合征患者,在成功进行CS术后随访1年。以首次发生的心源性死亡、心肌梗死、因静息性不稳定型心绞痛或劳力性心绞痛再次住院组成的复合事件为临床终点。此外,评估在此期间支架内再狭窄率和冠状动脉疾病进展情况。术前检测抗Cp滴度和血浆CRP水平。
在不稳定型冠状动脉综合征患者中,免疫球蛋白A(IgA)滴度阳性而非免疫球蛋白G(IgG)滴度阳性与高血浆CRP水平显著相关(P = 0.005),而在稳定型心绞痛患者中则无此相关性(P = 0.7)。此外,在不稳定型冠状动脉综合征患者中,IgA滴度阳性与复合临床终点风险增加(P = 0.04)和冠状动脉疾病进展(P < 0.001)显著相关,而在稳定型心绞痛患者中则无此相关性。IgA和IgG滴度阳性均与支架内再狭窄率无关。
持续性Cp感染可能引发冠状动脉血管的炎症反应,并预示着不稳定型冠状动脉综合征患者CS术后的不良远期结局。