Left ventricular hypertrophy, aortic wall thickness, and lifetime predicted risk of cardiovascular disease:the Dallas Heart Study
Related Experiment Video
Updated: Jun 12, 2026

Ascending Aortic Constriction in Rats for Creation of Pressure Overload Cardiac Hypertrophy Model
Published on: June 29, 2014
Sachin Gupta1, Jarett D Berry, Colby R Ayers
1Division of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Insights
Individuals with low short-term coronary heart disease risk but high lifetime cardiovascular disease (CVD) risk show increased left ventricular (LV) hypertrophy and aortic wall thickness (AWT). This highlights subclinical abnormalities beyond coronary artery calcium in predicting future CVD risk.
Area of Science:
- Cardiology
- Cardiovascular Disease Research
- Preventive Cardiology
Background:
- Lifetime risk prediction stratifies individuals under 50 into low/high cardiovascular disease (CVD) risk groups.
- High lifetime CVD risk is linked to subclinical atherosclerosis, but coronary artery calcium is not always detectable.
- Alternative subclinical markers may indicate increased CVD risk in younger adults.
Purpose of the Study:
- To investigate if individuals with low short-term coronary heart disease (CHD) risk but high lifetime CVD risk exhibit greater left ventricular (LV) hypertrophy and aortic wall thickness (AWT).
- To compare subclinical cardiovascular abnormalities between low short-term/high lifetime risk and low short-term/low lifetime risk groups.
Main Methods:
- Cardiac magnetic resonance imaging was used to assess 1,804 Dallas Heart Study participants aged 30-50 years.
- Participants were stratified into low/low lifetime risk, low short-term/high lifetime risk, and high short-term risk groups.
- LV hypertrophy and AWT were compared between low short-term risk groups with differing lifetime risks.
Main Results:
- Individuals with low short-term/high lifetime CVD risk had significantly increased LV mass compared to those with low short-term/low lifetime risk (p < 0.001).
- LV concentricity, wall thickness, and AWT were also significantly greater in the high lifetime risk group (p < 0.001).
- These findings were consistent even in participants without detectable coronary artery calcium.
Conclusions:
- A high lifetime predicted CVD risk is associated with concentric LV hypertrophy and increased AWT in individuals aged 30-50 with low short-term risk.
- These subclinical changes indicate a higher cardiovascular risk profile.
- Lifetime risk assessment identifies individuals needing closer monitoring for CVD, even with low immediate risk.
Objectives:
To examine whether individuals with low short-term risk of coronary heart disease but high lifetime predicted risk of cardiovascular disease (CVD) have greater prevalence of left ventricular (LV) hypertrophy and increased aortic wall thickness (AWT) than those with low short-term and low lifetime risk.
Background:
Lifetime risk prediction can be used for stratifying individuals younger than 50 years of age into 2 groups: low short-term/high lifetime and low short-term/low lifetime predicted risk of CVD. Individuals with low short-term/high lifetime risk have a greater burden of subclinical atherosclerosis as measured by coronary artery calcium and carotid intima-media thickness. However, >75% of individuals with low short-term/high lifetime risk do not have detectable coronary artery calcium, suggesting the presence of alternative subclinical abnormalities.
Methods:
We stratified 1,804 Dallas Heart Study subjects between the ages of 30 and 50 years who had cardiac magnetic resonance into 3 groups: low short-term (<10% 10-year risk of coronary heart disease)/low lifetime predicted risk (<39% lifetime risk of CVD), low short-term (<10%)/high lifetime risk (> or =39%), and high short-term risk (> or =10%, prevalent diabetes, or previous stroke, or myocardial infarction). In those with low short-term risk, we compared measures of LV hypertrophy and AWT between those with low versus high lifetime risk.
Results:
Subjects with low short-term/high lifetime risk compared with those with low short-term/low lifetime risk had increased LV mass (men: 95 +/- 17 g/m(2) vs. 90 +/- 12 g/m(2) and women: 75 +/- 14 g/m(2) vs. 71 +/- 10 g/m(2), respectively; p < 0.001 for both). LV concentricity (mass/volume), wall thickness, and AWT were also significantly greater in those with high lifetime risk in this comparison (p < 0.001 for all), but LV end-diastolic volume was not (p > 0.3). These associations persisted among participants without detectable coronary artery calcium.
Conclusions:
Among individuals 30 to 50 years of age with low short-term risk, a high lifetime predicted risk of CVD is associated with concentric LV hypertrophy and increased AWT.
Related Concept Videos
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Heart Failure II: Pathophysiology
Aortic Regurgitation II: Clinical Features and Diagnostic Tests
Coronary Artery Disease I: Introduction
Atherosclerosis II: Clinical Manifestations and Diagnostic Tests
Aortic Regurgitation III: Medical Management
