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Updated: May 15, 2026

Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Leukocyte and leukocyte subset counts reveal compensatory mechanisms in coronary heart disease
Jingwei Wang1, Jian Song, Junzhu Wu
1Department of Biochemistry, School of Medicine, Wuhan University, Wuhan, 430071, PR China.
Insights
Leukocyte counts in dyslipidaemia patients correlate with LDL cholesterol levels and LDL oxidation. Monocyte-neutrophil interactions may serve as a prognostic factor for coronary heart disease (CHD).
Area of Science:
- Cardiovascular Research
- Immunology
- Metabolic Disorders
Background:
- Leukocyte counts are critical in inflammatory diseases like coronary heart disease (CHD).
- Elevated leukocyte counts correlate with inflammation intensity and poor outcomes.
- This study examines leukocyte subsets in dyslipidaemia and their link to LDL oxidation.
Purpose of the Study:
- Investigate leukocyte and subset counts in dyslipidaemia patients.
- Determine the relationship between leukocyte counts, LDL cholesterol (LDL-C), and LDL oxidation.
- Explore the role of HNP-1 and myeloperoxidase in CHD and dyslipidaemia.
Main Methods:
- Analyzed blood counts and LDL-C in 207 dyslipidaemia patients.
- Compared HNP-1 and myeloperoxidase levels in leukocyte subsets between 24 CHD patients and 24 controls.
- Assessed HNP-1 mRNA levels and myeloperoxidase distribution.
Main Results:
- Total leukocyte and neutrophil counts increased with LDL-C (p=0.001); monocyte counts decreased (p=0.001).
- Neutrophil HNP-1 mRNA levels were significantly higher in CHD patients (2.13-fold), while monocyte levels were lower (p=0.005).
- Myeloperoxidase distribution differed between monocytes and neutrophils.
Conclusions:
- Leukocyte counts and LDL-C levels may be linked to LDL oxidation.
- Monocyte-neutrophil interactions suggest a compensatory mechanism in LDL oxidation in CHD.
- These interactions could be a prognostic indicator for CHD.
Background:
Leukocyte number in the circulation plays a central role in inflammatory diseases, such as coronary heart disease (CHD). Increased counts are correlated with the intensity of the peri-infarction inflammatory response and adverse outcomes. We investigated leukocyte and leukocyte subset counts in dyslipidaemia patients and their relationship with LDL oxidation.
Methods:
Dyslipidaemia patients (207) were selected for blood counts and LDL-C testing. The level of HNP-1and myeloperoxidase in subsets of leukocytes and their relationship with LDL oxidation were compared between 24 CHD patients and 24 normal controls.
Results:
In dyslipidaemia patients, total leukocyte and neutrophil counts increased with LDL-C (p=0.001). Monocyte counts showed the opposite trend (p=0.001). Although serum HNP-1 levels were not different between CHD patients and normal controls (p=0.558), neutrophil HNP-1 mRNA levels were 2.13-fold greater than those of normal controls. However, monocyte HNP-1 mRNA levels were lower (p=0.005). The distribution of myeloperoxidase in monocytes and neutrophils is different, myeloperoxidase locates mainly in the cytoplasm of monocytes, on the cell membrane of neutrophils.
Conclusions:
Leukocyte and leukocyte subset counts may correlate with LDL-C levels and LDL oxidation. The monocyte-neutrophil interaction reveals a potential compensatory mechanism associated with LDL oxidation in CHD that may be a prognostic factor of CHD.
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