Relation between Systemic Inflammatory Index (SII) and Hair Trace Elements, Metals and Metalloids Concentration in

Tomasz Urbanowicz1, Anetta Hanć1, Anna Olasińska-Wiśniewska1

  • 1Cardiac Surgery and Transplantology Department, Poznan University of Medical Sciences, 61-848 Poznan, Poland.

Insights

Trace elements like lithium, antimony, chromium, and iron in scalp hair correlate with inflammation markers in coronary artery disease (CAD) patients. This study highlights iron

Area of Science:

  • Cardiovascular Medicine
  • Trace Element Analysis
  • Biochemistry

Background:

  • Coronary artery disease (CAD) development involves generic, clinical, lifestyle factors, and inflammation.
  • Investigating trace element concentrations offers insights into pathological processes of CAD.

Purpose of the Study:

  • To explore the relationship between scalp hair trace element concentrations and inflammatory markers in patients with coronary artery disease (CAD).
  • To determine if specific trace elements correlate with systemic inflammation in individuals experiencing anginal symptoms.

Main Methods:

  • Prospective analysis of 35 patients (22 males, 13 females; median age 67 years) with anginal symptoms.
  • Patients were categorized into epicardial coronary artery disease (CAD) and non-CAD groups.
  • Scalp hair chemical analysis and peripheral blood inflammatory markers were assessed.

Main Results:

  • Significant negative correlations were found between hair lithium (Li), antimony (Sb), chromium (Cr), and iron (Fe) concentrations and the systemic inflammatory index (SII) in the CAD group.
  • Specifically, a strong correlation was observed between inflammatory activation and iron concentration in CAD patients.
  • No similar correlations were identified in the non-CAD group.

Conclusions:

  • Scalp hair concentrations of Li, Sb, Cr, and Fe correlate with the systemic inflammatory index (SII) exclusively in patients with coronary artery disease (CAD).
  • Iron concentration demonstrates a strong association with inflammatory activation in individuals with CAD.
Abstract

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