Arbustini E, De Servi S, Bramucci E, Porcu E, Costante A M, Grasso M, Diegoli M, Fasani R, Morbini P, Angoli L, Boscarini M, Repetto S, Danzi G, Niccoli L, Campolo L, Lucreziotti S, Specchia G
Pathology Department, IRCCS Policlinico S. Matteo, University of Pavia, Italy.
Am J Cardiol. 1995 Apr 1;75(10):675-82. doi: 10.1016/s0002-9149(99)80652-3.
The present study investigated the incidence of the histopathologic lesions and of growth factor expression in a consecutive series of directional coronary atherectomy (DCA) samples from 40 unstable angina pectoris patients without prior acute myocardial infarction and compared the findings with those obtained in DCA samples from 18 patients with stable angina without previous infarction and 18 patients with restenosis. We investigated coronary thrombosis, neointimal hyperplasia, and inflammation. For unstable angina, we correlated the angiographic Ambrose plaque subtypes with the histopathologic findings. The immunophenotype of plaque cells and the growth factor expression were assessed with specific antibodies for cell characterization and for the expression of basic fibroblast and platelet-derived AA and AB growth factors and receptors. The incidence of coronary thrombosis was 35% in patients with unstable angina, 17% in those with stable angina, and 11% in patients with restenosis. Neointimal hyperplasia was found in 38% of unstable angina cases, in 17% of stable angina cases, and in 83% of restenosis cases. Inflammation without thrombus or accelerated progression occurred in 20% of unstable angina and 6% of stable angina samples. In 52% of unstable angina cases, inflammation coexisted with thrombosis and/or neointimal hyperplasia. In the unstable angina group, 71% of the plaques with thrombus had a corresponding angiographic pattern of complicated lesions. The growth factor expression, reported as percentage of cells immunostaining with different growth factor antibodies, was highest in restenosis, followed by unstable angina and stable angina lesions.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究调查了40例无既往急性心肌梗死的不稳定型心绞痛患者连续系列定向冠状动脉斑块旋切术(DCA)样本中的组织病理学病变及生长因子表达发生率,并将结果与18例无既往梗死的稳定型心绞痛患者及18例再狭窄患者的DCA样本结果进行比较。我们研究了冠状动脉血栓形成、内膜增生和炎症。对于不稳定型心绞痛,我们将血管造影的安布罗斯斑块亚型与组织病理学结果相关联。用特异性抗体评估斑块细胞的免疫表型及生长因子表达,以进行细胞表征以及检测碱性成纤维细胞生长因子、血小板衍生生长因子AA和AB及其受体的表达。不稳定型心绞痛患者冠状动脉血栓形成的发生率为35%,稳定型心绞痛患者为17%,再狭窄患者为11%。内膜增生在38%的不稳定型心绞痛病例、17%的稳定型心绞痛病例以及83%的再狭窄病例中被发现。无血栓或进展加速的炎症在20%的不稳定型心绞痛样本和6%的稳定型心绞痛样本中出现。在52%的不稳定型心绞痛病例中,炎症与血栓形成和/或内膜增生并存。在不稳定型心绞痛组中,71%有血栓的斑块具有相应的血管造影复杂病变模式。生长因子表达以用不同生长因子抗体免疫染色的细胞百分比表示,在再狭窄中最高,其次是不稳定型心绞痛和稳定型心绞痛病变。(摘要截选至250词)