Impact of the metabolic syndrome and its components on pulse wave velocity
1Department of Internal Medicine, Dongguk University College of Medicine, Gyeongju, Korea. ykkim@duih.org
Insights
Metabolic syndrome (MS) components, particularly elevated blood pressure, are linked to arterial stiffness. The clustering of MS factors, not individual components, significantly impacts pulse wave velocity (PWV), a marker of cardiovascular risk.
Area of Science:
- Cardiovascular Medicine
- Vascular Physiology
- Metabolic Disorders
Background:
- Pulse wave velocity (PWV) is a key indicator of arterial stiffness and cardiovascular disease (CVD) risk.
- Metabolic syndrome (MS) components are known CVD risk factors, but their specific impact on PWV is not fully understood.
Purpose of the Study:
- To investigate the association between individual and clustered components of the metabolic syndrome (MS) and pulse wave velocity (PWV).
- To determine if MS components independently affect arterial stiffness.
Main Methods:
- Simultaneous measurement of heart-femoral (hfPWV) and brachial-ankle (baPWV) using an automatic waveform analyzer in 364 subjects without clinical CVD or diabetes.
- Analysis of associations between PWV and individual/clustered MS features.
Main Results:
- Univariate analysis showed most MS components, except low HDL-cholesterol, were associated with increased hfPWV and baPWV.
- Multivariate analysis revealed only elevated blood pressure (BP) as an independent factor for PWV.
- PWV increased with the number of MS components present (p < 0.001), and MS was associated with increased baPWV after controlling for age, gender, and BP (p < 0.05).
Conclusions:
- Individual MS components, except elevated BP, do not independently affect arterial stiffness.
- The clustering of MS components may synergistically increase arterial stiffness, highlighting the importance of managing multiple risk factors.
Background:
Pulse wave velocity (PWV) reflects arterial stiffness and may provide an integrated index of vascular status and cardiovascular disease (CVD) risk. Although the individual components of the metabolic syndrome (MS) are well established cardiovascular risk factors, the impact of the MS and its components on PWV has not been well defined.
Methods:
Using an automatic wave form analyzer, heart-femoral (hf) and brachial-ankle (ba) PWVs were measured simultaneously in 364 subjects (age, 44.8 +/- 9.3 years). None of the subjects had clinical atherosclerotic CVD, diabetes, or systemic disease. The association between PWVs and the features of the MS, individual and clustered, were analyzed.
Results:
By univariate analysis, the individual components of the MS, except for a low HDL-cholesterol level, were associated with increased hfPWV and baPWV. Hypercholesterolemia was also associated with increase in both PWVs. A low HDL-cholesterol level was associated with an increased baPWV. However, by multivariate analysis, none of the components of the MS, except for an elevated blood pressure (BP), was an independent factor affecting hfPWV and baPWV. After controlling for age and gender, hfPWV and baPWV were increased according to the number of MS components present (p < 0.001 for both). After controlling for age, gender and BP, the MS was associated with an increased baPWV (p < 0.05).
Conclusions:
The clustering of MS components may interact to synergistically affect arterial stiffness, even though the individual MS components, except for an elevated BP, do not affect arterial stiffness independently.
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