4.6 Article

Multidisciplinary In-Depth Investigation in a Young Athlete Suffering from Syncope Caused by Myocardial Bridge

期刊

DIAGNOSTICS
卷 11, 期 11, 页码 -

出版社

MDPI
DOI: 10.3390/diagnostics11112144

关键词

athlete; sport activity; laboratory medicine; heart bridge; genomic analysis; exome sequencing; oligogenic combination network

资金

  1. Department of Translational Medical Sciences funds from Paolo Calabro

向作者/读者索取更多资源

Laboratory medicine and genetic investigations play an important role in monitoring athletes' health conditions. This study integrated biochemical, genetic investigations, and advanced imaging techniques to monitor a basketball player's health status, revealing abnormal levels of iron and bilirubin, and the presence of an intramyocardial bridge which may be causing the syncopes. Providing exhaustive personalized diagnostic work up for athletes is crucial for safeguarding their health and preventing irreversible disorders.
Laboratory medicine, along with genetic investigations in sports medicine, is taking on an increasingly important role in monitoring athletes' health conditions. Acute or intense exercise can result in metabolic imbalances, muscle injuries or reveal cardiovascular disorders. This study aimed to monitor the health status of a basketball player with an integrated approach, including biochemical and genetic investigations and advanced imaging techniques, to shed light on the causes of recurrent syncope he experienced during exercise. Biochemical analyses showed that the athlete had abnormal iron, ferritin and bilirubin levels. Coronary Computed Tomographic Angiography highlighted the presence of an intramyocardial bridge, suggesting this may be the cause of the observed syncopes. The athlete was excluded from competitive activity. In order to understand if this cardiac malformation could be caused by an inherited genetic condition, both array-CGH and whole exome sequencing were performed. Array-CGH showed two intronic deletions involving MACROD2 and COMMD10 genes, which could be related to a congenital heart defect; whole exome sequencing highlighted the genotype compatible with Gilbert syndrome. However, no clear pathogenic mutations related to the patient's cardiological phenotype were detected, even after applying machine learning methods. This case report highlights the importance and the need to provide exhaustive personalized diagnostic work up for the athletes in order to cover the cause of their malaise and for safeguarding their health. This multidisciplinary approach can be useful to create ad personam training and treatments, thus avoiding the appearance of diseases and injuries which, if underestimated, can become irreversible disorders and sometimes can result in the death of the athlete.

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