Why the study?
Coronary artery disease progresses alongside myocardial disease, but data evaluating the association between coronary artery calcium and echocardiographic variables were lacking.
Does higher coronary artery calcium (CAC) score correlate with worse echocardiographic indices of cardiac remodeling in adults without overt clinical CHD?
Cross-Sectional (n=2,650)
Does higher coronary artery calcium (CAC) score correlate with worse echocardiographic indices of cardiac remodeling in adults without overt clinical CHD?
Subclinical atherosclerosis, as measured by coronary artery calcium, is modestly associated with left ventricular and aortic root remodeling even in individuals without overt cardiovascular disease.
Answers are grounded in this paper and cite their sources.
CAC-LVMi association in observational data should not change practice; leaves open whether atherosclerosis contributes to remodeling.
BACKGROUND: It is well established that coronary artery disease progresses along with myocardial disease. However, data on the association between coronary artery calcium (CAC) and echocardiographic variables are lacking. METHODS AND RESULTS: Among 2,650 Framingham Study participants (mean age 51 yrs, 48% women; 40% with CAC>0), we related CT-based CAC score to left ventricular (LV) mass index (LVMi), LV ejection fraction (LVEF), E/e', global longitudinal strain (GLS), left atrial emptying fraction (LAEF), and aortic root diameter (AoR), using multivariable-adjusted generalized linear models. CAC score (independent variable) was used as log-transformed continuous [ln(CAC+1)] and as a categorical (0, 1-100, and ≥101) variable. Adjusting for standard risk factors, higher CAC score was associated with higher LVMi and AoR (βLVMI per 1-SD increase 0.012, βAoR 0.008; P<0.05, for both). Participants with 1≤CAC≤100 and those with CAC≥101 had higher AoR (βAoR 0.013 and 0.020, respectively, P = 0.01) than those with CAC = 0. CAC score was not significantly associated with LVEF, E/e', GLS or LAEF. Age modified the association of CAC score with AoR; higher CAC scores were associated with larger AoR more strongly in older (>58 years; βAoR0.0042;P<0.007) than in younger (≤58 years) participants (βAoR0.0027;P<0.03). CONCLUSIONS: We observed that subclinical atherosclerosis was associated with ventricular and aortic remodeling. The prognostic significance of these associations warrants evaluation in additional mechanistic studies.
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Castro‐Diehl et al. (2020) conducted a cross-sectional in Subclinical atherosclerosis (n=2,650). Coronary artery calcium (CAC) vs. CAC = 0 was evaluated on Left ventricular mass index (LVMi) (β 0.012, p=0.048).
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