Molecular Coronary Plaque Imaging Using 18F-Fluoride.

IF 1.9 4区 物理与天体物理 Q2 BIOLOGY Origins of Life and Evolution of Biospheres Pub Date : 2019-08-01 Epub Date: 2019-08-06 DOI:10.1161/CIRCIMAGING.118.008574
Alastair J Moss, Mhairi K Doris, Jack P M Andrews, Rong Bing, Marwa Daghem, Edwin J R van Beek, Laura Forsyth, Anoop S V Shah, Michelle C Williams, Stephanie Sellers, Jonathon Leipsic, Marc R Dweck, Richard A Parker, David E Newby, Philip D Adamson
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Abstract

Background: Coronary 18F-fluoride positron emission tomography identifies ruptured and high-risk atherosclerotic plaque. The optimal method to identify, to quantify, and to categorize increased coronary 18F-fluoride uptake and determine its reproducibility has yet to be established. This study aimed to optimize the identification, quantification, categorization, and scan-rescan reproducibility of increased 18F-fluoride activity in coronary atherosclerotic plaque.

Methods: In a prospective observational study, patients with multi-vessel coronary artery disease underwent serial 18F-fluoride positron emission tomography. Coronary 18F-fluoride activity was visually assessed, quantified, and categorized with reference to maximal tissue to background ratios. Levels of agreement for both visual and quantitative methods were determined between scans and observers.

Results: Thirty patients (90% male, 20 patients with stable coronary artery disease, and 10 with recent type 1 myocardial infarction) underwent paired serial positron emission tomography-coronary computed tomography angiography imaging within an interval of 12±5 days. A mean of 3.7±1.8 18F-fluoride positive plaques per patient was identified after recent acute coronary syndrome, compared with 2.4±2.3 positive plaques per patient in stable coronary artery disease. The bias in agreement in maximum tissue to background ratio measurements in visually positive plaques was low between observers (mean difference, -0.01; 95% limits of agreement, -0.32 to 0.30) or between scans (mean difference, 0.06; 95% limits of agreement, -0.49 to 0.61). Good agreement in the categorization of focal 18F-fluoride uptake was achieved using visual assessment alone (κ=0.66) and further improved at higher maximum tissue to background ratio values.

Conclusions: Coronary 18F-fluoride activity is a precise and reproducible metric in the coronary vasculature. The analytical performance of 18F-fluoride is sufficient to assess the prognostic utility of this radiotracer as a noninvasive imaging biomarker of plaque vulnerability.

Clinical trial registration: URL: http://www.clinicaltrials.gov. Unique identifiers: NCT02110303 and NCT02278211.

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18f -氟化物在冠状动脉斑块分子成像中的应用
背景:冠状动脉18f -氟化物正电子发射断层扫描识别破裂和高风险的动脉粥样硬化斑块。确定、量化和分类冠状动脉18f -氟化物摄取增加并确定其可重复性的最佳方法尚未建立。本研究旨在优化冠状动脉粥样硬化斑块中18f -氟化物活性升高的鉴定、定量、分类和扫描扫描的可重复性。方法:在一项前瞻性观察研究中,对多支冠状动脉疾病患者进行了系列18f -氟化物正电子发射断层扫描。冠状动脉18f -氟化物活性被目视评估、量化,并参照最大组织与背景比率进行分类。在扫描者和观察者之间确定了视觉和定量方法的一致程度。结果:30例患者(90%为男性,20例为稳定型冠状动脉疾病,10例为新近发生的1型心肌梗死)在12±5天的间隔内接受了配对序列正电子发射断层扫描-冠状动脉计算机断层扫描血管造影成像。近期急性冠状动脉综合征患者平均发现3.7±1.8个18f -氟化物阳性斑块,而稳定型冠状动脉疾病患者平均发现2.4±2.3个阳性斑块。在观察者之间,视觉阳性斑块的最大组织与背景比值测量结果的一致性偏差很低(平均差值为-0.01;95%的一致性界限,-0.32至0.30)或扫描之间(平均差,0.06;95%一致性限,-0.49至0.61)。单独使用视觉评估(κ=0.66)对局灶18f -氟化物摄取的分类达成了良好的一致性,并且在更高的最大组织与背景比值时进一步得到改善。结论:冠状动脉18f -氟化物活性是冠状血管中一种精确、可重复的测量方法。18f -氟化物的分析性能足以评估这种放射性示踪剂作为斑块易损性的无创成像生物标志物的预后效用。临床试验注册:网址:http://www.clinicaltrials.gov。唯一标识符:NCT02110303和NCT02278211。
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来源期刊
CiteScore
3.20
自引率
15.00%
发文量
12
审稿时长
>12 weeks
期刊介绍: The subject of the origin and early evolution of life is an inseparable part of the general discipline of Astrobiology. The journal Origins of Life and Evolution of Biospheres places special importance on the interconnection as well as the interdisciplinary nature of these fields, as is reflected in its subject coverage. While any scientific study which contributes to our understanding of the origins, evolution and distribution of life in the Universe is suitable for inclusion in the journal, some examples of important areas of interest are: prebiotic chemistry and the nature of Earth''s early environment, self-replicating and self-organizing systems, the theory of the RNA world and of other possible precursor systems, and the problem of the origin of the genetic code. Early evolution of life - as revealed by such techniques as the elucidation of biochemical pathways, molecular phylogeny, the study of Precambrian sediments and fossils and of major innovations in microbial evolution - forms a second focus. As a larger and more general context for these areas, Astrobiology refers to the origin and evolution of life in a cosmic setting, and includes interstellar chemistry, planetary atmospheres and habitable zones, the organic chemistry of comets, meteorites, asteroids and other small bodies, biological adaptation to extreme environments, life detection and related areas. Experimental papers, theoretical articles and authorative literature reviews are all appropriate forms for submission to the journal. In the coming years, Astrobiology will play an even greater role in defining the journal''s coverage and keeping Origins of Life and Evolution of Biospheres well-placed in this growing interdisciplinary field.
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