Association of Cardiovascular Disease Risk Factor Burden With Progression of Coronary Atherosclerosis Assessed by Serial Coronary Computed Tomographic Angiography.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 07 2020
Historique:
entrez: 25 7 2020
pubmed: 25 7 2020
medline: 22 12 2020
Statut: epublish

Résumé

Several studies have reported that the progression of coronary atherosclerosis, as measured by serial coronary computed tomographic (CT) angiography, is associated with the risk of future cardiovascular events. However, the cumulative consequences of multiple risk factors for plaque progression and the development of adverse plaque characteristics have not been well characterized. To examine the association of cardiovascular risk factor burden, as assessed by atherosclerotic cardiovascular disease (ASCVD) risk score, with the progression of coronary atherosclerosis and the development of adverse plaque characteristics. This cohort study is a subgroup analysis of participant data from the prospective observational Progression of Atherosclerotic Plaque Determined by Computed Tomographic Angiography Imaging (PARADIGM) study, which evaluated the association between serial coronary CT angiography findings and clinical presentation. The PARADIGM international multicenter registry, which includes 13 centers in 7 countries (Brazil, Canada, Germany, Italy, Portugal, South Korea, and the US), was used to identify 1005 adult patients without known coronary artery disease who underwent serial coronary CT angiography scans (median interscan interval, 3.3 years; interquartile range [IQR], 2.6-4.8 years) between December 24, 2003, and December 16, 2015. Based on the 10-year ASCVD risk score, the cardiovascular risk factor burden was classified as low (<7.5%), intermediate (7.5%-20.0%), or high (>20.0%). Data were analyzed from February 8, 2019, to April 17, 2020. Association of baseline ASCVD risk burden with plaque progression. Noncalcified plaque, calcified plaque, and total plaque volumes (mm3) were measured. Noncalcified plaque was subclassified using predefined Hounsfield unit thresholds for fibrous, fibrofatty, and low-attenuation plaque. The percent atheroma volume (PAV) was defined as plaque volume divided by vessel volume. Adverse plaque characteristics were defined as the presence of positive remodeling, low-attenuation plaque, or spotty calcification. In total, 1005 patients (mean [SD] age, 60 [8] years; 575 men [57.2%]) were included in the analysis. Of those, 463 patients (46.1%) had a low 10-year ASCVD risk score (low-risk group), 373 patients (37.1%) had an intermediate ASCVD risk score (intermediate-risk group), and 169 patients (16.8%) had a high ASCVD risk score (high-risk group). The annualized progression rate of PAV for total plaque, calcified plaque, and noncalcified plaque was associated with increasing ASCVD risk (r = 0.26 for total plaque, r = 0.23 for calcified plaque, and r = 0.11 for noncalcified plaque; P < .001). The annualized PAV progression of total plaque, calcified plaque, and noncalcified plaque was significantly greater in the high-risk group compared with the low-risk and intermediate-risk groups (for total plaque, 0.99% vs 0.45% and 0.58%, respectively; P < .001; for calcified plaque, 0.61% vs 0.23% and 0.36%; P < .001; and for noncalcified plaque, 0.38%vs 0.22% and 0.23%; P = .01). When further subclassified by noncalcified plaque type, the annualized PAV progression of fibrofatty and low-attenuation plaque was greater in the high-risk group (0.09% and 0.02%, respectively) compared with the low- to intermediate-risk group (n = 836; 0.02% [P = .02] and 0.001% [P = .008], respectively). The interval development of adverse plaque characteristics was greater in the high-risk group compared with the low-risk and intermediate-risk groups (for new positive remodeling, 73 patients [43.2%] vs 151 patients [32.6%] and 133 patients [35.7%], respectively; P = .02; for new low-attenuation plaque, 26 patients [15.4%] vs 44 patients [9.5%] and 35 patients [9.4%]; P = .02; and for new spotty calcification, 37 patients [21.9%] vs 52 patients [11.2%] and 54 patients [14.5%]; P = .002). The progression of noncalcified plaque subclasses and the interval development of adverse plaque characteristics did not significantly differ between the low-risk and intermediate-risk groups. Progression of coronary atherosclerosis occurred across all ASCVD risk groups and was associated with an increase in 10-year ASCVD risk. The progression of fibrofatty and low-attenuation plaques and the development of adverse plaque characteristics was greater in patients with a high risk of ASCVD.

