Characterisation of a novel porcine coronary artery CTO model

医学 微血管 磁共振成像 冠状动脉 组织学 经皮冠状动脉介入治疗 管腔(解剖学) 动脉 放射科 血管生成 病理 心脏病学 内科学 心肌梗塞
作者
Paul Fefer,Normand Robert,Beiping Qiang,Garry Liu,Nigel R. Munce,Kevan Anderson,Azriel Osherov,Michelle Ladouceur-Wodzak,Xiuling Qi,Alexander Dick,Max Weisbrod,Michelle Samuel,Jagdish Butany,Graham A. Wright,Bradley H. Strauss
出处
期刊:Eurointervention [European Association of Percutaneous Cardiovascular Interventions]
卷期号:7 (12): 1444-1452 被引量:9
标识
DOI:10.4244/eijv7i12a225
摘要

To create a large animal coronary chronic total occlusion (CTO) model. Presence of microvessels within the CTO lumen facilitates guidewire crossing. The patterns and time profiles of matrix changes and microvessel formation during coronary CTO maturation are unknown.CTO were created in 15 swine by percutaneous deployment of a collagen plug. Matrix changes were assessed by histology. Intraluminal neovascularisation was assessed by histology and several imaging modalities, including conventional and 3D spin angiography, micro-computed tomography (micro-CT) imaging, and contrast-enhanced magnetic resonance imaging (MRI), at six and 12 weeks following CTO creation. Matrix changes included an intense inflammatory reaction at six weeks which had partially abated by 12 weeks. A proteoglycan-rich matrix at six weeks was partially replaced with collagen by 12 weeks. Similar changes were noted in the proximal cap which was acellular. Three patterns of microvessel formation were identified and defined based on the presence and extent of a "lead" neovessel. No major differences in pattern or extent of neovascularisation were noted between six and 12 weeks.Heterogeneity in neovascularisation patterns occurs during coronary CTO development in a porcine model. Non-invasive imaging to determine the predominant type of neovascularisation prior to and during CTO revascularisation may improve guidewire crossing success rates. This model may be useful for further exploration of CTO pathophysiology, and may aid in further refinements of in vivo imaging of CTO and development of novel therapeutic approaches to revascularisation of CTO, such as manipulations of the proximal cap, matrix composition, neovessel induction, and device testing.
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