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Sudden Cardiac Death in Young Athletes March 12, 2013:1027–40
Abbreviations figures with incidence rates rang- in younger athletes, inherited and other acquired cardiovas-
and Acronyms ing from 2.3 to 4.4/100,000 per cular abnormalities are usually responsible (Fig. 1). Cardio-
year (9 –11). myopathy, including HCM and arrhythmogenic right ven-
ARVC ؍arrhythmogenic
right ventricular There is a significant male tricular cardiomyopathy (ARVC), is the most common
cardiomyopathy predominance of SCD among cause of exercise-related SCD (5).
BrS ؍Brugada syndrome athletes. Data from the National Structural cardiac abnormalities. HYPERTROPHIC CARDIO-
CCAA ؍congenital
Center for Catastrophic Sports MYOPATHY. The reported prevalence of HCM is 0.2% in
coronary artery anomaly Injury Research on high school the general population and 0.07% to 0.08% in athletes (17).
ECG ؍electrocardiography and college athletes reported a HCM is a primary myocardial disorder with an autosomal
ER ؍early repolarization
5-fold higher incidence of SCD dominant pattern of inheritance, characterized by left ven-
in male compared with female tricular hypertrophy (LVH) in the absence of abnormal
ESC ؍European Society of
Cardiology athletes (12). In the Veneto re- loading conditions and myocardial disarray on histology.
HCM ؍hypertrophic
gion of northern Italy, where Sudden death due to ventricular tachycardia (VT)/
cardiomyopathy Ͼ110,000 athletes were evalu- ventricular fibrillation (VF) is often the first clinical mani-
ICD ؍implantable
ated over a 21-year follow-up festation (18). Deaths caused by HCM are common in
cardioverter-defibrillator period, the incidence rates of start-stop sports, for example, football and basketball, but
LQTS ؍long QT syndrome SCD were 2.6/100,000 person- rare in endurance events such as rowing, long-distance
LV ؍left ventricular
years in male athletes and 1.1/ cycling, and running. It is hypothesized that the combina-
100,000 person-years in their fe- tion of myocardial hypertrophy, impaired myocardial relax-
LVH ؍left ventricular
hypertrophy male counterparts (2). Several ation, myocardial ischemia, and dynamic left ventricular
LVWT ؍left ventricular
factors are implicated in this sex (LV) outflow obstruction impede augmentation of stroke
wall thickness difference including lower partic- volume for prolonged periods, and individuals with HCM
MVP ؍mitral valve
ipation rates among female ath- are therefore usually selected out of endurance sports.
prolapse letes at the elite level, although The diagnosis is made using electrocardiography (ECG)
PPS ؍pre-participation this trend is changing, and lower and echocardiography. More than 90% of affected individ-
screening prevalence of cardiac abnormali- uals have an abnormal resting electrocardiogram (Figs. 2A
RV ؍right ventricular ties capable of causing SCD in and 2C) (19). All individuals with previous cardiac arrest or
SCD ؍sudden cardiac females (13). sustained VT are at high risk of SCD and require treatment
death Over the past 3 decades, there has with an ICD. Other recognized risk factors for SCD
VF ؍ventricular fibrillation been an explosion in the number of include: 1) unheralded syncope; 2) family history of SCD; 3)
VT ؍ventricular
African/Afro-Caribbean (black) severe LVH (Ͼ30 mm); 4) sustained or nonsustained VT;
tachycardia athletes competing at the elite level and 5) attenuated blood pressure response to exercise. These
(14). SCD appears to be more com- 5 risk factors have low positive predictive value but high
mon in this ethnic group, with a negative predictive value. Subjects exhibiting Ն1 of the 5
reported incidence rate of 5.6/100,000 per year in the United risk markers should be considered for prophylactic insertion
States (11). Cardiomyopathy has been consistently demonstrated of an ICD (20).
as the most common cause of exercise-related SCD in young
athletes. Data from U.S. autopsy series have reported higher death ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY.
