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维拉帕米或美托洛尔治疗稳定型心绞痛患者的纤溶变量与心血管预后。斯德哥尔摩心绞痛预后研究结果。

Fibrinolytic variables and cardiovascular prognosis in patients with stable angina pectoris treated with verapamil or metoprolol. Results from the Angina Prognosis study in Stockholm.

作者信息

Held C, Hjemdahl P, Rehnqvist N, Wallén N H, Björkander I, Eriksson S V, Forslund L, Wiman B

机构信息

Department of Medicine, Karolinska Hospital, Stockholm, Sweden.

出版信息

Circulation. 1997 May 20;95(10):2380-6. doi: 10.1161/01.cir.95.10.2380.

Abstract

BACKGROUND

Disturbed fibrinolytic function may influence the progression of coronary atherosclerosis and contribute to thrombotic cardiovascular (CV) events.

METHODS AND RESULTS

In the Angina Prognosis Study in Stockholm (APSIS), patients with stable angina pectoris were studied prospectively during double-blind treatment with metoprolol or verapamil. Various measures of fibrinolytic function were studied in 631 (of 809) patients. During a median follow-up time of 3.2 years (2132 patient-years), 32 patients suffered a CV death, 21 had a nonfatal myocardial infarction (MI), and 77 underwent revascularization. Plasma levels of tissue plasminogen activator (TPA) activity and antigen (ag), plasminogen activator inhibitor (PAI-1) activity at test, and TPA responses to exercise were determined at baseline and after 1 month's treatment and were related to subsequent fatal and nonfatal CV events. Univariate Cox regression analysis revealed that elevated levels of TPA-ag at rest (P < .05), high PAI-1 activity (P < .05), and low TPA-ag responses to exercise (P < .05) were associated with increased risk of subsequent CV death. After adjustment for baseline risk factors, TPA-ag independently predicted CV death or MI. In addition, PAI-1 activity independently predicted CV death or MI in male patients. Verapamil treatment was associated with a 10% decrease of TPA-ag levels and metoprolol treatment with a 2% increase (P < .001 for treatment difference).

CONCLUSIONS

Plasma TPA-ag levels at rest, and among male patients PAI-1 activity as well, independently predict subsequent CV death or MI in patients with stable angina pectoris.

摘要

背景

纤维蛋白溶解功能紊乱可能影响冠状动脉粥样硬化的进展,并促使血栓形成性心血管(CV)事件的发生。

方法与结果

在斯德哥尔摩心绞痛预后研究(APSIS)中,对稳定型心绞痛患者在接受美托洛尔或维拉帕米双盲治疗期间进行前瞻性研究。在809例患者中的631例患者中研究了各种纤维蛋白溶解功能指标。在中位随访时间3.2年(2132患者-年)期间,32例患者发生CV死亡,21例发生非致命性心肌梗死(MI),77例接受了血运重建。在基线和治疗1个月后测定血浆组织纤溶酶原激活物(TPA)活性和抗原(ag)、纤溶酶原激活物抑制剂(PAI-1)活性以及TPA对运动的反应,并将其与随后的致命性和非致命性CV事件相关联。单因素Cox回归分析显示,静息时TPA-ag水平升高(P<.05)、PAI-1活性高(P<.05)以及TPA对运动的反应低(P<.05)与随后CV死亡风险增加相关。在对基线危险因素进行调整后,TPA-ag可独立预测CV死亡或MI。此外,PAI-1活性可独立预测男性患者的CV死亡或MI。维拉帕米治疗使TPA-ag水平降低10%,美托洛尔治疗使TPA-ag水平升高2%(治疗差异P<.001)。

结论

静息时血浆TPA-ag水平以及男性患者中的PAI-1活性可独立预测稳定型心绞痛患者随后的CV死亡或MI。

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