Relationship Between Coronary Artery Calcium and Atherosclerosis Progression Among Patients With Suspected Coronary Artery Disease

被引:37
作者
Hollenberg, Emma J. [1 ,2 ,3 ]
Lin, Fay [1 ,2 ]
Blaha, Michael J. [4 ,27 ]
Budoff, Matthew J. [5 ]
van den Hoogen, Inge J. [1 ,2 ,6 ]
Gianni, Umberto [1 ,2 ]
Lu, Yao [7 ,8 ]
Bax, A. Maxim [1 ,2 ]
van Rosendael, Alexander R. [1 ,2 ,6 ]
Tantawy, Sara W. [1 ,2 ]
Andreini, Daniele [9 ]
Cademartiri, Filippo [10 ]
Chinnaiyan, Kavitha [11 ]
Choi, Jung Hyun [12 ]
Conte, Edoardo [9 ]
Goncalves, Pedro de Araujo [13 ]
Hadamitzky, Martin [14 ]
Maffei, Erica [15 ]
Pontone, Gianluca [9 ]
Shin, Sanghoon [16 ]
Kim, Yong-Jin [17 ]
Lee, Byoung Kwon [18 ]
Chun, Eun Ju [19 ]
Sung, Ji Min [20 ]
Gimelli, Alessia [21 ]
Lee, Sang-Eun [22 ]
Bax, Jeroen J. [6 ]
Berman, Daniel S. [23 ]
Sellers, Stephanie L. [24 ]
Leipsic, Jonathon A. [24 ]
Blankstein, Ron [25 ]
Narula, Jagat [26 ]
Chang, Hyuk-Jae [20 ]
Shaw, Leslee J. [26 ]
机构
[1] New York Presbyterian Hosp, Dalio Inst Cardiovasc Imaging, New York, NY USA
[2] Weill Cornell Med, New York, NY USA
[3] Emory Univ, Sch Med, Atlanta, GA USA
[4] Johns Hopkins Univ, Ciccarone Ctr Prevent Cardiovasc Dis, Sch Med, Baltimore, MD USA
[5] Harbor UCLA Med Ctr, Dept Med, Lundquist Inst, Torrance, CA 90509 USA
[6] Leiden Univ, Med Ctr, Dept Cardiol, Leiden, Netherlands
[7] New York Presbyterian Hosp, Dept Healthcare Policy & Res, New York, NY USA
[8] Weill Cornell Med Coll, New York, NY USA
[9] IRCCS, Ctr Cardiol Monzino, Milan, Italy
[10] SDN IRCCS, Cardiovasc Imaging Ctr, Naples, Italy
[11] William Beaumont Hosp, Dept Cardiol, Royal Oak, MI 48072 USA
[12] Pusan Univ Hosp, Busan, South Korea
[13] Nova Med Sch, Hosp Luz, Unit Cardiovasc Imaging, UNICA, Lisbon, Portugal
[14] German Heart Ctr, Dept Radiol & Nucl Med, Munich, Germany
[15] Area Vasta 1 ASUR Marche, Dept Radiol, Urbino, Italy
[16] Ewha Womans Univ, Seoul Hosp, Dept Internal Med, Div Cardiol, Seoul, South Korea
[17] Seoul Natl Univ, Seoul Natl Univ Hosp, Cardiovasc Ctr, Dept Internal Med,Coll Med, Seoul, South Korea
[18] Yonsei Univ, Gangnam Severance Hosp, Coll Med, Seoul, South Korea
[19] Seoul Natl Univ, Bundang Hosp, Sungnam, South Korea
[20] Yonsei Univ, Yonsei Univ Hlth Syst, Severance Cardiovasc Hosp, Div Cardiol,Coll Med, Seoul, South Korea
[21] Fdn Toscana Gabriele Monasterio, Dept Imaging, Pisa, Italy
[22] Yonsei Univ, Yonsei Univ Hlth Syst, Yonsei Cedars Sinai Integrat Cardiovasc Imaging R, Coll Med, Seoul, South Korea
[23] Cedars Sinai Med Ctr, Dept Imaging & Med, Los Angeles, CA 90048 USA
[24] Univ British Columbia, Dept Med & Radiol, Vancouver, BC, Canada
[25] Harvard Med Sch, Brigham & Womens Hosp, Div Cardiol, Boston, MA 02115 USA
[26] Icahn Sch Med Mt Sinai, Mt Sinai Heart, Zena & Michael A Wiener Cardiovasc Inst, New York, NY 10128 USA
[27] Marie Josee & Henry R Kravis Ctr Cardiovasc Hlth, New York, NY USA
基金
新加坡国家研究基金会;
关键词
atherosclerotic plaque; coronary artery calcium; coronary computed tomographic angiography; plaque progression; CARDIOVASCULAR COMPUTED-TOMOGRAPHY; NORTH-AMERICAN SOCIETY; ANGIOGRAPHY; QUANTIFICATION; SCORE;
D O I
10.1016/j.jcmg.2021.12.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Among symptomatic patients, it remains unclear whether a coronary artery calcium (CAC) score alone is sufficient or misses a sizeable burden and progressive risk associated with obstructive and nonobstructive atherosclerotic plaque. OBJECTIVES Among patients with low to high CAC scores, our aims were to quantify co-occurring obstructive and nonobstructive noncalcified plaque and serial progression of atherosclerotic plaque volume. METHODS A total of 698 symptomatic patients with suspected coronary artery disease (CAD) underwent serial coronary computed tomographic angiography (CTA) performed 3.5 to 4.0 years apart. Atherosclerotic plaque was quantified, including by compositional subgroups. Obstructive CAD was defined as >= 50% stenosis. Multivariate linear regression models were used to measure atherosclerotic plaque progression by CAC scores. Cox proportional hazard models estimated CAD event risk (median of 10.7 years of follow-up). RESULTS Across baseline CAC scores from 0 to >= 400, total plaque volume ranged from 30.4 to 522.4 mm(3) (P < 0.001) and the prevalence of obstructive CAD increased from 1.4% to 49.1% (P < 0.001). Of those with a 0 CAC score, 97.9% of total plaque was noncalcified. Among patients with baseline CAC <100, nonobstructive CAD was prevalent (40% and 89% in CAC scores of 0 and 1-99), with plaque largely being noncalcified. On the follow-up coronary CTA, volumetric plaque growth (P < 0.001) and the development of new or worsening stenosis (P < 0.001) occurred more among patients with baseline CAC >= 100. Progression varied compositionally by baseline CAC scores. Patients with no CAC had disproportionate growth in noncalcified plaque, and for every 1 mm(3) increase in calcified plaque, there was a 5.5 mm(3) increase in noncalcified plaque volume. By comparison, patients with CAC scores of >= 400 exhibited disproportionate growth in calcified plaque with a volumetric increase 15.7-fold that of noncalcified plaque. There was a graded increase in CAD event risk by the CAC with rates from 3.3% for no CAC to 21.9% for CAC >= 400 (P < 0.001). CONCLUSIONS CAC imperfectly characterizes atherosclerotic disease burden, but its subgroups exhibit pathogenic patterns of early to advanced disease progression and stratify long-term prognostic risk. (C) 2022 by the American College of Cardiology Foundation.
引用
收藏
页码:1063 / 1074
页数:12
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