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Published on: October 12, 2017
HDL-cholesterol is associated with systemic inflammation in cardiac syndrome X
E Tenekecioglu1, M Yilmaz, S Demir
1Department of Cardiology, Bursa Yuksek Ihtisas Education and Research Hospital,Ankara Yolu, Yildirim/Bursa, Bursa, Turkey - erhantenekecioglu@yahoo.com.
Insights
Lower high-density lipoprotein cholesterol (HDL-C) is linked to increased inflammation in cardiac syndrome X (CSX). This suggests investigating HDL-C and inflammatory markers in CSX patients, aiming to raise HDL-C levels.
Area of Science:
- Cardiology
- Inflammation Research
- Metabolic Syndrome
Background:
- Microvascular inflammation is a known factor in cardiac syndrome X (CSX).
- High-density lipoprotein cholesterol (HDL-C) possesses anti-inflammatory properties and supports endothelial function.
- The relationship between HDL-C and inflammatory markers in CSX requires further elucidation.
Purpose of the Study:
- To investigate the association between HDL-C levels and inflammatory markers in patients diagnosed with CSX.
- To determine if lower HDL-C is a predictor of systemic inflammation in CSX.
Main Methods:
- A study involving 100 patients with CSX and 80 healthy controls.
- Evaluation of hematologic indices, lipid profiles, and C-reactive protein (CRP) levels.
- Coronary angiography was performed on all participants.
Main Results:
- CSX patients exhibited significantly higher CRP levels and lower HDL-C compared to controls.
- Increased white blood cell (WBC) count and neutrophil-lymphocyte ratio (NLR) were observed in the CSX group.
- Lower HDL-C levels were identified as a significant independent predictor of higher NLR in CSX patients.
Conclusions:
- Reduced HDL-C is associated with systemic inflammation in individuals with CSX.
- Investigating HDL-C and inflammatory markers is recommended for CSX patients presenting with typical angina and normal coronary arteries.
- Therapeutic strategies aimed at increasing HDL-C levels should be considered for managing CSX.
Aim:
Microvascular inflammation is associated with cardiac syndrome X (CSX). High-density lipoprotein cholesterol (HDL-C) reveals antiatherogenic features with stimulating endothelial NO production, inhibiting oxidative stress and vascular inflammation. We investigated relationship between HDL-C and inflammatory markers in CSX.
Methods:
Hundred patients with CSX and control group of 80 subjects were evaluated. Hematologic indices, lipid levels and C-reactive protein (CRP) levels were studied in patients underwent coronary angiography.
Results:
CRP levels were higher in CSX group than control group (4.59 ± 3.82 mg/dL vs. 2.48 ± 1.32 mg/dL, P<0.001). HDL-C was significantly lower in CSX group compared to control group (36.5 ± 4.0 mg/dL vs. 47.5 ± 12.7 mg/dL, P=0.008). White blood cell (WBC) count was higher in CSX group than in control group. Neutrophil-lymphocyte ratio (NLR) was found significantly increased in CSX group as compared to control group. On multivariate linear regression, lower HDL-C was found to be a significant predictor of higher NLR in patients with CSX independent from other clinical and biochemical variables.
Conclusion:
Lower HDL-C is associated with systemic inflammation in CSX. In patients with typical angina and normal epicardial coronaries,HDL-C and inflammatory markers should be investigated; one of the goals of treatment should be raising HDL-C.
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