Identification of novel cardiovascular disease associated metabolites using untargeted metabolomics

Shams Tabrez1,2, Mohammed Razeeth Shait Mohammed3, Nasimudeen R Jabir1,2

  • 1King Fahd Medical Research Center, King Abdulaziz University, P.O. Box 80216, Jeddah 21589, Saudi Arabia.

Insights

This study identified novel metabolites in cardiovascular disease (CVD) patients, offering potential new diagnostic markers and therapeutic targets. These findings enhance our understanding of CVD

Area of Science:

  • Biochemistry
  • Metabolomics
  • Cardiovascular Research

Background:

  • Cardiovascular disease (CVD) is a major global health concern, causing significant morbidity and mortality.
  • Early diagnosis of CVD is crucial for effective management and improved patient outcomes.

Purpose of the Study:

  • To identify novel serum metabolites associated with cardiovascular disease (CVD) using an untargeted metabolomic approach.
  • To explore the potential of these metabolites as diagnostic biomarkers or therapeutic targets for CVD.

Main Methods:

  • Employed an untargeted metabolomic strategy to analyze serum samples from CVD patients and healthy individuals.
  • Utilized statistical analysis to identify significantly differential metabolites.
  • Performed pathway enrichment analysis to understand the metabolic context of identified metabolites.

Main Results:

  • Identified 26 unique metabolites differentially present in CVD patients, with 15 reaching statistical significance.
  • Discovered novel metabolites, including UDP-l-rhamnose and N1-acetylspermidine, not previously linked to CVD.
  • Found that metabolites such as ethanolamide and dimethylarginine can discriminate CVD.
  • Pathway analysis revealed enrichment in histidine metabolism, methyl histidine metabolism, carnitine synthesis, and arginine/proline metabolism in CVD patients.

Conclusions:

  • The study successfully identified unique and novel metabolites associated with cardiovascular disease.
  • These identified metabolites and enriched pathways offer new insights into CVD pathophysiology.
  • The findings present opportunities for developing CVD-specific biomarkers and therapeutic strategies.

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