Utilizing Saliva for Non-Invasive Detection of Exercise-Induced Myocardial Injury with Point-of-Care Cardiac Troponin-I

Abstract

Background Point-of-care (POC) cardiac troponin-I (cTnI) measurement methods often involve immunoassays, which can provide a momentary view of cTnI levels but the current modality highly restricts access to and frequency of testing in a sports and exercise medicine setting due to the requirement of a blood draw.

Objectives This study aimed to compare cTnI concentrations in saliva and serum in athletes before (T1), early (T2), 4 h (T3), and 24 h (T4) after exercise.

Methods 82 male runners were recruited and then divided into two groups. 54 participants (group 1) completed a 5-km time-trial, while 28 participants (group 2) did not undergo this exercise. POC testing device was used to quantify salivary and serum concentrations of cTnI in both groups at T1, T2, T3, and T4.

Results In group 1, salivary and serum concentrations of cTnI increased at T2 (0.41±0.06 ng/mL and 0.48±0.06 ng/mL) compared to T1 (0.18±0.04 ng/mL and 0.22±0.04 ng/mL), reaching the highest values at T3 (0.62±0.05 ng/mL and 0.76±0.05 ng/mL) with the subsequent return to baseline values at T4 (0.16±0.03 ng/mL and 0.22±0.03 ng/mL). In group 2, there were no time-dependent changes in cTnI levels in both saliva (T1: 0.17±0.04 ng/mL, T2: 0.16±0.03 ng/mL, T3: 0.16±0.04 ng/mL, T4: 0.16±0.04 ng/mL) and serum (T1: 0.22±0.04 ng/mL, T2: 0.22±0.04 ng/mL, T3: 0.21±0.03 ng/mL, T4: 0.21±0.04 ng/mL). Salivary and serum concentrations of cTnI were significantly lower in group 2 compared to group 1 at T2 and T3; there was no difference between groups at T1 and T4. Deming regression and Passing–Bablok regression revealed that there was differential bias (at T3), but proportional agreement (at T1, T2, T3, T4) between salivary and serum levels of cTnI in both groups. The Bland–Altman method indicated that there was a negative differential bias but no proportional bias in the data. Recalibration of the new measurement approach (measurement of cTnI levels in saliva) by using the MethodCompare R package was effective in removing existing bias, as evidenced by its similar precision to the reference method (measurement of cTnI levels in serum), particularly at T2, T3, and T4.

Conclusions In athletic settings, quantification of cTnI levels in saliva utilizing the POC-cTnI-Getein1100 assay may be a useful non-invasive tool in evaluating whether exercise-induced increases in cTnI levels are transient or there are acutely or chronically elevated cTnI concentrations.

FigureFigureCompeting Interest Statement

The authors have declared no competing interest.

Funding Statement

This study was funded by the Russian Science Foundation [project number 23-75-01039, https://rscf.ru/en/project/23-75-01039/].

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Bioethics Committee of Lobachevsky University gave ethical approval for this work.

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Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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Yes

Data availability statement

Data will be made available on request.

Abbreviations and AcronymsAMIacute myocardial infarctionCIconfidence intervalcTncardiac troponincTnIcardiac troponin-IcTnTcardiac troponin-TOLSordinary least squaresPOCpoint-of-careSDstandard deviationSCDsudden cardiac death

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