Calcified plaque harboring lipidic materials associates with no-reflow phenomenon after PCI in stable CAD.

IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS International Journal of Cardiovascular Imaging Pub Date : 2023-10-01 Epub Date: 2023-06-28 DOI:10.1007/s10554-023-02905-y
Hayato Hosoda, Yu Kataoka, Stephen J Nicholls, Rishi Puri, Kota Murai, Satoshi Kitahara, Kentaro Mitsui, Hiroki Sugane, Kenichiro Sawada, Takamasa Iwai, Hideo Matama, Satoshi Honda, Kensuke Takagi, Masashi Fujino, Shuichi Yoneda, Fumiyuki Otsuka, Itaru Takamisawa, Kensaku Nishihira, Yasuhide Asaumi, Kazuya Kawai, Teruo Noguchi
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Abstract

Calcified atheroma has been viewed conventionally as stable lesion which less likely increases no-reflow phenomenon. Given that lipidic materials triggers the formation of calcification, lipidic materials could exist within calcified lesion, which may cause no-reflow phenomenon after PCI. The REASSURE-NIRS registry (NCT04864171) employed near-infrared spectroscopy and intravascular ultrasound imaging to evaluate maximum 4-mm lipid-core burden index (maxLCBI4mm) at target lesions containing small (maximum calcification arc < 180°: n = 272) and large calcification (maximum calcification arc ≥ 180°: n = 189) in stable CAD patients. The associations of maxLCBI4mm with corrected TIMI frame count (CTFC) and no-reflow phenomenon after PCI were analyzed in patients with target lesions containing small and large calcification, respectively. No-reflow phenomenon occurred in 8.0% of study population. Receiver-operating characteristics curve analyses revealed that optimal cut-off values of maxLCBI4mm for predicting no-reflow phenomenon were 585 at small calcification (AUC = 0.72, p < 0.001) and 679 at large calcification (AUC = 0.76, p = 0.001). Target lesions containing small calcification with maxLCBI4mm ≥ 585 more likely exhibited a greater CTFC (p < 0.001). In those with large calcification, 55.6% of them had maxLCBI4mm ≥ 400 [vs. 56.2% (small calcification), p = 0.82]. Furthermore, a higher CTFC (p < 0.001) was observed in association with maxLCBI4mm ≥ 679 at large calcification. On multivariable analysis, maxLCBI4mm at large calcification still independently predicted no-reflow phenomenon (OR = 1.60, 95%CI = 1.32-1.94, p < 0.001). MaxLCBI4mm at target lesions exhibiting large calcification elevated a risk of no-reflow phenomenon after PCI. Calcified plaque containing lipidic materials is not necessarily stable lesion, but could be active and high-risk one causing no-reflow phenomenon.

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稳定型CAD患者PCI术后钙化斑块携带脂质物质与无回流现象相关。
钙化性动脉粥样硬化通常被视为稳定的病变,不太可能增加无回流现象。鉴于脂质物质触发钙化的形成,钙化病变内可能存在脂质物质,这可能导致PCI后无回流现象。REASURE-NIRS注册中心(NCT04864171)采用近红外光谱和血管内超声成像来评估包含小(最大钙化弧 分析了在靶病变中分别存在小钙化和大钙化的患者中,4mm具有校正的TIMI帧计数(CTFC)和PCI后无回流现象。8.0%的研究人群中未出现回流现象。受试者操作特征曲线分析显示,在小钙化(AUC = 0.72,p 4毫米 ≥ 585更可能表现出更大的CTFC(p 4毫米 ≥ 400[对56.2%(小钙化),p = 0.82]。此外,较高的CTFC(p 4毫米 ≥ 679在大钙化处。在多变量分析中,大钙化处的maxLCBI4mm仍然独立预测无回流现象(OR = 1.60,95%CI = 1.32-1.94,p 靶病变处出现大钙化的4mm增加了PCI术后无再流现象的风险。含有脂质物质的钙化斑块不一定是稳定的病变,但可能是一种活动性和高风险的病变,导致无回流现象。
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来源期刊
CiteScore
4.00
自引率
9.50%
发文量
77
审稿时长
1 months
期刊介绍: The International Journal of Cardiovascular Imaging publishes technical and clinical communications (original articles, review articles and editorial comments) associated with cardiovascular diseases. The technical communications include the research, development and evaluation of novel imaging methods in the various imaging domains. These domains include magnetic resonance imaging, computed tomography, X-ray imaging, intravascular imaging, and applications in nuclear cardiology and echocardiography, and any combination of these techniques. Of particular interest are topics in medical image processing and image-guided interventions. Clinical applications of such imaging techniques include improved diagnostic approaches, treatment , prognosis and follow-up of cardiovascular patients. Topics include: multi-center or larger individual studies dealing with risk stratification and imaging utilization, applications for better characterization of cardiovascular diseases, and assessment of the efficacy of new drugs and interventional devices.
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