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The Diagnostic Significance of Circulating Eicosanoid in Patients with Hypertrophic Cardiomyopathy
Yue Zhang1, Xinyu Liu1, Zhongze Zhang1
1Tianjin Key Laboratory of Metabolic Diseases, The Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, Center for Cardiovascular Diseases, Research Center of Basic Medical Sciences, Department of Physiology and Pathophysiology, Tianjin Medical University, Tianjin, China.
Insights
Hypertrophic cardiomyopathy (HCM) patients show lower levels of key eicosanoids, essential molecules involved in cardiovascular health. Specific eicosanoids like 12-HETE and EPA can help diagnose this hereditary heart disease.
Area of Science:
- Biochemistry
- Cardiovascular Medicine
- Metabolomics
Background:
- Hypertrophic cardiomyopathy (HCM) is a prevalent hereditary cardiovascular disease.
- Eicosanoids are significant in cardiovascular diseases and function as biomarkers.
Purpose of the Study:
- To profile plasma eicosanoids in HCM patients and healthy individuals.
- To identify eicosanoids as potential biomarkers for HCM diagnosis.
- To explore the relationship between eicosanoids and clinical markers in HCM.
Main Methods:
- Plasma eicosanoids were profiled using liquid chromatography-mass spectrometry (LC-MS).
- A cohort of 73 HCM patients and 78 healthy individuals was analyzed.
- Metabolic network analysis and correlation studies were performed.
Main Results:
- HCM patients exhibited downregulation of various eicosanoids, including arachidonic acid (AA), 5,6-DHET, 12-HETE, lipoxin A4 (LXA4), and eicosapentaenoic acid (EPA).
- A predictive model using 12-HETE and EPA showed significant diagnostic value for HCM.
- Eicosanoids like 17,18-EEQ, LXA4, and 13-oxo-ODE negatively correlated with hs-CRP and NT-proBNP levels in patients.
Conclusions:
- Alterations in eicosanoid metabolism are implicated in the pathophysiology of HCM.
- Specific eicosanoids, such as 12-HETE and EPA, hold potential as diagnostic biomarkers for HCM.
- Eicosanoid profiles may offer insights into disease severity and associated inflammatory markers in HCM.
Abstract:
Hypertrophic cardiomyopathy (HCM) is one of the most prevalent hereditary cardiovascular diseases. Eicosanoids are known to play a significant role in cardiovascular diseases and serve as biomarkers. In this study, plasma eicosanoids were profiled by LC-MS in a cohort of 78 healthy individuals and 73 patients diagnosed with HCM. Our findings reveal HCM patients exhibit downregulation of various eicosanoids, including AA, 5,6-DHET, 12-HETE, LXA4, EPA, etc. Notably, the combined predictive model incorporating 12-HETE and EPA demonstrates significant diagnostic value for HCM. Additionally, ten closely related metabolites showed significant positive correlations within the metabolic network graph. Eicosanoids such as 17,18-EEQ, LXA4, and 13-oxo-ODE exhibit significant negative correlations with plasma concentrations of hs-CRP and NT-proBNP in patients. Alterations in eicosanoid metabolism may be implicated in the pathophysiological processes underlying HCM.
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