TY - JOUR
T1 - Developmental changes in upper airway dynamics
AU - Marcus, Carole L.
AU - Fernandes Do Prado, Lucila B.
AU - Lutz, Janita
AU - Katz, Eliot S.
AU - Black, Cheryl A.
AU - Galster, Patricia
AU - Carson, Kathryn A.
PY - 2004/7
Y1 - 2004/7
N2 - Normal children have a less collapsible upper airway in response to subatmospheric pressure administration (PNEc) during sleep than normal adults do, and this upper airway response appears to be modulated by the central ventilatory drive. Children have a greater ventilatory drive than adults. We, therefore, hypothesized that children have increased neuromotor activation of their pharyngeal airway during sleep compared with adults. As infants have few obstructive apneas during sleep, we hypothesized that infants would have an upper airway that was resistant to collapse. We, therefore, compared the upper airway pressure-flow (V) relationship during sleep between normal infants, prepubertal children, and adults. We evaluated the upper airway response to 1) intermittent, acute PNEG (infants, children, and adults), and 2) hypercapnia (children and adults). We found that adults had a more collapsible upper airway during sleep than either infants or children. The children exhibited a vigorous response to both PNEG and hypercapnia during sleep (P < 0.01), whereas adults had no significant change. Infants had an airway that was resistant to collapse and showed a very rapid response to P NEG. We conclude that the upper airway is resistant to collapse during sleep in infants and children. Normal children have preservation of upper airway responses to PNEG and hypercapnia during sleep, whereas responses are diminished in adults. Infants appear to have a different pattern of upper airway activation than older children. We speculate that the pharyngeal airway responses present in normal children are a compensatory response for a relatively narrow upper airway.
AB - Normal children have a less collapsible upper airway in response to subatmospheric pressure administration (PNEc) during sleep than normal adults do, and this upper airway response appears to be modulated by the central ventilatory drive. Children have a greater ventilatory drive than adults. We, therefore, hypothesized that children have increased neuromotor activation of their pharyngeal airway during sleep compared with adults. As infants have few obstructive apneas during sleep, we hypothesized that infants would have an upper airway that was resistant to collapse. We, therefore, compared the upper airway pressure-flow (V) relationship during sleep between normal infants, prepubertal children, and adults. We evaluated the upper airway response to 1) intermittent, acute PNEG (infants, children, and adults), and 2) hypercapnia (children and adults). We found that adults had a more collapsible upper airway during sleep than either infants or children. The children exhibited a vigorous response to both PNEG and hypercapnia during sleep (P < 0.01), whereas adults had no significant change. Infants had an airway that was resistant to collapse and showed a very rapid response to P NEG. We conclude that the upper airway is resistant to collapse during sleep in infants and children. Normal children have preservation of upper airway responses to PNEG and hypercapnia during sleep, whereas responses are diminished in adults. Infants appear to have a different pattern of upper airway activation than older children. We speculate that the pharyngeal airway responses present in normal children are a compensatory response for a relatively narrow upper airway.
KW - Children
KW - Critical pressure
KW - Infants
KW - Sleep-disordered breathing
KW - Upper airway collapsibility
UR - http://www.scopus.com/inward/record.url?scp=3042519553&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=3042519553&partnerID=8YFLogxK
U2 - 10.1152/japplphysiol.00462.2003
DO - 10.1152/japplphysiol.00462.2003
M3 - Article
C2 - 14990559
AN - SCOPUS:3042519553
SN - 8750-7587
VL - 97
SP - 98
EP - 108
JO - Journal of applied physiology
JF - Journal of applied physiology
IS - 1
ER -