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Published on: December 2, 2014
Stiffness index derived from digital volume pulse as a marker of target organ damage in untreated hypertension
Ju-Yi Chen1, Wei-Chuan Tsai, Chih-Chan Lin
1Division of Cardiology, Department of Internal Medicine, National Cheng Kung University Medical Center, Tainan, Taiwan.
Insights
The stiffness index derived from digital volume pulse (SIDVP) correlates with target organ damage in untreated hypertension. This simple index is independently associated with vascular diseases, aiding risk stratification.
Area of Science:
- Cardiovascular physiology
- Biomedical engineering
- Hypertension research
Background:
- Large artery stiffness is a key cardiovascular risk factor.
- Digital Volume Pulse (DVP) analysis offers a non-invasive method to assess arterial properties.
- The Stiffness Index derived from DVP (SIDVP) is a novel index of large artery stiffness.
Purpose of the Study:
- To investigate the role and clinical significance of SIDVP in untreated hypertensive patients.
- To evaluate the association of SIDVP with target organ damage and vascular diseases.
Main Methods:
- 124 untreated hypertensive patients were enrolled.
- Digital Volume Pulse (DVP) was measured using photoplethysmography.
- SIDVP was calculated, alongside aortic stiffness indices (SI, DI), and correlated with clinical markers.
Main Results:
- SIDVP showed significant correlations with blood urea nitrogen (BUN) and left ventricular mass index (LVMI).
- Patients with vascular diseases exhibited higher SIDVP, BUN, and lower distensibility (DI).
- Multivariate analysis identified SIDVP as the sole independent predictor of vascular disease presence (OR 1.39).
Conclusions:
- SIDVP, SI, and DI are correlated with target organ damage in hypertension.
- SIDVP is independently associated with vascular diseases in untreated hypertensive individuals.
- SIDVP derived from DVP is a valuable tool for risk stratification in hypertension.
Objective:
An index of large artery stiffness (SIDVP) simply derived from the digital volume pulse (DVP) was developed recently. However, the role of the SIDVP in untreated hypertensive patients was not well elucidated.
Methods:
We enrolled 124 untreated hypertensive patients (mean age 55.4+/-13.1 years, 57 men). The DVP was measured in right index finger by a photoplethysmography. The SIDVP was formulated as body height divided by transition time from early systolic peak to the inflection point of reflection wave. Two functional indices of aortic compliance, stiffness index (SI) and distensibility (DI), were also used for measurement of aortic stiffness.
Results:
The SIDVP was significantly correlated with blood urea nitrogen (BUN), and left ventricular mass index (LVMI). Patients with vascular diseases had higher level of SIDVP (10.12+/-2.97 vs 8.45+/-1.78, p<0.001), SI (13.76+/-7.63 vs 10.87+/-8.88, p=0.116), BUN (28.4+/-24.7 vs 14.5+/-4.6, p<0.001) and lower level of DI (1.34+/-0.88 vs 1.93+/-1.12, p=0.010) than those without vascular diseases. By multivariate analysis, only the SIDVP was significantly associated with vascular diseases (OR 1.39, 95% CI 1.06-1.82, p=0.016).
Conclusions:
SIDVP, SI and DI were significantly correlated with target organ damage in untreated hypertension. However, only the SIDVP was independently associated with presence of vascular diseases. SIDVP simply derived from the DVP can be used as a marker for risk stratification in untreated hypertensive patients.
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