Salivary Protein Panel to Diagnose Systolic Heart Failure

Xi Zhang1, Daniel Broszczak2, Karam Kostner3

  • 1Saliva and Liquid Biopsy Translational Research Team, School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Queensland 4059, Australia.

Biomolecules
|November 27, 2019
PubMed

Insights

A new multi-protein biomarker panel in saliva can accurately detect systolic heart failure (SHF). This diagnostic tool shows potential for early SHF detection, improving patient outcomes.

Area of Science:

  • Biomarker Discovery
  • Cardiovascular Diagnostics
  • Proteomics

Background:

  • Screening for systolic heart failure (SHF) presents significant clinical challenges.
  • Current guidelines emphasize SHF prevention and structural heart disease screening.
  • A non-invasive diagnostic medium for SHF detection is highly desirable.

Purpose of the Study:

  • To develop and validate a multi-protein biomarker panel in saliva for SHF detection.
  • To assess the diagnostic accuracy of specific salivary proteins in distinguishing SHF patients from healthy controls.
  • To establish a potential non-invasive biomarker strategy for early SHF identification.

Main Methods:

  • Saliva samples were collected from 100 SHF patients and 88 healthy controls.
  • Enzyme-linked immunosorbent assays (ELISAs) were developed to quantify Kallikrein-1, Protein S100-A7, and Cathelicidin antimicrobial peptide.
  • Analytical and clinical performance of the multi-protein panel was evaluated.

Main Results:

  • The developed immunoassays demonstrated acceptable analytical performance.
  • The multi-protein panel significantly discriminated between SHF patients and healthy controls (p < 0.001).
  • The panel achieved an 81.6% diagnostic accuracy, with 79.2% sensitivity and 85.7% specificity.

Conclusions:

  • A three-protein panel in saliva accurately distinguishes SHF patients from healthy individuals.
  • This salivary biomarker panel shows potential for early detection of systolic heart failure.
  • Further validation in larger cohorts is warranted to confirm clinical utility.

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