Cardiac troponins are highly sensitive and specific biomarkers of cardiac injury and are in a
key role in the diagnosis of acute myocardial infarction (MI). Minor troponin elevations are
common after prolonged strenuous exercise without clinical symptoms of MI or myocardial
injury.
Based on a small gel filtration chromatography study the released troponin in this condition
seems to be predominantly in the form of small fragments. These smaller cytosolic troponin
fragments may more easily traverse across cell membranes that have become leaky but not
irreversibly damaged. Importantly, currently used high-sensitivity troponin T (cTnT) test
detects also smaller troponin fragments which may lead to false diagnosis of MI.
In a Proof-of-Principle study we developed a novel immunoassay which is much simpler and more
sensitive than previously used laboratory methods for studying cTnT fragmentation. In the
present study protocol, we compare the characteristics troponin release after marathon race
and Type 1 MI with the improved version of our novel troponin fragmentation test (SuperTropo
test) and the commercial cTnT test.
A total of 65 recreational runners participating in the 2023 Paavo Nurmi Marathon in Turku
are recruited to the MaraCat2 Study with an open email invitation. All participants give a
blood sample during the post-race visit (within 60 min after finishing the marathon).
A control group of 90 patients with acute Type 1 MI are recruited among patients admitted to
Heart Centre of Turku University Hospital. Coronary angiography is performed in all included
patients to confirm culprit lesion and the MI diagnosis. All included patients are treated
with primary or urgent percutaneous coronary intervention. Only patients with <24 delay from
symptom onset to blood sample are included to avoid the effects of later gradual
fragmentation of cTnT in the circulation.
Certified laboratory services by Turku University Hospital (TYKSLAB) take care of blood
samples. After centrifugation, serum is aliquoted, frozen and stored at -70 °C for later
analysis. Analysis is performed on a single day using the same calibration and set-up to
minimize variation.
cTnT was analyzed using a commercial high-sensitive assay (Roche Diagnostics GmbH, Mannheim,
Germany).
A novel sensitive time-resolved immunofluorometric assay is used for the detection of long
cTnT forms (long cTnT). The long cTnT assay follows the sandwich type immunoassay format and
utilizes time-resolved-fluorescence (TRF) as the measurement platform.
The main aims of the study are:
To assess how often cTnT is elevated after marathon running and which factors affect the cTnT
rise? Is the fragmentation of troponin complex (assessed by long cTnT/ total cTnT ratio) more
common after marathon race compared with Type 1 MI? Is the novel Supertropo test able to
separate exercise-induced troponin elevations from those caused by MI ? All participants
provide written informed consent. The study complies with Declaration of Helsinki as revised
in 2002 and the study protocol was approved by the Medical Ethics Committee of the Hospital
District of Southwest Finland.
Statistical analysis Continuous variables are reported as mean ± standard deviation when
normally distributed, and as median [inter-quartile range (IQR)] if they were skewed unless
stated otherwise. The normality of the data distribution is examined by the Shapiro-Wilk
test. Statistical significance was assumed at a p value < 0.05. Categorical variables were
described with absolute and relative (percentage) frequencies. Chi-squared test and Fisher's
exact test are used for categorical variables as appropriate. Independent samples t-test and
Mann-Whitney U test are used for univariate analysis. Correlation between continuous
variables are estimated using the Spearman test. Linear regression analysis with backward
selection is used to identify factors significantly relating to post-race cTnT levels. All
predictors with a P value < 0.1 in univariate analysis were included in the final regression
model.