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Published on: December 2, 2014
Measurement of stiffness index by digital volume pulse analysis technique: clinical utility in cardiovascular disease
Ashan Gunarathne1, Jeetesh V Patel, Elizabeth A Hughes
1University Department of Medicine, City Hospital, Birmingham, UK.
Insights
Arterial stiffness index (SI) measured noninvasively using digital volume pulse (DVP) analysis effectively identifies cardiovascular disease (CVD) risk. This method aids in stratifying risk in apparently healthy individuals.
Area of Science:
- Cardiovascular Medicine
- Biomedical Engineering
- Public Health
Background:
- Arterial stiffness indices are established cardiovascular disease (CVD) markers.
- The diagnostic and prognostic value of stiffness index (SI) from digital volume pulse (DVP) analysis for CVD risk screening remains unclear.
Purpose of the Study:
- To evaluate the performance of SI derived from DVP analysis in discriminating increasing CVD risk.
- To assess the utility of SI in identifying individuals with established CVD risk factors.
Main Methods:
- A cohort of 247 individuals from the West Midlands, UK, was studied.
- Arterial stiffness was measured using DVP photoplethysmography (PCA 2; Micro Medical).
- Cardiovascular disease risk was assessed using Joint British Society guidelines (JBS2).
Main Results:
- SI strongly correlated with CVD risk (Pearson's R = 0.56, P < 0.001) and increased with risk categories.
- SI demonstrated superior discrimination between low-to-medium and high-risk groups (AUC = 0.76, P < 0.001) compared to traditional risk factors.
- SI effectively identified individuals with known risk factors like diabetes and hypertension.
Conclusions:
- Noninvasive measurement of arterial stiffness using SI may improve CVD risk stratification.
- This approach shows promise for enhancing cardiovascular risk screening in apparently healthy populations.
Background:
Indices of arterial stiffness are accepted as independent markers of cardiovascular disease (CVD), having both positive prognostic and diagnostic implications. The utility of stiffness index (SI) derived from digital volume pulse (DVP) analysis in CVD risk screening is not established.
Methods:
Using a representative sample of individuals from local communities (West Midlands, UK), we determined the performance of SI in the discrimination of increasing CVD risk. Arterial stiffness was measured by DVP photoplethysmography (PCA 2; Micro Medical) using a direct, standardized approach. CVD risk assessment was performed in accordance with the Joint British Society guidelines (JBS2).
Results:
Of our cohort of 247 individuals (51% male; mean age 55.2 (s.d. 10.3) years), 187 were apparently healthy and 60 had established CVD risk factors (diabetes mellitus: 33%, hypertension: 77.8%, hypercholesteremia: 61%). On univariate analysis, SI was strongly associated with CVD risk (the European Society of Cardiology (ESC) based HeartScore) (Pearson correlation coefficient (R): 0.56, P < or = 0.001) and increased in an ordinal fashion from "low risk" to "medium risk" to "high risk" to "very high risk" (pseudo R2 = 0.30; P < 0.001). In receiver operator characteristic curve analysis, SI was the best discriminator between low to medium risk and high-risk categories (area under curve (AUC): 0.76 (95% CI 0.64-0.88), P < 0.001) when compared to total cholesterol, plasma glucose, systolic blood pressure, and waist-to-hip ratio and had the utility to discriminate the individuals with known CVD risk factors such as diabetes and hypertension.
Conclusion:
Noninvasive measurements of arterial stiffness may aid the optimal stratification of CVD risk in an apparently healthy population.
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