Familial clustering of cardiac conditions in patients with anomalous aortic origin of a coronary artery and myocardial bridges

• Published in: Cardiology in the young Vol. 28; no. 9; pp. 1099 - 1105
• Main Authors: Agrawal, Hitesh, Mery, Carlos M., Sexson Tejtel, S. Kristen, Fraser, Charles D., McKenzie, E. Dean, Qureshi, Athar M., Molossi, Silvana
• Format: Journal Article
• Language: English
• Published: Cambridge, UK Cambridge University Press 01.09.2018
• Subjects: Algorithms; Anomalies; Aorta; Arrhythmia; Arteriosclerosis; Atherosclerosis; Athletes; Bridges; Cardiology; Cardiomyopathy; Cardiovascular disease; Children; Clustering; Congenital diseases; Coronary artery; Coronary artery disease; Coronary vessels; Death; Families & family life; Family medical history; Genetics; Heart; Heart diseases; Marfan syndrome; Mortality; Original Article; Pain; Patients; Siblings; Sinuses; Surgery; Thoracic surgery; Veins & arteries; United States > US; Vallejo California; Texas; myocardial bridge; Anomalous coronary artery
• DOI: 10.1017/S1047951118000835
• ISSN: 1047-9511

Anomalous aortic origin of a coronary artery is the second leading cause of sudden cardiac arrest/death in young athletes in the United States of America. Limited data are available regarding family history in this patient population. Patients were evaluated prospectively from 12/2012 to 02/2017 in the Coronary Anomalies Program at Texas Children's Hospital. Relevant family history included the presence of CHD, sudden cardiac arrest/death, arrhythmia/pacemaker use, cardiomyopathy, and atherosclerotic coronary artery disease before the age of 50 years. The presence of one or more of these in 1st- or 2nd-degree relatives was considered significant. Of 168 unrelated probands (171 patients total) included, 36 (21%) had significant family history involving 19 (53%) 1st-degree and 17 (47%) 2nd-degree relatives. Positive family history led to cardiology referral in nine (5%) patients and the presence of abnormal tests/symptoms in the remaining patients. Coronary anomalies in probands with positive family history were anomalous right (27), anomalous left (five), single right coronary artery (two), myocardial bridge (one), and anomalous circumflex coronary artery (one). Conditions present in their family members included sudden cardiac arrest/death (15, 42%), atherosclerotic coronary artery disease (14, 39%), cardiomyopathy (12, 33%), CHD (11, 31%), coronary anomalies (3, 8%), myocardial bridge (1, 3%), long-QT syndrome (2, 6%), and Wolff-Parkinson-White (1, 3%). In patients with anomalous aortic origin of a coronary artery and/or myocardial bridges, there appears to be familial clustering of cardiac diseases in approximately 20% of patients, half of these with early occurrence of sudden cardiac arrest/death in the family.