The Sudden Infant Death Syndrome (SIDS): A Neuro-Molecular Hypothesis  

Oleh:

Mitterauer, Bernhard ; Garvin, Alex M. ; Dirnhofer, Richard

Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: The Neuroscientist vol. 6 no. 3 (Jun. 2000), page 154–158.
Topik: SIDS; Hyperpolarization activated cation channel; Pacemaker; Mutations; Clock genes
Fulltext: 154TN63.pdf (49.63KB)

Isi artikel

Most of the children who die before age 1 in developed countries do so for unknown reasons, and these deaths are attributed to the sudden infant death syndrome (SIDS). Prospective cardiorespiratory monitoring of infants has revealed that SIDS victims have subtle differences in breathing and heartbeat patterns compared to controls. Because death must involve cardiorespiratory arrest, a straightforward explanation for SIDS is failure on the part of pacemaker neurons controlling the rhythmical processes of breathing or heartbeat. Genes coding for hyperpolarization-activated pacemaker cation channels have recently been isolated and are expressed in the heart and the brain. The authors propose that mutations in these genes and in other genes required for cardiorespiratory pacemaker activity will predispose an individual to SIDS during a window of vulnerability present in the first year of life. Furthermore, mutations in clock genes can alter a variety of rhythmical processes and may indirectly disturb cardiorespiratory function as well.

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