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Atherosclerotic Progression Attenuates the Expression of Nogo-B in Autopsied Coronary Artery: Pathology and Virtual Histology Intravascular Ultrasound Analysis

机译:动脉粥样硬化进展减弱Nogo-B在尸检冠状动脉中的表达:病理学和虚拟组织学血管内超声分析

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摘要

The relation of Nogo-B to atherosclerotic plaque progression is not well understood. Thus, the purpose of this study was to assess the expression of Nogo-B in fibroatheromas (FA) of different stages, classified using virtual histology intravascular ultrasound (VH-IVUS) analysis in 19 autopsied cases of non-sudden cardiac death. VH-IVUS imaging analysis was performed 30 mm from the ostium of each coronary artery. VH-IVUS revealed 11 early FAs (34.5±8.3 yr), 12 late FAs (42.6±16.6 yr), 8 thick-cap FAs (TkCFAs) (46.4±11.1 yr), and 6 thin-cap FAs (TCFAs) (51.8±6.8 yr). TkCFAs and TCFAs were defined as advanced FA. FA progression advanced with age (P=0.04). VH-IVUS analysis of small, early FAs showed smaller necrotic cores and relatively less calcium compared to more advanced FAs with large necrotic cores (P<0.001). Histopathology and immunohistochemical stains demonstrated that early or late FAs had smaller necrotic cores, less empty space of decalcification, and greater Nogo-B expression compared to advanced FAs (vs. early FA, P=0.013; vs. late FA, P=0.008, respectively). These findings suggest that FA progression is inversely associated with Nogo-B expression. Local reduction of Nogo-B may contribute to plaque formation and/or instability.
机译:Nogo-B与动脉粥样硬化斑块进展之间的关系尚不清楚。因此,本研究的目的是评估Nogo-B在不同阶段的纤维状动脉瘤(FA)中的表达,并使用虚拟组织学血管内超声(VH-IVUS)分析对19例非猝死性心脏死亡的尸体进行分类。 VH-IVUS成像分析是在距每个冠状动脉口30 mm处进行的。 VH-IVUS显示11个早期FA(34.5±8.3年),12个晚期FA(42.6±16.6年),8个厚帽FA(TkCFA)(46.4±11.1年)和6个薄帽FA(TCFA)(51.8 ±6.8年)。 TkCFAs和TCFA被定义为高级FA。随着年龄的增长,FA的进展加快(P = 0.04)。与较小的早期FAs相比,VH-IVUS分析显示较小的坏死芯和相对较少的钙(P <0.001)。组织病理学和免疫组织化学染色显示,与晚期FA相比,早期FA或晚期FA具有较小的坏死核心,较少的脱钙空白空间和更大的Nogo-B表达(与早期FA相比,P = 0.013;与晚期FA相比,P = 0.008,分别)。这些发现表明FA进展与Nogo-B表达成反比。 Nogo-B的局部减少可能有助于斑块形成和/或不稳定。

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