Identification of Circulating Diagnostic Biomarkers for Coronary Microvascular Disease in Postmenopausal Women Using

Alicia Arredondo Eve1, Elif Tunc1,2, Yu-Jeh Liu1

  • 1Department of Food Science and Human Nutrition, Division of Nutritional Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.

Metabolites
|June 2, 2021
PubMed

Insights

Coronary microvascular disease (CMD) in postmenopausal women can be diagnosed using novel plasma biomarkers. Researchers identified stearic acid and ornithine as potential indicators, offering hope for improved diagnostic tests.

Area of Science:

  • Cardiology
  • Metabolomics
  • Biomarker Discovery

Background:

  • Coronary microvascular disease (CMD) affects postmenopausal women, characterized by heart microvessel dysfunction rather than plaque.
  • Many patients remain undiagnosed or are discharged prematurely, leading to recurrent symptoms.
  • Current diagnostic limitations highlight the need for novel biomarkers.

Purpose of the Study:

  • To identify novel circulating plasma biomarkers for diagnosing CMD in postmenopausal women.
  • To investigate differences in plasma metabolite profiles among healthy women, those with CMD, and those with coronary artery disease (CAD).

Main Methods:

  • Recruited 70 postmenopausal women (26 healthy, 23 CMD, 21 CAD).
  • Conducted comprehensive health screenings, cardiac examinations, and laboratory analyses.
  • Utilized gas chromatography-mass spectrometry (GC-MS) for plasma metabolite profiling and machine learning for biomarker identification.

Main Results:

  • Significantly elevated levels of stearic acid and ornithine were observed in postmenopausal women with CMD.
  • Conversely, valine levels were higher in women diagnosed with CAD.
  • Machine learning approaches successfully identified these distinct metabolite patterns.

Conclusions:

  • Stearic acid and ornithine show potential as circulating biomarkers for CMD in postmenopausal women.
  • These findings could significantly impact the development of future diagnostic tests for CMD.
  • Distinguishing CMD from CAD through metabolic profiling is feasible.

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