Preprocedural inflammatory markers do not predict restenosis after successful coronary stenting

被引:42
作者
Gomma, AH
Hirschfield, GM
Gallimore, JR
Lowe, GDO
Pepys, MB
Fox, KM
机构
[1] Royal Brompton Hosp, Dept Cardiol, London SW3 6NP, England
[2] Natl Heart & Lung Inst, Dept Cardiol, London, England
[3] UCL Royal Free & Univ Coll, Sch Med, Ctr Amyloidosis & Acute Phase Prot, Dept Med, London, England
[4] Univ Glasgow, Royal Infirm, Dept Med, Glasgow G31 2ER, Lanark, Scotland
关键词
D O I
10.1016/j.ahj.2003.10.050
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Levels of C-reactive protein (CRP), serum amyloid A protein (SAA), and interleukin-6 (IL-6) can predict coronary restenosis following angioplasty and stent deployment in patients with unstable angina. We investigated whether measurement of periprocedural inflammatory markers predicted the angiographic outcome at 6 months in stable angina patients undergoing coronary stenting. Methods We prospectively studied 182 patients; 152 patients underwent elective and successful stenting procedure. for de novo lesions in native and nongrafted coronary arteries and 30 individuals in the control group underwent diagnostic angiography alone. CRP, SAA, and IL-6 were determined by high-sensitivity immunoassays. Results At 6 months, quantitative computer-assisted angiographic analysis in 133 patients with stents showed a binary restenosis rate of 33.8%. Statins were being taken by 80% of the patients. There were no significant differences between the pre- or postprocedure values of CRP, SAA, or IL-6 in patients with or without in-stent restenosis. Conclusions Preprocedural inflammatory markers in stable angina subjects undergoing coronary artery stent deployment did not correlate with the development of in-stern restenosis. Differences in pathobiology between stable and unstable coronary syndromes, the widespread use of statins with anti-inflammatory activity in our cohort of patients, along with different mechanisms underlying the early angiographic appearances of restenosis as compared to clinical end points, most likely explain our findings.
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页码:1071 / 1077
页数:7
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