Lauren Lastinger , Marc Lee , Lauren Hassen , Omer Cavus , Saurabh Rajpal , Jeremy P. Moore , May Ling Mah , Elisa A. Bradley
{"title":"成人主动脉瓣闭锁修复后猝死:基于性别的风险因素案例","authors":"Lauren Lastinger , Marc Lee , Lauren Hassen , Omer Cavus , Saurabh Rajpal , Jeremy P. Moore , May Ling Mah , Elisa A. Bradley","doi":"10.1016/j.ijcchd.2024.100500","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>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.</p></div><div><h3>Methods and results</h3><p>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 (ᵡ<sup>2</sup> (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 (ᵡ<sup>2</sup> QTc prolongation 8.46, p < 0.005 and ᵡ<sup>2</sup> age 0.29, p = 0.587), whereas in women, age was associated with SCD risk (ᵡ<sup>2</sup> QTc prolongation 2.84, p = 0.092 and ᵡ<sup>2</sup> age 7.81, p = 0.005). Non-sustained ventricular tachycardia, ventricular dysfunction, and myocardial fibrosis did not significantly impact SCD risk.</p></div><div><h3>Conclusions</h3><p>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.</p></div>","PeriodicalId":73429,"journal":{"name":"International journal of cardiology. Congenital heart disease","volume":"15 ","pages":"Article 100500"},"PeriodicalIF":0.8000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666668524000090/pdfft?md5=7e0c04ba5221cb10eaa83d1c6111cf01&pid=1-s2.0-S2666668524000090-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Sudden death in adults with repaired coarctation of the aorta: A case for sex-based risk factors\",\"authors\":\"Lauren Lastinger , Marc Lee , Lauren Hassen , Omer Cavus , Saurabh Rajpal , Jeremy P. Moore , May Ling Mah , Elisa A. Bradley\",\"doi\":\"10.1016/j.ijcchd.2024.100500\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>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.</p></div><div><h3>Methods and results</h3><p>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 (ᵡ<sup>2</sup> (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 (ᵡ<sup>2</sup> QTc prolongation 8.46, p < 0.005 and ᵡ<sup>2</sup> age 0.29, p = 0.587), whereas in women, age was associated with SCD risk (ᵡ<sup>2</sup> QTc prolongation 2.84, p = 0.092 and ᵡ<sup>2</sup> age 7.81, p = 0.005). Non-sustained ventricular tachycardia, ventricular dysfunction, and myocardial fibrosis did not significantly impact SCD risk.</p></div><div><h3>Conclusions</h3><p>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.</p></div>\",\"PeriodicalId\":73429,\"journal\":{\"name\":\"International journal of cardiology. 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Sudden death in adults with repaired coarctation of the aorta: A case for sex-based risk factors
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.