Sudden infant death syndrome: Genetic studies in cardiorespiratory and autonomic regulation

Debra E. Weese-Mayer, Elizabeth M. Berry-Kravis, Michael John Ackerman, Mary L. Marazita

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

The 1992 “Back to Sleep” campaign identified modifiable environmental risk factors for sudden infant death syndrome (SIDS) and led to a decrease in SIDS incidence from 1.2 per 1000 live births (1) to 0.529 per 1000 live births in 2003 (2). Despite this decline, African-American infants have a 2.7-fold higher SIDS rate than Caucasian infants (2). This ethnic disparity, coupled with SIDS deaths despite improved compliance with modifiable risk factors, led investigators to consider a genetic basis for SIDS. Thus far, all genetic studies have been based on clinical, neuropathological, and epidemiological observations in SIDS victims, with subsequent identification and study of candidate genes. This chapter focuses exclusively on those genes that are pertinent to cardiorespiratory or autonomic regulation.

Original languageEnglish (US)
Title of host publicationSleep and Breathing in Children
Subtitle of host publicationDevelopmental Changes in Breathing During Sleep, Second Edition
PublisherCRC Press
Pages224-313
Number of pages90
Volume224
ISBN (Electronic)9781420060836
ISBN (Print)9781420060829
StatePublished - Jan 1 2008
Externally publishedYes

ASJC Scopus subject areas

  • Medicine(all)

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  • Cite this

    Weese-Mayer, D. E., Berry-Kravis, E. M., Ackerman, M. J., & Marazita, M. L. (2008). Sudden infant death syndrome: Genetic studies in cardiorespiratory and autonomic regulation. In Sleep and Breathing in Children: Developmental Changes in Breathing During Sleep, Second Edition (Vol. 224, pp. 224-313). CRC Press.