TY - JOUR
T1 - Sudden death in adults with repaired coarctation of the aorta
T2 - A case for sex-based risk factors
AU - Lastinger, Lauren
AU - Lee, Marc
AU - Hassen, Lauren
AU - Cavus, Omer
AU - Rajpal, Saurabh
AU - Moore, Jeremy P.
AU - Mah, May Ling
AU - Bradley, Elisa A.
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/3
Y1 - 2024/3
N2 - Background: Sudden cardiac death (SCD) is an important risk for adults with repaired coarctation of the aorta (rCoA). We aimed determine if there are clinical risk factors for SCD in adults with rCoA. Methods and results: SCD events and clinical data from all adults with rCoA at a tertiary care center (2007–2017) were evaluated. In 167 adults with rCoA (39 ± 11 years old, 75 (45%) female) SCD occurred in 8 (5%) (vs. age-matched adults 0.9%). Those with SCD demonstrated significant QTc prolongation (QTc: 479 ± 16 vs. 434 ± 30 msec, p < 0.001). Overall, adults with rCoA and a prolonged sex-normative QTc interval had a 12-fold increased risk of SCD (ᵡ2 (1) = 12.3, p < 0.001), with men sustaining SCD at younger ages (42 ± 13 years vs. women 60 ± 10 years, p < 0.05). Multiple logistic regression modeling demonstrated that prolonged QTc selectively advanced risk for SCD in men only (ᵡ2 QTc prolongation 8.46, p < 0.005 and ᵡ2 age 0.29, p = 0.587), whereas in women, age was associated with SCD risk (ᵡ2 QTc prolongation 2.84, p = 0.092 and ᵡ2 age 7.81, p = 0.005). Non-sustained ventricular tachycardia, ventricular dysfunction, and myocardial fibrosis did not significantly impact SCD risk. Conclusions: There is an unanticipated high burden of SCD in adults with rCoA, occurring in men at younger age than women, suspicious for primary electrophysiologic dysfunction. Future investigation of sex-specific SCD risk in rCoA is important to better understand this disease and its late phenotype.
AB - Background: Sudden cardiac death (SCD) is an important risk for adults with repaired coarctation of the aorta (rCoA). We aimed determine if there are clinical risk factors for SCD in adults with rCoA. Methods and results: SCD events and clinical data from all adults with rCoA at a tertiary care center (2007–2017) were evaluated. In 167 adults with rCoA (39 ± 11 years old, 75 (45%) female) SCD occurred in 8 (5%) (vs. age-matched adults 0.9%). Those with SCD demonstrated significant QTc prolongation (QTc: 479 ± 16 vs. 434 ± 30 msec, p < 0.001). Overall, adults with rCoA and a prolonged sex-normative QTc interval had a 12-fold increased risk of SCD (ᵡ2 (1) = 12.3, p < 0.001), with men sustaining SCD at younger ages (42 ± 13 years vs. women 60 ± 10 years, p < 0.05). Multiple logistic regression modeling demonstrated that prolonged QTc selectively advanced risk for SCD in men only (ᵡ2 QTc prolongation 8.46, p < 0.005 and ᵡ2 age 0.29, p = 0.587), whereas in women, age was associated with SCD risk (ᵡ2 QTc prolongation 2.84, p = 0.092 and ᵡ2 age 7.81, p = 0.005). Non-sustained ventricular tachycardia, ventricular dysfunction, and myocardial fibrosis did not significantly impact SCD risk. Conclusions: There is an unanticipated high burden of SCD in adults with rCoA, occurring in men at younger age than women, suspicious for primary electrophysiologic dysfunction. Future investigation of sex-specific SCD risk in rCoA is important to better understand this disease and its late phenotype.
UR - http://www.scopus.com/inward/record.url?scp=85208513594&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85208513594&partnerID=8YFLogxK
U2 - 10.1016/j.ijcchd.2024.100500
DO - 10.1016/j.ijcchd.2024.100500
M3 - Article
C2 - 38550270
AN - SCOPUS:85208513594
SN - 2666-6685
VL - 15
JO - International Journal of Cardiology Congenital Heart Disease
JF - International Journal of Cardiology Congenital Heart Disease
M1 - 100500
ER -