Marked variation in atherosclerotic plaque progression between the major epicardial coronary arteries

Author:

Bax A Maxim1,Lin Fay Y1,van Rosendael Alexander R2,Ma Xiaoyue3,Lu Yao3,van den Hoogen Inge J2,Gianni Umberto1,Tantawy Sara W1,Andreini Daniele4,Budoff Matthew J5ORCID,Cademartiri Filippo6ORCID,Chinnaiyan Kavitha7,Choi Jung Hyun8,Conte Edoardo4,de Araújo Gonçalves Pedro9,Gottlieb Ilan10,Hadamitzky Martin11,Leipsic Jonathon A12,Maffei Erica13,Pontone Gianluca4ORCID,Stone Gregg14,Shin Sanghoon15,Kim Yong-Jin16,Lee Byoung Kwon17,Chun Eun Ju18,Sung Ji Min1920,Lee Sang-Eun1520,Berman Daniel S21,Narula Jagat22,Chang Hyuk-Jae1920ORCID,Shaw Leslee J1ORCID

Affiliation:

1. Department of Radiology, Dalio Institute of Cardiovascular Imaging, NewYork-Presbyterian Hospital and Weill Cornell Medicine , 413 East 69th Street, Suite 108, New York, NY 10021 , USA

2. Department of Cardiology, Leiden University Medical Center , Leiden , The Netherlands

3. Department of Healthcare Policy and Research, NewYork-Presbyterian Hospital and the Weill Cornell Medical College , New York, NY , USA

4. Department of Perioperative Cardiology and Cardiovascular Imaging, Centro Cardiologico Monzino IRCCS , Milan , Italy

5. Department of Medicine, Los Angeles Biomedical Research Institute , Torrance, CA , USA

6. Department of Radiology, Fondazione Monasterio-CNR (FTGM) , Pisa , Italy

7. Department of Cardiology, William Beaumont Hospital , Royal Oak, MI , USA

8. Division of Cardiology, Department of Internal Medicine, Pusan University Hospital , Busan , South Korea

9. Departmento of Cardiology, UNICA, Unit of Cardiovascular Imaging, Hospital da Luz , Lisboa , Portugal

10. Department of Radiology, Casa de Saude São Jose , Rio de Janeiro , Brazil

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

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

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

14. The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai , New York, NY , USA

15. Division of Cardiology, Department of Internal Medicine, Ewha Womans University Seoul Hospital , Seoul , Korea

16. Department of Internal Medicine, Seoul National University College of Medicine, Cardiovascular Center, Seoul National University Hospital , Seoul , South Korea

17. Division of Cardiology, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine , Seoul , Korea

18. Department of Radiology, Seoul National University Bundang Hospital , Sungnam , South Korea

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

20. Yonsei-Cedars-Sinai Integrative Cardiovascular Imaging Research Center, Yonsei University College of Medicine, Yonsei University Health System , Seoul , South Korea

21. Department of Imaging and Medicine, Cedars Sinai Medical Center , Los Angeles, CA , USA

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

Abstract

Abstract Aims Atherosclerosis develops progressively and worsens over time, yet event risk patterns vary in the left circumflex (LCx), right coronary artery (RCA) and left anterior descending (LAD). The aim of this analysis was to examine varying progressive disease alterations between the three major coronary arteries. Methods and results Patients were included from a prospective, international registry of consecutive patients who underwent serial CCTA at a median interval of 3.3 years. Annual progression of quantitative total and compositional plaque volume were compared between the three coronary arteries (LCx, LAD, and RCA). Other analyses compared stenosis ≥50% and new high-risk plaque (HRP; ≥2 of the following: spotty calcification, positive remodelling, napkin-ring sign, and low-attenuation plaque) on follow-up. Generalized estimating equations and marginal Cox regression models were used to compare progression, with covariate adjustment by the baseline atherosclerotic cardiovascular disease risk score, statin use, and plaque burden. Quantitative plaque measurements were calculated in 1344 patients (age 60 ± 9 years, 57% men). Plaque progression occurred less often in the LCx (41.0%) as compared to the RCA (52.7%) and LAD (77.4%, P < 0.001). Odds for annual plaque burden increase ≥population mean were 1.98- and 1.43-fold as high in the LAD (P < 0.001) and RCA (P < 0.001) as compared to the LCx. Similarly, the LAD was associated with a 2.45 higher risk of progression to obstructive CAD (P < 0.001), as compared to the LCx; with no differences between the RCA and LCx (P = 0.13). New HRP lesions formed least often in the LCx (3.4%), followed by the RCA (8.1%) and most often in the LAD (10.1%; P < 0.001). Conclusions Our findings reveal novel insights into varied patterns of atherosclerotic plaque progression within the LCx as compared to the other epicardial coronary arteries. These varied patterns reflect differing stages in the disease process or differing pathogenic milieu across the coronary arteries.

Funder

Ministry of Science and ICT

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,General Medicine

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