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Updated: Jan 14, 2026

Pulse Wave Velocity Testing in the Baltimore Longitudinal Study of Aging
Published on: February 7, 2014
Relationship Between Framingham 10-Year Cardiovascular Disease Risk Score and Pulse Wave Amplitude Drop
Glenn M Stewart1, Benjamin K Tong1, Philip deChazal2
1Charles Perkins Centre, University of Sydney, Camperdown, NSW, Australia; Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Camperdown, NSW, Australia; Department of Respiratory and Sleep Medicine, Royal North Shore Hospital, St. Leonards, Camperdown, NSW, Australia.
Background:
Pulse oximetry-derived measures of autonomic vascular re-activity during sleep, quantified by pulse wave amplitude drop (PWAD) characteristics such as the PWAD index, have recently been proposed as a biomarker of cardiovascular disease (CVD) outcomes in patients with OSA.
Research Question:
Are PWAD characteristics associated with Framingham 10-year CVD risk score in a sleep clinic population?
Study Design And Methods:
This study examined PWAD characteristics in 725 individuals (38% female; median [interquartile range] age, 52 [39-63] years; BMI, 28.6 [24.9-33.2] kg/m2) who underwent diagnostic polysomnography and had sufficient clinical data to determine CVD status and calculate a Framingham 10-year CVD risk score. Individuals were categorized as either having established CVD (CVDESTABLISHED, n = 110) or a Framingham 10-year CVD risk score that was elevated (CVDELEVATED, n = 407) or low (CVDLOW, n = 208). Standard polysomnography variables and PWAD characteristics, including PWADINDEX (number of PWAD events that occurred during all sleep stages divided by total sleep time [events/h]) and PWADDURATION (average duration of PWAD events [seconds]), were compared between groups.
Results:
The PWADINDEX was lower (P < .01) in the CVDESTABLISHED (28.5 [13.2-45.2] events/h) and CVDELEVATED (38.7 [20.8-53.0] events/h) groups than in the CVDLOW group (47.7 [35.7-62.6] events/h). The PWADDURATION was longer (P < .01) in CVDESTABLISHED (10.4 [8.2-14.5] seconds) and CVDELEVATED (8.7 [7.6-10.1] seconds) groups than in CVDLOW group (8.0 [7.2-8.8] seconds). Similar group differences were observed during rapid-eye movement and non-rapid-eye movement sleep, and in patients with and without OSA. The magnitude difference in PWADINDEX and PWADDURATION remained similar after adjusting for age, sex, BMI, BP, total sleep time, apnea-hypopnea index, and oxygen desaturation index (adjusted PWADINDEX [95% CI] was 34.2 [29.9-38.7] in CVDESTABLISHED, 39.4 [37.1-41.6] in CVDELEVATED, and 46.6 [42.5-50.7] in CVDLOW; P < .01).
Interpretation:
These data indicate that PWAD characteristics may provide a complementary marker of CVD risk in sleep clinic populations with and without OSA. The pathophysiologic mechanisms linking nocturnal PWAD characteristics and CVD risk require further study.
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