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采用连续虚拟组织学血管内超声组织特征技术评估冠状动脉病变形态的动态变化。

The dynamic nature of coronary artery lesion morphology assessed by serial virtual histology intravascular ultrasound tissue characterization.

机构信息

Cardiovascular Research Foundation, New York, New York 10022, USA.

出版信息

J Am Coll Cardiol. 2010 Apr 13;55(15):1590-7. doi: 10.1016/j.jacc.2009.07.078.

Abstract

OBJECTIVES

We used virtual histology intravascular ultrasound (VH-IVUS) to investigate the natural history of coronary artery lesion morphology.

BACKGROUND

Plaque stability is related to its histological composition.

METHODS

We performed serial (baseline and 12-month follow-up) VH-IVUS studies and examined 216 nonculprit lesions (plaque burden >or=40%) in 99 patients. Lesions were classified into pathological intimal thickening (PIT), VH-IVUS-derived thin-capped fibroatheroma (VH-TCFA), thick-capped fibroatheroma (ThCFA), fibrotic plaque, and fibrocalcific plaque.

RESULTS

At baseline, 20 lesions were VH-TCFAs; during follow-up, 15 (75%) VH-TCFAs "healed," 13 became ThCFAs, 2 became fibrotic plaque, and 5 (25%) VH-TCFAs remained unchanged. Compared with VH-TCFAs that healed, VH-TCFAs that remained VH-TCFAs located more proximally (values are median [interquartile range]) (16 mm [15 to 18 mm] vs. 31 mm [22 to 47 mm], p = 0.013) and had larger lumen (9.1 mm(2) [8.2 to 10.7 mm(2)] vs. 6.9 mm(2) [6.0 to 8.2 mm(2)], p = 0.021), vessel (18.7 mm(2) [17.3 to 28.6 mm(2)] vs. 15.5 mm(2) [13.3 to 16.6 mm(2)]; p = 0.010), and plaque (9.7 mm(2) [9.6 to 15.7 mm(2)] vs. 8.4 mm(2) [7 to 9.7 mm(2)], p = 0.027) areas; however, baseline VH-IVUS plaque composition did not differ between VH-TCFAs that healed and VH-TCFAs that remained VH-TCFAs. Conversely, 12 new VH-TCFAs developed; 6 late-developing VH-TCFAs were PITs, and 6 were ThCFAs at baseline. In addition, plaque area at minimum lumen sites increased significantly in PITs (7.8 mm(2) [6.2 to 10.0 mm(2)] to 9.0 mm(2) [6.5 to 12.0 mm(2)], p < 0.001), VH-TCFAs (8.6 mm(2) [7.3 to 9.9 mm(2)] to 9.5 mm(2) [7.8 to 10.8 mm(2)], p = 0.024), and ThCFAs (8.6 mm(2) [6.8 to 10.2 mm(2)] to 8.8 mm(2) [7.1 to 11.4 mm(2)], p < 0.001) with a corresponding decrease lumen areas, but not in fibrous or fibrocalcific plaque.

CONCLUSIONS

Most VH-TCFAs healed during 12-month follow-up, whereas new VH-TCFAs also developed. PITs, VH-TCFAs, and ThCFAs showed significant plaque progression compared with fibrous and fibrocalcific plaque.

摘要

目的

我们使用虚拟组织学血管内超声(VH-IVUS)来研究冠状动脉病变形态的自然史。

背景

斑块稳定性与其组织学组成有关。

方法

我们对 99 例患者的 216 个非罪犯病变(斑块负担≥40%)进行了连续(基线和 12 个月随访)VH-IVUS 研究,并对其进行了检查。病变分为病理性内膜增厚(PIT)、VH-IVUS 衍生的薄帽纤维粥样瘤(VH-TCFA)、厚帽纤维粥样瘤(ThCFA)、纤维斑块和纤维钙化斑块。

结果

基线时有 20 个病变为 VH-TCFAs;随访期间,15 个(75%)VH-TCFAs“愈合”,13 个成为 ThCFAs,2 个成为纤维斑块,5 个(25%)VH-TCFAs保持不变。与愈合的 VH-TCFAs 相比,仍为 VH-TCFAs 的病变位于更近端(数值为中位数[四分位数范围])(16mm[15-18mm] vs. 31mm[22-47mm],p=0.013),管腔更大(9.1mm2[8.2-10.7mm2] vs. 6.9mm2[6.0-8.2mm2],p=0.021),血管(18.7mm2[17.3-28.6mm2] vs. 15.5mm2[13.3-16.6mm2],p=0.010)和斑块(9.7mm2[9.6-15.7mm2] vs. 8.4mm2[7-9.7mm2],p=0.027)面积也更大;然而,愈合的 VH-TCFAs 和未愈合的 VH-TCFAs 的基线 VH-IVUS 斑块组成没有差异。相反,又出现了 12 个新的 VH-TCFAs;其中 6 个新发的 VH-TCFAs 为 PIT,6 个为基线时的 ThCFA。此外,PIT 最小管腔部位的斑块面积显著增加(7.8mm2[6.2-10.0mm2]至 9.0mm2[6.5-12.0mm2],p<0.001),VH-TCFAs(8.6mm2[7.3-9.9mm2]至 9.5mm2[7.8-10.8mm2],p=0.024)和 ThCFAs(8.6mm2[6.8-10.2mm2]至 8.8mm2[7.1-11.4mm2],p<0.001),同时管腔面积减小,但纤维或纤维钙化斑块则没有。

结论

大多数 VH-TCFAs 在 12 个月的随访中愈合,而新的 VH-TCFAs 也在发展。与纤维和纤维钙化斑块相比,PIT、VH-TCFAs 和 ThCFAs 显示出明显的斑块进展。

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