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Circulating HDAC4 reflects lipid profile, coronary stenosis and inflammation in coronary heart disease patients
Zhangli Guo1, Yanqiang Wu1, Qiang Feng1
1Department of Cardiology, HanDan Central Hospital, Handan, 056002, China.
Insights
Histone deacetylase 4 (HDAC4) is decreased in coronary heart disease (CHD) patients, indicating its value in disease monitoring. However, HDAC4 levels do not predict major adverse cardiovascular event risk in these patients.
Area of Science:
- Biochemistry
- Cardiology
- Molecular Biology
Background:
- Coronary heart disease (CHD) poses a significant global health burden.
- Identifying reliable biomarkers for CHD diagnosis and prognosis is crucial.
- Histone deacetylase 4 (HDAC4) role in cardiovascular disease requires further elucidation.
Purpose of the Study:
- To investigate the clinical significance of serum HDAC4 levels in patients with coronary heart disease (CHD).
- To assess the association of HDAC4 with clinical parameters and inflammatory markers in CHD.
- To evaluate the prognostic value of HDAC4 in predicting major adverse cardiovascular events (MACE) in CHD patients.
Main Methods:
- Serum samples were collected from 180 CHD patients and 50 healthy controls.
- Enzyme-linked immunosorbent assay (ELISA) was used to quantify serum HDAC4 levels.
- Statistical analyses were performed to correlate HDAC4 levels with clinical data, inflammatory markers, and MACE.
Main Results:
- Serum HDAC4 levels were significantly lower in CHD patients compared to healthy controls (p < 0.001).
- HDAC4 showed negative correlations with serum creatinine, low-density lipoprotein cholesterol, and C-reactive protein in CHD patients.
- HDAC4 was inversely associated with pro-inflammatory cytokines (TNF-α, IL-1β, IL-6, IL-17A), VCAM1, and the Gensini score.
Conclusions:
- Circulating HDAC4 levels may serve as a valuable biomarker for monitoring disease status in CHD.
- HDAC4 levels were not found to be predictive of major adverse cardiovascular event risk in this cohort.
- Further research is warranted to fully understand the role of HDAC4 in the pathogenesis and progression of CHD.
Abstract:
Aim: To investigate the clinical value of HDAC4 in coronary heart disease (CHD) patients. Methods: The serum HDAC4 levels were determined by ELISA in 180 CHD patients and 50 healthy controls. Results: HDAC4 was decreased in CHD patients compared with healthy controls (p < 0.001). HDAC4 was negatively linked with serum creatinine (p = 0.014), low-density lipoprotein cholesterol (p = 0.027) and C-reactive protein (p = 0.006) in CHD patients. Moreover, HDAC4 was inversely related to TNF-α (p = 0.012), IL-1β (p = 0.002), IL-6 (p = 0.034), IL-17A (p = 0.023), VCAM1 (p = 0.014) and Gensini score (p = 0.001). Unfortunately, neither HDAC4 high (vs low) (p = 0.080) nor HDAC4 quartile (p = 0.268) estimated major adverse cardiovascular event risk. Conclusion: Circulating HDAC4 levels have disease monitoring value but are less valuable in estimating prognosis in CHD patients.
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