Long QT syndrome in neonates: Conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations

• Published in: Journal of the American College of Cardiology Vol. 43; no. 5; pp. 826 - 830
• Main Authors: LUPOGLAZOFF, Jean-Marc, DENJOY, Isabelle, VILLAIN, Elisabeth, FRESSART, Véronique, SIMON, Francoise, BOZIO, André, BERTHET, Myriam, BENAMMAR, Nawal, HAINQUE, Bernard, GUICHENEY, Pascale
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Science 03.03.2004; Elsevier Limited
• Subjects: Age; Biological and medical sciences; Bradycardia; Bradycardia - genetics; Cardiac arrhythmia; Cardiac dysrhythmias; Cardiology; Cardiology. Vascular system; Cation Transport Proteins - genetics; Conduction; Deoxyribonucleic acid; Disorders; DNA; Electrocardiography; Ether-A-Go-Go Potassium Channels; Female; Follow-Up Studies; Heart; Heart rate; Hemodynamics; Humans; Infant, Newborn; Infants; KCNQ Potassium Channels; KCNQ1 Potassium Channel; KCNQ1 protein; Long QT syndrome; Long QT Syndrome - genetics; Male; Medical sciences; Mutation; Neonates; Newborn babies; Parents & parenting; Patients; Potassium Channels - genetics; Potassium Channels, Voltage-Gated; Prognosis; Prolongation; Sinuses; Syncope; Torsades de pointes; Ventricle; Human; Arrhythmia; Prolonged QT interval; Cardiovascular disease; Sinus bradycardia; Phlebology; Conduction disorder; Excitability disorder; Association; Newborn; Heart block; Heart disease; Circulatory system; Mutation; Cardiology
• ISSN: 0735-1097; 1558-3597
• DOI: 10.1016/j.jacc.2003.09.049

We hypothesized that neonatal long QT syndrome (LQTS) with 2:1 atrioventricular block (AVB) could be related to HERG mutations. Early onset of LQTS is rare but carries a high risk of life-threatening events such as ventricular arrhythmias and conduction disorders. There are no data on possible gene specificity. We analyzed the characteristics and outcomes of 23 neonate probands from our LQTS population. Samples of DNA were available in 18 cases. Long QT syndrome was diagnosed because of corrected QT interval (QTc) prolongation (mean QTc of 558 +/- 62 ms) and neonatal bradycardia attributable to sinus bradycardia (n = 8) or 2:1 AVB (n = 15). Symptoms included syncope (n = 2), torsades de pointes (n = 7), and hemodynamic failure (n = 6). Three infants with 2:1 AVB died during the first month of life. During the neonatal period, all living patients received beta-blockers (BB) and 13 had a combination of BB and permanent cardiac pacing. Under treatment, patients remained asymptomatic, with a mean follow-up of seven years. Mutations were identified in HERG (n = 8) and KCNQ1 (n = 8), and one child had three mutations (HERG, KCNQ1, and SCN5A). Conduction disorders were associated with LQT2, whereas sinus bradycardia was associated with LQT1. Two-to-one AVB seems preferentially associated with HERG mutations, either isolated or combined. Long QT syndrome with relative bradycardia attributable to 2:1 AVB has a poor prognosis during the first month of life. In contrast, sinus bradycardia seems to be associated with KCNQ1 mutations, with a good short-term prognosis under BB therapy.