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Updated: May 15, 2026

Pulse Wave Velocity Testing in the Baltimore Longitudinal Study of Aging
Published on: February 7, 2014
Aortic pulse wave velocity measurement in systemic sclerosis patients
M Colaci1, D Giuggioli, A Manfredi
1Rheumatology Unit, Centre of Lung Rare Diseases, MaRP,University of Modena and Reggio Emilia, Modena, Italy. michelecolaci@virgilio.it
Insights
Systemic sclerosis patients show significantly increased aortic pulse wave velocity (aPWV), indicating greater arterial stiffness. This finding suggests more widespread vascular damage in specific SSc subsets.
Area of Science:
- Cardiovascular Medicine
- Rheumatology
- Vascular Biology
Background:
- Systemic sclerosis (SSc) involves endothelial dysfunction and microangiopathy, with potential macrovascular implications.
- Aortic pulse wave velocity (aPWV) is a key indicator of arterial stiffness and cardiovascular event prognosis.
- Non-invasive measurement of aPWV offers a practical tool for assessing vascular health.
Purpose of the Study:
- To evaluate alterations in aortic pulse wave velocity (aPWV) in patients with Systemic Sclerosis (SSc).
- To correlate aPWV findings with cardiopulmonary involvement in SSc patients.
- To identify potential subsets of SSc patients with increased vascular damage.
Main Methods:
- Aortic pulse wave velocity (aPWV) was measured in 35 female SSc patients and 26 age- and sex-matched healthy controls.
- Echocardiography was used to assess cardiac structure and pulmonary arterial systolic pressure (PAPs).
- Clinical parameters including the six-minute walking test and disease characteristics were analyzed.
Main Results:
- SSc patients exhibited significantly higher aPWV compared to controls (9.4 ± 3.2 m/s vs 7.3 ± 1 m/s, P=0.002).
- Increased aPWV (>9 m/s) was found in 40% of SSc patients versus 4% of controls (P=0.0009).
- SSc patients showed increased right atrial/ventricular dilatation, elevated PAPs, and reduced six-minute walking test distance, particularly those >50 years old, with limited cutaneous SSc, longer disease duration, or ACA positivity.
Conclusions:
- A significantly higher prevalence of elevated aPWV was observed in SSc patients, indicating increased arterial stiffness.
- These findings suggest more pronounced and diffuse vascular damage in specific SSc subsets, such as ACA-positive individuals with limited cutaneous scleroderma and longer disease duration.
- aPWV may serve as a valuable non-invasive marker for assessing macrovascular involvement in Systemic Sclerosis.
Background:
Systemic sclerosis (SSc) is characterized by endothelial dysfunction and widespread microangiopathy. However, a macrovascular damage could be also associated. Aortic pulse wave velocity (aPWV) is known to be a reliable indicator of arterial stiffness and a useful prognostic predictor of cardiovascular events. Moreover, aPWV may be easily measured by non-invasive, user-friendly tool. Aim of our study was to evaluate aPWV alterations in a series of SSc patients.
Methods:
The aPWV was evaluated in 35 consecutive female SSc patients and 26 sex- and age-matched healthy controls. aPWV alterations were correlated with cardiopulmonary involvement.
Results:
A significant increase of aPWV was observed in SSc patients compared to controls (9.4 ± 3.2 m/s vs 7.3 ± 1 m/s; P = 0.002). In particular, 14/35 (40%) SSc patients and only 1/26 (4%) controls (P=0.0009) showed increased aPWV (>9 m/s cut-off value). Moreover, echocardiography evaluation showed an increased prevalence of right atrial and ventricular dilatation (atrial volume: 23.6 ± 6.2 mL vs 20.3 ± 4.3 mL, P=0.026; ventricular diameter 19.5 ± 4.9 mm vs 15.9 ± 1.6 mm; P=0.001) associated to higher values of pulmonary arterial systolic pressure (PAPs) in SSc patients (31.5 ± 10.4 mmHg vs 21.6 ± 2.9 mmHg; P<0.0001; 40% of SSc patients showed an abnormal PAPs). Clinically, SSc patients presented a reduction of six-minute walking test (413 ± 96 m vs 491 ± 49 m; P=0.001), not correlated with pulmonary function tests. Increased aPWV values were evidenced only in SSc patients >50 years old. Furthermore, altered aPWV was more frequently associated with limited cutaneous pattern, longer disease duration (≥ 5 years), and/or presence of anticentromere antibody (ACA).
Conclusions:
A significantly higher prevalence of abnormally increased aPWV was evidenced in SSc patients compared to healthy controls. The possibility of more pronounced and diffuse vascular damage in a particular SSc subset (ACA-positive subjects with limited cutaneous scleroderma and longer disease duration) might be raised.
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