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Published on: October 15, 2010
Direct association between C-reactive protein serum levels and endothelial dysfunction in patients with claudication
J De Haro1, F Acin, A Lopez-Quintana
1Angiology and Vascular Surgery Service, Hospital Universitario Getafe, Madrid, Spain. deharojoaquin@yahoo.es
Insights
High-sensitivity C-reactive protein (hsCRP), an inflammation marker, is elevated in patients with endothelial dysfunction and intermittent claudication. This suggests hsCRP may play a role in peripheral arterial disease development.
Area of Science:
- Cardiovascular Research
- Inflammation Biology
- Vascular Medicine
Background:
- Endothelial dysfunction is a key factor in peripheral arterial disease (PAD) pathogenesis.
- Inflammation plays a significant role in the development and progression of atherosclerosis.
- High-sensitivity C-reactive protein (hsCRP) is a widely recognized marker of systemic inflammation.
Purpose of the Study:
- To investigate the association between hsCRP levels and endothelial dysfunction in patients with intermittent claudication.
- To determine if hsCRP is related to impaired flow-mediated arterial dilation (FMAD) in this patient group.
Main Methods:
- A cross-sectional study involving 156 patients with intermittent claudication was conducted.
- Patients were selected using stratified sampling based on various risk factors.
- Flow-mediated arterial dilation (FMAD) and plasma hsCRP levels were measured to assess endothelial function and inflammation.
Main Results:
- Patients with reduced FMAD (<3%) exhibited significantly higher plasma hsCRP levels compared to those with normal FMAD (>3%).
- A significant negative correlation was observed between hsCRP levels and FMAD (r=-0.465, p<0.05).
- Elevated fibrinogen levels were also associated with impaired endothelial function.
Conclusions:
- Impaired endothelial function in intermittent claudication is linked to increased plasma concentrations of inflammatory markers like hsCRP.
- These findings suggest that inflammation, indicated by hsCRP, may contribute to the underlying mechanisms of peripheral arterial disease.
Objectives:
To evaluate the relationship between C-Reactive Protein (hsCRP), a serum marker of inflammation, and endothelial dysfunction in patients with intermittent claudication.
Design, Patients And Methods:
Cross-sectional study with stratified sampling on dependent variables of age, genre, hypertension, hyperlipidemia, diabetes, smoking status and ankle-brachial index (ABI) to select 156 patients from a target population of 4,100 patients with claudication. We assessed the flow-mediated arterial dilation (FMAD) as a reporter of endothelial function and plasma levels of hsCRP and fibrinogen.
Results:
Patients with a FMAD<3% (range for the lowest 5% of healthy subjects) had increased levels of plasma hsCRP (6.3 vs 2.3mg/L; p<0.05) and fibrinogen (351vs 302mg/L; p<0.05) in comparison to those with FMAD>3%. There was a negative correlation between hsCRP and FMAD(r=-0.465; p<0.05).
Conclusion:
Impaired endothelial dysfunction is association with increased plasma concentrations of inflammatory markers, and both may have a role in the aetiopathogenesis of peripheral arterial disease.
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