College of Osteopathic Medicine, Rocky Vista University, Ivins, UT, USA.
J Osteopath Med. 2023 Jun 29;123(10):461-465. doi: 10.1515/jom-2023-0097. eCollection 2023 Sep 1.
Sudden cardiac death (SCD) is a rare yet devastating event that can occur in young athletes. Although hypertrophic obstructive cardiomyopathy is the most common cause of SCD, some other genetic abnormalities have been identified as proarrhythmic. However, there is not routine screening for these other genetic abnormalities. Furthermore, consumption of caffeine, stimulant medication, or prolonged exercise can potentiate the underlying arrhythmic potential. In the event of SCD, advanced cardiac life support (ACLS) should be performed immediately and exactly. The authors present a case of an otherwise healthy young male who collapsed during a marathon and could not be resuscitated despite aggressive measures. After aggressive resuscitative efforts, the patient ultimately expired. A postmortem autopsy revealed no cardiac structural abnormalities, and the cause of death was determined to be cardiac arrhythmia of undetermined etiology. Postmortem genetic testing revealed a heterozygous variation in calcium voltage-gated channel auxiliary subunit beta 2 (CACNB2), a gene associated with arrhythmia and calcium channelopathy. Toxicology showed therapeutic levels of amphetamine. This case highlights the eminent risk of cardiac death in young athletes with proarrhythmic genetic variations, especially in the setting of endurance sport.
心脏性猝死(SCD)是一种罕见但具有毁灭性的事件,可发生于年轻运动员。尽管肥厚型梗阻性心肌病是 SCD 的最常见原因,但已确定其他一些遗传异常具有致心律失常作用。然而,目前并未对这些其他遗传异常进行常规筛查。此外,咖啡因、兴奋剂药物的使用或长时间运动可能会增强潜在的心律失常风险。一旦发生 SCD,应立即且准确地进行高级心脏生命支持(ACLS)。作者报告了一例在马拉松比赛中倒下且尽管采取了积极措施仍无法复苏的年轻健康男性病例。在积极的抢救后,患者最终死亡。尸检显示心脏无结构异常,死因确定为不明原因的心律失常。尸检后的基因检测显示钙电压门控通道辅助亚基β2(CACNB2)存在杂合变异,该基因与心律失常和钙通道病有关。毒理学显示安非他命处于治疗水平。该病例强调了具有致心律失常遗传变异的年轻运动员,尤其是在耐力运动环境中,存在心脏性猝死的巨大风险。