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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.
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.
Abstract:
Screening for systolic heart failure (SHF) has been problematic. Heart failure management guidelines suggest screening for structural heart disease and SHF prevention strategies should be a top priority. We developed a multi-protein biomarker panel using saliva as a diagnostic medium to discriminate SHF patients and healthy controls. We collected saliva samples from healthy controls (n = 88) and from SHF patients (n = 100). We developed enzyme linked immunosorbent assays to quantify three specific proteins/peptide (Kallikrein-1, Protein S100-A7, and Cathelicidin antimicrobial peptide) in saliva samples. The analytical and clinical performances and predictive value of the proteins were evaluated. The analytical performances of the immunoassays were all within acceptable analytical ranges. The multi-protein panel was able to significantly (p < 0.001) discriminate saliva samples collected from patients with SHF from controls. The multi-protein panel demonstrated good performance with an overall diagnostic accuracy of 81.6% (sensitivity of 79.2% and specificity of 85.7%) when distinguishing SHF patients from healthy individuals. In conclusion, we have developed immunoassays to measure the salivary concentrations of three proteins combined as a panel to accurately distinguish SHF patients from healthy controls. While this requires confirmation in larger cohorts, our findings suggest that this three-protein panel has the potential to be used as a biomarker for early detection of SHF.
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