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Updated: Jan 11, 2026

Pulse Wave Velocity Testing in the Baltimore Longitudinal Study of Aging
Published on: February 7, 2014
Prediction of cardiovascular events by algorithm- and formula-based pulse wave velocity
Louis-Charles Desbiens1, Simon Veillette1, Catherine Fortier2,3
1Department of Medicine, Université de Montréal, Montreal.
Insights
Algorithm-based pulse wave velocity (PWV) estimation significantly enhances cardiovascular risk prediction beyond current tools. Formula-based estimations may lack generalizability, highlighting the value of algorithmic approaches for arterial stiffness assessment.
Area of Science:
- Cardiology
- Vascular Biology
- Preventive Medicine
Background:
- Carotid-femoral pulse wave velocity (PWV) is a key indicator of arterial stiffness and a cardiovascular disease risk factor.
- Current methods for measuring PWV are time-consuming, prompting the development of estimation techniques.
- The clinical utility of estimated PWV (ePWV) in improving cardiovascular risk prediction beyond existing tools remains uncertain.
Purpose of the Study:
- To evaluate the ability of two ePWV methods—formula-based (ePWV f) and algorithm-based (ePWV algo)—to predict major adverse cardiovascular events (MACE).
- To determine if ePWV improves cardiovascular risk prediction when added to established risk scores like ASCVD and SCORE-2.
Main Methods:
- Utilized data from the population-based CARTaGENE cohort (40-69 years).
- Calculated ePWV using published formulas (ePWV f) and algorithmic transformation (ePWV algo).
- Assessed 10-year MACE risk using ASCVD and SCORE-2 equations, then employed Cox models to analyze associations between ePWV and MACE, adjusting for risk scores.
Main Results:
- Of 17,548 participants, 2263 (12.9%) experienced MACE.
- ePWV algo was significantly associated with MACE after adjustment for ASCVD (HR=1.16) and SCORE-2 (HR=1.07).
- ePWV f did not show significant association with MACE after adjustment for either risk score in the overall cohort.
Conclusions:
- Algorithm-based ePWV enhances cardiovascular risk prediction beyond conventional risk equations.
- The predictive performance of formula-based ePWV may be limited to specific populations from which it was derived.
- Algorithmic ePWV offers a more generalizable and valuable tool for cardiovascular risk assessment.
Background:
Carotid-femoral pulse wave velocity (PWV), a marker of arterial stiffness, is a recognized cardiovascular disease risk factor. As measuring PWV is time-consuming, reliable estimation methods have been developed, but their ability to inform cardiovascular risk prediction beyond what is achievable with current clinical risk tools is uncertain.
Methods:
This study includes participants aged between 40 and 69 years from the population-based CARTaGENE cohort. PWV estimations (ePWV) were obtained using published formulas (ePWV f ) or algorithmic transformation of pulse waveforms (ePWV algo ) and 10-year cardiovascular risk for each participant was computed using the ASCVD and the SCORE-2 risk equations. Participants were followed during 10 years for major adverse cardiovascular events occurrence (MACE: cardiovascular death, myocardial infarction, stroke). Associations of ePWV f and ePWV algo with MACE were obtained using Cox models adjusted for ASCVD or SCORE-2 in the overall population and in a subpopulation representative of the ePWV f derivation cohort.
Results:
Of 17 548 eligible participants, 2263 (12.9%) experienced a MACE during follow-up. Both ePWVf and ePWV algo were associated with MACE in unadjusted analyses, but only ePWV algo remained significant after adjustments for ASCVD [hazard ratio (HR) = 1.16 [1.09-1.22]] and SCORE-2 (HR = 1.07 [1.00-1.13]). In contrast, ePWV f was not associated with MACE after adjustment for either risk score, and only after adjustment with ASCVD when it was tested in the subpopulation representative of its derivation cohort.
Conclusions:
Algorithm-based PWV improved cardiovascular risk prediction beyond what is achievable from recognized risk equations, whereas the predictive ability of ePWV f may not be generalizable outside of its reference population.
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