1982
DOI: 10.1016/s0022-3476(82)80009-7
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Arousal responses in near-miss sudden infant death syndrome and in normal infants

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Cited by 139 publications
(42 citation statements)
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“…Data are accumulating that specific genotypes link to impaired brainstem regulation of breathing or other autonomic control as a risk factor for SIDS. Several reports have described near-miss SIDS infants as having a defect in hypercarbic and hypoxic ventilatory arousal responses similar to CCHS patients (Hunt et al 1981;McCulloch et al 1982). The receptor tyrosine kinase RET (rearranged during transfection) proto-oncogene (RET) and the glial cell line-derived neurotrophic factor (GDNF) signaling pathways play significant roles in the development of the respiratory center.…”
Section: Discussionmentioning
confidence: 99%
“…Data are accumulating that specific genotypes link to impaired brainstem regulation of breathing or other autonomic control as a risk factor for SIDS. Several reports have described near-miss SIDS infants as having a defect in hypercarbic and hypoxic ventilatory arousal responses similar to CCHS patients (Hunt et al 1981;McCulloch et al 1982). The receptor tyrosine kinase RET (rearranged during transfection) proto-oncogene (RET) and the glial cell line-derived neurotrophic factor (GDNF) signaling pathways play significant roles in the development of the respiratory center.…”
Section: Discussionmentioning
confidence: 99%
“…12 Furthermore, the arousal response to hypoxic or hypercarbic challenges during sleep may be impaired in both ALTE infants and subsequent siblings of SIDS victims. [13][14][15][16] The majority of SIDS cases occur between 1 and 6 months of age. If arousal deficiency is contributory, seemingly normal developmental changes in infant sleep architecture during this period might act in concert with an arousal deficit to increase an infant's risk.…”
mentioning
confidence: 99%
“…25 Impaired alveolar ventilation and significantly higher arousal thresholds to high CO 2 have also been found in some infants with ALTE. 26 Ventilatory and arousal thresholds to hypercapnia and hypoxia are also increased during sleep and especially during REM sleep. 23,27 In adults, the common response to a single exposure of CO 2 seems to be an enhanced rather than a decreased sensitivity to CO 2 , 28 but this condition has not been studied in infants.…”
Section: Discussionmentioning
confidence: 99%