SII, SIRI, and MHR as Additional Readings for Personalized Evaluation of Chronic Heart Failure Severity

Edis Baubonis1, Jolanta Laukaitienė2, Ingrida Grabauskytė3

  • 1Medicine Academy, Lithuanian University of Health Sciences, Eiveniu Str. 4, LT-50103 Kaunas, Lithuania.

Insights

In chronic heart failure patients, higher monocyte to HDL ratio (MHR) indicates worsening oxidative stress and cardiac function. The utility of SII and SIRI requires further investigation.

Area of Science:

  • Cardiology
  • Biochemistry
  • Hematology

Background:

  • Chronic heart failure (CHF) is a complex condition with significant morbidity and mortality.
  • Biomarkers reflecting disease severity and underlying pathophysiological processes are crucial for patient management.
  • Neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and monocyte-to-HDL ratio (MHR) are emerging inflammatory markers.

Purpose of the Study:

  • To investigate the relationship between SII, SIRI, and MHR with lipidogram, oxidative stress, and echocardiographic parameters in CHF patients.
  • To determine if SII, SIRI, and MHR can serve as indicators of disease severity and progression in CHF.

Main Methods:

  • A cohort of 220 CHF patients was analyzed.
  • Patients were stratified based on SII, SIRI, and MHR levels.
  • Comprehensive assessments included lipid profiles, oxidative stress markers, and echocardiography.

Main Results:

  • No significant differences in lipidogram, oxidative stress, or echocardiography were found between SII and SIRI groups.
  • Higher MHR was associated with lower HDL, increased left ventricular end-diastolic diameter (LVEDD), left ventricular mass (LVMM), myocardial mass index (MMI), and decreased left ventricular ejection fraction (LVEF).
  • MHR correlated with oxidative stress markers (protein carbonyl, nitrotyrosine) and cardiac remodeling indices (MMI, LVMI).

Conclusions:

  • MHR may serve as a valuable indicator of worsening oxidative stress and cardiac dysfunction in CHF patients.
  • The clinical utility of SII and SIRI in CHF requires further validation.

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