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Relationship between epicardial adipose tissue and coronary atherosclerosis by CCTA in young adults (18-45).
Filtz, Annalisa; Lorenzatti, Daniel; Scotti, Andrea; Piña, Pamela; Fernandez-Hazim, Carol; Huang, Dou; Ippolito, Paul; Skendelas, John P; Kuno, Toshiki; Rodriguez, Carlos J; Schenone, Aldo L; Latib, Azeem; Lavie, Carl J; Shaw, Leslee J; Blankstein, Ron; Shapiro, Michael D; Garcia, Mario J; Berman, Daniel S; Dey, Damini; Virani, Salim S; Slipczuk, Leandro.
Affiliation
  • Filtz A; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Lorenzatti D; IRCCS Ospedale Ca' Granda Maggiore Policlinico, Università degli Studi di Milano. Milan, Italy.
  • Scotti A; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Piña P; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Fernandez-Hazim C; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Huang D; Department of Cardiology, CEDIMAT. Santo Domingo, Dominican Republic.
  • Ippolito P; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Skendelas JP; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Kuno T; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Rodriguez CJ; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Schenone AL; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Latib A; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Lavie CJ; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Shaw LJ; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Blankstein R; John Ochsner Heart and Vascular Institute, Ochsner Clinic Foundation, New Orleans, LA, USA.
  • Shapiro MD; Departments of Medicine (Cardiology) and Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Garcia MJ; Departments of Medicine (Cardiovascular Division) and Radiology, Brigham and Women's Hospital. Boston, MA, USA.
  • Berman DS; Center for Prevention of Cardiovascular Disease, Section on Cardiovascular Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
  • Dey D; Cardiology Division, Montefiore Medical Center/Albert Einstein College of Medicine. Bronx, NY, USA.
  • Virani SS; Department of Imaging, Medicine, and Biomedical Sciences, Cedars-Sinai Medical Center. Los Angeles, CA, USA.
  • Slipczuk L; Department of Imaging, Medicine, and Biomedical Sciences, Cedars-Sinai Medical Center. Los Angeles, CA, USA.
Am J Prev Cardiol ; 19: 100711, 2024 Sep.
Article in En | MEDLINE | ID: mdl-39157644
ABSTRACT

Objective:

Epicardial adipose tissue (EAT) is implicated in the pathogenesis and progression of coronary artery disease (CAD). Limited data exists on the interplay between EAT and atherosclerosis in young individuals. Our study aims to explore the relationship between EAT and CAD in a young cohort.

Methods:

All young (18-45 years) patients without prior CAD, referred for coronary computed tomography angiography (CCTA) from 2016 to 2022 were included. EAT volume and coronary artery calcium (CAC) were calculated from dedicated non-contrast scans. Coronary plaque presence, extent, and volume were quantified from CCTA. Multivariable logistic regression models for the presence of CAD, defined as any coronary atherosclerosis, were performed.

Results:

Overall, 712 patients (39±4.8 years, 54 % female) with 45 % Hispanic, and 21 % non-Hispanic Black were included. Patients with CAD had higher EAT volume than those without (80.80 mL ± 36.00 vs 55.16 mL ± 27.92; P < 0.001). In those with CAC=0, higher EAT was associated with the presence of CAD compared to lower EAT volume (P < 0.001). An EAT volume >76 mL was associated with higher CAC (P < 0.001), segment involvement score (P < 0.001), and quantitative total, non-calcified, and low-attenuation plaque volumes (P < 0.002). At multivariable analysis, EAT volume (per 10 mL, OR 1.21; 95 %CI 1.12-1.30; P < 0.0001) was independently associated with the presence of CAD.

Conclusion:

In a diverse cohort of young adults without history of CAD and undergoing a clinically indicated CCTA, EAT volume was independently associated with the presence of CAD. Our findings highlight EAT potential as a novel marker for CAD risk-assessment and a potential therapeutic target in young patients.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Am J Prev Cardiol Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Am J Prev Cardiol Year: 2024 Document type: Article Affiliation country: Country of publication: