TY - JOUR
T1 - The Role of Genetic Testing in the Identification of Young Athletes with Inherited Primitive Cardiac Disorders at Risk of Exercise Sudden Death
AU - Tiziano, Francesco Danilo
AU - Palmieri, Vincenzo
AU - Genuardi, Maurizio
AU - Zeppilli, Paolo
PY - 2016
Y1 - 2016
N2 - Although relatively rare, inherited primitive cardiac disorders (IPCDs) in athletes have a deep social impact since they often present as sudden cardiac death (SCD) of young and otherwise healthy persons. The diagnosis of these conditions is likely underestimated due to the lack of shared clinical criteria and to the existence of several borderline clinical pictures. We will focus on the clinical and molecular diagnosis of the most common IPCDs, namely hypertrophic cardiomyopathies, long QT syndrome, arrhythmogenic right ventricular cardiomyopathy, and left ventricular non-compaction. Collectively, these conditions account for the majority of SCD episodes and/or cardiologic clinical problems in athletes. In addition to the clinical and instrumental tools for the diagnosis of IPCD, the viral technological advances in genetic testing have facilitated the molecular confirmation of these conditions. However, genetic testing presents several issues: the limited sensitivity (globally, around 50%), the low prognostic predictive value, the probability to find pathogenic variants in different genes in the same patient, and the risk of non-interpretable results. In this review, we will analyze the pros and cons of the different clinical approaches for the presymptomatic identification, the diagnosis and management of IPCD athletes, and we will discuss the indications to the genetic testing for patients and their relatives, particularly focusing on the most complex scenarios, such as presymptomatic tests, uncertain results, and unexpected findings.
AB - Although relatively rare, inherited primitive cardiac disorders (IPCDs) in athletes have a deep social impact since they often present as sudden cardiac death (SCD) of young and otherwise healthy persons. The diagnosis of these conditions is likely underestimated due to the lack of shared clinical criteria and to the existence of several borderline clinical pictures. We will focus on the clinical and molecular diagnosis of the most common IPCDs, namely hypertrophic cardiomyopathies, long QT syndrome, arrhythmogenic right ventricular cardiomyopathy, and left ventricular non-compaction. Collectively, these conditions account for the majority of SCD episodes and/or cardiologic clinical problems in athletes. In addition to the clinical and instrumental tools for the diagnosis of IPCD, the viral technological advances in genetic testing have facilitated the molecular confirmation of these conditions. However, genetic testing presents several issues: the limited sensitivity (globally, around 50%), the low prognostic predictive value, the probability to find pathogenic variants in different genes in the same patient, and the risk of non-interpretable results. In this review, we will analyze the pros and cons of the different clinical approaches for the presymptomatic identification, the diagnosis and management of IPCD athletes, and we will discuss the indications to the genetic testing for patients and their relatives, particularly focusing on the most complex scenarios, such as presymptomatic tests, uncertain results, and unexpected findings.
KW - arrhythmogenic right ventricular displasia
KW - athletes
KW - genetics
KW - hypertrophic cardiomyopathy
KW - isolated non-compact myocardium
KW - long QT syndrome
KW - medical
KW - sudden cardiac death
KW - arrhythmogenic right ventricular displasia
KW - athletes
KW - genetics
KW - hypertrophic cardiomyopathy
KW - isolated non-compact myocardium
KW - long QT syndrome
KW - medical
KW - sudden cardiac death
UR - https://publicatt.unicatt.it/handle/10807/93637
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85043689571&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85043689571&origin=inward
U2 - 10.3389/fcvm.2016.00028
DO - 10.3389/fcvm.2016.00028
M3 - Article
SN - 2297-055X
SP - 28
EP - 28
JO - Frontiers in Cardiovascular Medicine
JF - Frontiers in Cardiovascular Medicine
IS - 3
ER -