rates from hypertrophic cardiomyopathy (HCM) in black com- ARVC has a reported prevalence of 1/1,000 in the general
pared with white athletes (20% vs. 10%, respectively), raising population. It is an inherited myocardial disease caused by
concern that this condition may exhibit a more malignant phe- mutations in genes encoding cardiac desmosomal proteins
notype in black individuals (15). (21). The mechanism of SCD is complex and myocardial
Sudden death occurs more frequently in certain sports. In stretch and myocyte detachment during exercise are thought
the United States, basketball and football have the greatest to result in ventricular arrhythmia and SCD. In survivors,
incidence, whereas in Europe, soccer predominates (16). focal myocarditis with subsequent healing leads to progres-
Extrapolation of this observation suggests that individuals sive fibrofatty replacement of the myocardium and a pro-
participating in sports of high dynamic and low isometric pensity to VT/VF. Macroscopic appearances include right
intensity are at higher risk of death. However, there is the ventricular (RV) dilation, dysfunction, and aneurysm for-
potential for data bias due to higher participation rates in mation (22). Exercise exacerbates these pathophysiological
these sports. changes, and a 5-fold higher risk of SCD in ARVC has
been demonstrated during competitive sports compared
with sedentary activity (2). Diagnosis relies on meeting the
Etiology of SCD in Athletes 2010 ARVC Task Force criteria, which include symptoms,
family history, resting/ambulatory electrocardiographic changes,
In athletes older than 35 years of age, 80% of SCD is echocardiographic and cardiac magnetic resonance imaging
frequently due to atherosclerotic coronary artery disease, but and myocardial tissue characterization (Figs. 2B and 2D)
3. JACC Vol. 61, No. 10, 2013 Chandra et al. 1029
March 12, 2013:1027–40 Sudden Cardiac Death in Young Athletes
Figure 1 Common Causes of Sudden Cardiac Death in Young Athletes
The common causes of SCD in young athletes Ͻ35 years old can be divided into structural, electrical, and acquired cardiac abnormalities (22).
(23). Previous cardiac arrest, unexplained syncope, VT with tomography coronary angiography are the gold standard
hemodynamic compromise and extensive structural disease imaging modalities (27). The usual recommended therapy
including LV involvement are risk factors for SCD and for CCAA is surgical correction; however, there is contro-
should prompt consideration of prophylactic ICD implan- versy regarding which specific types of CCAA require surgical
tation (20,24). correction in an asymptomatic athlete. Although surgery is
almost universally recommended for left-sided CCAA, clinical
CONGENITAL CORONARY ARTERY ANOMALIES. Congenital
management of a right-sided CCAA is more uncertain. It has
coronary artery anomalies (CCAAs) reportedly cause SCD
been suggested that an intramural course, acute-angled take
in 12% to 33% of athletes. The most common anomalies
off, stenosis, or slitlike opening carry higher risk (25).
implicated are left coronary artery origins in the right sinus
of Valsalva and right coronary artery origins in the left sinus OTHER STRUCTURAL CARDIAC ABNORMALITIES. Other struc-
of Valsalva (25). SCD results from ventricular arrhythmia tural cardiac abnormalities associated with SCD include
triggered by myocardial ischemia during exercise. Coronary aortic dissection/rupture typically in the context of Marfan
blood flow is impaired by the abnormal ostium of the syndrome, mitral valve prolapse (MVP), and aortic stenosis.
anomalous vessel, compression of the anomalous artery as it Marfan syndrome is a collagen disorder caused by mutations
courses between the pulmonary artery and ascending aorta, in the gene encoding fibrillin, inherited as an autosomal
and/or coronary spasm triggered by endothelial dysfunction dominant trait with a prevalence of 1 in 5,000. It accounts
(26). Victims of SCD due to CCAA are often asymptom- for approximately 3% of exercise-related SCD in young
atic before presentation, although chest pain associated with athletes and is characterized by skeletal, cardiac, and ocular
syncope should raise suspicion of the disorder. abnormalities. Cystic medial necrosis in the tunica media of the
Diagnosis using ECG, echocardiography, and exercise aorta results in aortic dilation, dissection, or rupture, which
stress testing is notoriously difficult because affected indi- may be expedited by the increases in aortic pressure
viduals rarely reveal features of inducible ischemia during associated with exercise (28,29). Marfan patients should
exercise stress testing or pharmacological functional tests. be prohibited from isometric or isotonic exercise of
Cardiac magnetic resonance angiography and computed moderate to high intensity. Individuals with an enlarged