Literature DB >> 15142636

Sudden death among infants and adults: companion disorders of maladaptive sympathetic bias.

Anthony J Yun1, Patrick Y Lee.   

Abstract

Sudden infant death syndrome is the leading cause of death in infancy, but its pathophysiological mechanism has been elusive. Sudden death in adults is a common phenomenon, but the etiology in many cases remains unknown at autopsy. We hypothesize that maladaptive sympathetic bias is the explanatory mechanism that links many cases of sudden demise among adults and infants as companion syndromes. Normally, sympathetic response occurs as an adaptation to physiologic demands of the body through various autonomic reflex arcs such as chemoreceptors. Sympathetic response can become chronic and maladaptive when the normal sympathetic response fails to correct the precipitating physiologic trigger, leading to chronic activation of autonomic reflex arcs. In conditions such as infant sleep apnea or adult heart failure, a pernicious cycle of sympathetic bias may result. Chronic sympathetic bias increases susceptibility to sudden fatal arrhythmias, QT-related and otherwise, in the setting of an exaggerated adrenergic challenge. Examples of such adrenergic stressors include trauma, hypoxia, hypercapnia, acidosis, sleep arousal, illness, medical procedures, and physical activity, all of which have associations with sudden death. Our hypothesis may not only help explain the survival benefits of drugs such as beta-blockers and devices such as synchronization therapy, but also portend new application of similar therapies for many conditions of sympathetic bias.

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Year:  2004        PMID: 15142636     DOI: 10.1016/j.mehy.2003.11.014

Source DB:  PubMed          Journal:  Med Hypotheses        ISSN: 0306-9877            Impact factor:   1.538


  4 in total

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Authors:  David J Tester; Michael J Ackerman
Journal:  Pediatr Cardiol       Date:  2012-02-04       Impact factor: 1.655

2.  Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndrome.

Authors:  David J Tester; Bi-Hua Tan; Argelia Medeiros-Domingo; Chunhua Song; Jonathan C Makielski; Michael J Ackerman
Journal:  Circ Cardiovasc Genet       Date:  2011-08-11

3.  Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.

Authors:  David J Tester; Leonie C H Wong; Pritha Chanana; Belinda Gray; Amie Jaye; Jared M Evans; Margaret Evans; Peter Fleming; Iona Jeffrey; Marta Cohen; Jacob Tfelt-Hansen; Michael A Simpson; Elijah R Behr; Michael J Ackerman
Journal:  J Pediatr       Date:  2018-09-26       Impact factor: 4.406

4.  Loss of the transcription factor Meis1 prevents sympathetic neurons target-field innervation and increases susceptibility to sudden cardiac death.

Authors:  Fabrice Bouilloux; Jérôme Thireau; Stéphanie Ventéo; Charlotte Farah; Sarah Karam; Yves Dauvilliers; Jean Valmier; Neal G Copeland; Nancy A Jenkins; Sylvain Richard; Frédéric Marmigère
Journal:  Elife       Date:  2016-02-08       Impact factor: 8.140

  4 in total

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