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Published on: September 27, 2024
Subclinical Cardiovascular Disease and Changes in Self-Reported Mobility: Multi-Ethnic Study of Atherosclerosis
Susan A Everson-Rose1, Carlos F Mendes de Leon2, Nicholas S Roetker3
1Department of Medicine, University of Minnesota Medical School, Minneapolis.
Insights
Subclinical cardiovascular disease markers like intimal-medial thickening are linked to slower walking pace in older adults. However, these markers show limited impact on changes in walking speed over time.
Area of Science:
- Cardiology
- Gerontology
- Public Health
Background:
- Subclinical cardiovascular disease (CVD) is a precursor to clinical CVD.
- Markers include intimal-medial thickening, coronary artery calcification, and ankle-brachial index.
- Walking pace and time are indicators of physical function.
Purpose of the Study:
- To investigate the association between subclinical CVD markers and changes in self-reported walking over time.
- To determine if baseline CVD markers predict declines in walking pace and time.
Main Methods:
- Analysis of data from 6,490 Multi-Ethnic Study of Atherosclerosis participants (aged 45-84).
- Assessment of walking pace and time over 11 years.
- Linear generalized estimating equation models used to assess associations.
Main Results:
- Walking pace and time significantly decreased yearly over the 11-year follow-up.
- Greater intimal-medial thickening was associated with a faster decline in walking pace.
- Coronary artery calcification was linked to slower walking pace, but not consistently to its decline.
- Higher ankle-brachial index correlated with faster baseline walking pace but not changes in pace.
Conclusions:
- Subclinical CVD is associated with slower walking pace in middle-aged and older adults.
- Subclinical CVD markers have a limited effect on the rate of decline in walking over time.
Background:
We examined associations of three markers of subclinical cardiovascular disease (intimal-medial thickening, coronary artery calcification , and ankle-brachial index) with changes in self-reported walking over time.
Methods:
Data were from 6,490 Multi-Ethnic Study of Atherosclerosis participants (aged 45-84 years), free of clinical cardiovascular disease at baseline. Outcomes, assessed four times over 11 years, included self-reported walking pace (none to striding pace; score, 0-4) and total walking time (minutes/week). Linear generalized estimating equation models estimated associations of baseline intimal-medial thickening (z-scored), coronary artery calcification (Agatston units), and ankle-brachial index (ratio of ankle-to-arm systolic blood pressure) with walking pace and walking time modeled continuously in separate analyses.
Results:
Median follow-up was 9.2 years (maximum, 11.4). Walking pace (estimate, -0.042 points [95% CI; -0.048, -0.036], p < 0.0001) and walking time (estimate, -4.71 minutes [95% CI: -8.54, -0.88], p = 0.016) decreased yearly. Greater baseline intimal-medial thickening related to faster decline in walking pace in multivariable analyses: walking pace score decreased 0.004 points (95% CI: -0.008, -0.001) more per year for each 1-SD higher intimal-medial thickening z-score, equivalent to an additional 10% slower yearly walking. Greater coronary artery calcification was associated with slower walking but inconsistently related to decline in walking pace. Higher ankle-brachial index was associated with faster baseline walking pace (estimate, 0.043 points [95% CI: 0.027, 0.059] per 1-SD) but unrelated to changes in walking pace. Cardiovascular disease measures were unrelated to total walking time.
Conclusions:
Greater subclinical cardiovascular disease is associated with prevalent slower self-reported walking pace in middle-aged and older adults but has limited impact on changes in walking over time.
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