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(Circulation. 2007;115:294-296.)
© 2007 American Heart Association, Inc.

Editorial

Contribution of Long-QT Syndrome Genes to Sudden Infant Death Syndrome

Is It Time to Consider Newborn Electrocardiographic Screening?

Charles I. Berul, MD; James C. Perry, MD

From the Department of Cardiology, Children’s Hospital Boston, Department of Pediatrics, Harvard Medical School, Boston, Mass (C.I.B.), and Section of Pediatric Cardiology, Yale University School of Medicine, New Haven, Conn (J.C.P.).

Correspondence to Charles I. Berul, MD, Department of Cardiology, Children’s Hospital Boston, 300 Longwood Ave, Boston, MA 02115. E-mail charles.berul@cardio.chboston.org

Key Words: Editorials • death, sudden • electrocardiography • genetics • long-QT syndrome • pediatrics • sudden infant death

An extract of the first 250 words of the full text is provided, because this article has no abstract.

	Introduction

 
Sudden infant death syndrome (SIDS) is defined as unexplained and unexpected death within the first year of life, without any known preexisting inciting conditions or obvious cause of death on postmortem examination. It remains the most common cause of infant death (excluding neonatal period) in developed countries, occurring in 0.03% to 0.1% of live-born infants in the United States.¹

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The precise mechanisms for SIDS, or "crib death," are not known, although multiple hypotheses have been proposed over the years, including abnormal brainstem respiratory control of arousal, dysautonomia, and malignant cardiac bradyarrhythmias or tachyarrhythmias.^2–4 Genetic, developmental, and environmental risk factors for SIDS have been identified, such as premature birth, multiple gestations, being the sibling of a SIDS victim, maternal illicit drug use, prone sleeping position or bed sharing, and history of apnea/bradycardia or "near-miss SIDS" episodes.^3–5 Investigators have suggested respiratory control regulatory abnormalities, neurological developmental defects, and cardiac rhythm disorders, including QT prolongation and ventricular arrhythmias, as underpinnings of SIDS. Supporting these various hypotheses are common autopsy findings such as petechial hemorrhages, pulmonary congestion, and developmental defects in the brainstem and neurotransmitters.^4,5 Myriad diagnostic studies have been used for potential risk stratification of infants thought to be at higher risk for SIDS and have included electroencephalogram, pulse oximetry, 12-lead ECG, home apnea monitoring, and infant polysomnography sleep studies. The National Institutes of Health and the American Academy of Pediatrics have actively promoted the supine sleeping position for healthy term infants, and pediatricians have educated parents to put infants . . . [Full Text of this Article]

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				C. Spazzolini, J. Mullally, A. J. Moss, P. J. Schwartz, S. McNitt, G. Ouellet, T. Fugate, I. Goldenberg, C. Jons, W. Zareba, et al. Clinical Implications for Patients With Long QT Syndrome Who Experience a Cardiac Event During Infancy. J. Am. Coll. Cardiol., August 25, 2009; 54(9): 832 - 837. [Abstract] [Full Text] [PDF]

				M. F. O'Rourke Letter by O'Rourke Regarding Articles, "Prevalence of Long-QT Syndrome Gene Variants in Sudden Infant Death Syndrome," "Cardiac Sodium Channel Dysfunction in Sudden Infant Death Syndrome," and "Contribution of Long-QT Syndrome Genes to Sudden Infant Death Syndrome: Is It Time to Consider Newborn Electrocardiographic Screening?" Circulation, July 24, 2007; 116(4): e92 - e92. [Full Text] [PDF]