Plasma Ceramides and Cardiovascular Events in Hypertensive Patients at High Cardiovascular Risk

Wenjie Yin1,2,3,4, Fengjuan Li3,4, Xin Tan3,4

  • 1Key Laboratory of Cellular Physiology, Ministry of Education, and the Department of Physiology, Shanxi Medical University, Taiyuan, Shanxi Province, China.

Insights

Plasma ceramides predict cardiovascular events in hypertensive patients. A novel ceramide score (CERT-HBP) improves risk prediction, aiding in identifying high-risk individuals for targeted therapy.

Area of Science:

  • Biochemistry
  • Cardiovascular Medicine
  • Clinical Chemistry

Background:

  • Plasma ceramides (Cer) are established biomarkers for cardiovascular (CV) event risk in coronary heart disease patients.
  • The utility of ceramides and ceramide scores (CERT) for CV risk stratification in hypertensive individuals remains to be fully elucidated.

Purpose of the Study:

  • To investigate the performance of specific plasma ceramides and a novel ceramide score in predicting major adverse cardiovascular events (MACE) among hypertensive patients at high CV risk.

Main Methods:

  • Ultra-performance liquid chromatography-tandem mass spectrometry was used to analyze seven ceramides in 920 essential hypertension patients.
  • Patients were followed for a median of 2.3 years to record MACE, including acute coronary syndrome, heart failure, stroke, and CV death.

Main Results:

  • Three ceramides, Cer(d18:1/16:0), Cer(d18:1/22:0), and Cer(d18:1/24:0), demonstrated significant predictive value for MACE.
  • A novel ceramide score for hypertensive patients (CERT-HBP), incorporating specific ceramides and their ratios, significantly improved the C-statistic from 0.751 to 0.791 (P = 0.010), outperforming traditional risk variables.

Conclusions:

  • A ceramide-based CERT-HBP was developed and validated for evaluating MACE risk in high-risk hypertensive patients.
  • This novel score enhances the identification of patients who may benefit from intensified monitoring and aggressive treatment strategies.
Abstract

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