Association between blood inflammatory indices and heart failure: a cross-sectional study of NHANES 2009-2018

Yayun Zhang1, Lu Feng2, Zixiong Zhu1

  • 1Department of Cardiovascular Medicine, Third Hospital of Shanxi Medical University, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Taiyuan, China.

Acta Cardiologica
|May 21, 2024
PubMed

Insights

Elevated levels of systemic inflammatory response index (SIRI), neutrophil-to-lymphocyte ratio (NLR), and monocyte-to-lymphocyte ratio (MLR) are linked to a higher risk of heart failure (HF). These complete blood count-derived markers may indicate inflammation associated with HF development.

Area of Science:

  • Cardiovascular Medicine
  • Inflammation Research
  • Hematology

Background:

  • Inflammation is a key factor in the development of heart failure (HF).
  • Complete blood count (CBC)-derived inflammatory biomarkers are increasingly recognized for their potential role in disease pathogenesis.
  • Understanding the association between these biomarkers and HF risk is crucial for early detection and management.

Purpose of the Study:

  • To investigate the association between specific CBC-derived inflammatory biomarkers and the presence of heart failure (HF).
  • To evaluate the potential of systemic immune-inflammation index (SII), systemic inflammatory response index (SIRI), neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and monocyte-to-lymphocyte ratio (MLR) as indicators of HF risk.
  • To explore the nature of the relationship between these inflammatory markers and HF.

Main Methods:

  • Utilized data from the National Health and Nutrition Examination Survey (NHANES) 2009-2018, including 26,021 participants.
  • Compared five CBC-derived inflammatory markers (SII, SIRI, NLR, PLR, MLR) between individuals with and without HF.
  • Employed statistical analyses including smoothing curves, threshold effect analysis, Spearman correlation, and subgroup analyses after adjusting for confounding variables.

Main Results:

  • After adjusting for confounders, SIRI, NLR, and MLR showed significant positive correlations with HF risk.
  • Participants in the highest quarter of SIRI, NLR, and MLR exhibited an increased risk of HF compared to those in the lowest quarter.
  • Subgroup and sensitivity analyses confirmed a stronger correlation between SIRI, NLR, MLR, and HF, with a nonlinear relationship observed.

Conclusions:

  • Elevated levels of SIRI, NLR, and MLR are significantly associated with an increased risk of developing heart failure (HF).
  • These CBC-derived inflammatory markers demonstrate potential utility as systemic inflammation hazard markers for HF.
  • Further research may validate the clinical application of SIRI, NLR, and MLR in HF risk stratification.
Abstract

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