Key result
VH-identified TCFA plaques are linked to a ~3.2-fold higher frequency of angioscopic TCFA.
Cross-Sectional (n=57)
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BACKGROUND: Thin cap fibroatheroma (TCFA) is considered to be a vulnerable plaque. Virtual Histology-intravascular ultrasound (VH-IVUS) can precisely identify TCFA in vivo. Intense yellow plaque on angioscopy determined by quantitative colorimetry with L a b color space corresponds with histological TCFA; in particular, a plaque of color b value >23 indicates an atheroma with a fibrous cap thickness <100 mum. In the present study, the relationship between VH-TCFA and angioscopic plaque color determined by colorimetry was investigated. METHODS AND RESULTS: Fifty-seven culprit plaques in 57 patients were evaluated by VH-IVUS and angioscopy. VH-TCFA was defined as a plaque with a necrotic core >10% of plaque area without overlying fibrous tissue, and angioscopic TCFA was a plaque with b value >23. The frequency of angioscopic TCFA was higher in the VH-TCFA group than in the VH-non-TCFA group (74% vs 23%, P=0.0002). Moreover, yellow color intensity (b value) significantly correlated with plaque classification on VH-IVUS. When TCFA detected with angioscopy was used as the gold standard, the sensitivity, specificity, and accuracy for TCFA with VH-IVUS was 68%, 81%, and 75%, respectively. CONCLUSIONS: VH-TCFA strongly correlated with angioscopic TCFA determined by a quantitative analysis with colorimetry.
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Yamamoto et al. (2009) conducted a cross-sectional in Thin cap fibroatheroma / Vulnerable plaque (n=57). Virtual Histology-identified thin cap fibroatheroma (VH-TCFA) vs. Virtual Histology-identified non-TCFA was evaluated on Angioscopic TCFA (plaque of color b value >23) (p=0.0002). Plaques identified as thin cap fibroatheroma (TCFA) by virtual histology had a significantly higher frequency of angioscopic TCFA compared to non-TCFA plaques (74% vs 23%, P=0.0002).
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