Identifiants

pubmed: 32706382
pii: 2768616
doi: 10.1001/jamanetworkopen.2020.11444
pmc: PMC7382001
doi:

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2011444

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Auteurs

Donghee Han (D)

Department of Imaging and Medicine, Cedars-Sinai Medical Center, Los Angeles, California.
Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Yonsei University Health System, Seoul, South Korea.

Daniel S Berman (DS)

Department of Imaging and Medicine, Cedars-Sinai Medical Center, Los Angeles, California.

Robert J H Miller (RJH)

Department of Imaging and Medicine, Cedars-Sinai Medical Center, Los Angeles, California.
Department of Cardiac Sciences, University of Calgary, Calgary, Alberta, Canada.

Daniele Andreini (D)

Centro Cardiologico Monzino, Institute for Research, Hospitalization and Healthcare (IRCCS), Milan, Italy.

Matthew J Budoff (MJ)

Department of Medicine, Los Angeles Biomedical Research Institute, Torrance, California.

Filippo Cademartiri (F)

Cardiovascular Imaging Center, SDN Institute, Institute for Research, Hospitalization and Healthcare (IRCCS), Naples, Italy.

Kavitha Chinnaiyan (K)

Department of Cardiology, William Beaumont Hospital, Royal Oak, Michigan.

Jung Hyun Choi (JH)

Pusan National University Hospital, Busan, South Korea.

Edoardo Conte (E)

Centro Cardiologico Monzino, Institute for Research, Hospitalization and Healthcare (IRCCS), Milan, Italy.

Hugo Marques (H)

UNICA, Unit of Cardiovascular Imaging, Hospital da Luz, Lisbon, Portugal.

Pedro de Araújo Gonçalves (P)

UNICA, Unit of Cardiovascular Imaging, Hospital da Luz, Lisbon, Portugal.

Ilan Gottlieb (I)

Department of Radiology, Casa de Saúde São José, Rio de Janeiro, Brazil.

Martin Hadamitzky (M)

Department of Radiology and Nuclear Medicine, German Heart Center Munich, Munich, Germany.

Jonathon Leipsic (J)

Department of Medicine and Radiology, University of British Columbia, Vancouver, British Columbia, Canada.

Erica Maffei (E)

Department of Radiology, Area Vasta 1-ASUR Marche, Urbino, Italy.

Gianluca Pontone (G)

Centro Cardiologico Monzino, Institute for Research, Hospitalization and Healthcare (IRCCS), Milan, Italy.

Sangshoon Shin (S)

Ewha Womans University Seoul Hospital, Seoul, South Korea.

Yong-Jin Kim (YJ)

Seoul National University Hospital, Seoul, South Korea.

Byoung Kwon Lee (BK)

Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.

Eun Ju Chun (EJ)

Seoul National University Bundang Hospital, Sungnam, South Korea.

Ji Min Sung (JM)

Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Yonsei University Health System, Seoul, South Korea.

Sang-Eun Lee (SE)

Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Yonsei University Health System, Seoul, South Korea.

Renu Virmani (R)

Department of Pathology, CVPath Institute, Gaithersburg, Maryland.

Habib Samady (H)

Division of Cardiology, Emory University School of Medicine, Atlanta, Georgia.

Peter Stone (P)

Cardiovascular Division, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts.

Jagat Narula (J)

Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, Mount Sinai Heart, New York, New York.
Marie-Josée and Henry R. Kravis Center for Cardiovascular Health, New York, New York.

Jeroen J Bax (JJ)

Department of Cardiology, Leiden University Medical Center, Leiden, the Netherlands.

Leslee J Shaw (LJ)

Department of Radiology, New York-Presbyterian Hospital and Weill Cornell Medicine, New York, New York.

Fay Y Lin (FY)

Department of Radiology, New York-Presbyterian Hospital and Weill Cornell Medicine, New York, New York.

James K Min (JK)

Cleerly, Inc, New York, New York.

Hyuk-Jae Chang (HJ)

Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Yonsei University Health System, Seoul, South Korea.

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