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Polysomnography in Bolivian Children Native to High Altitude Compared to Children Native to Low Altitude
Catherine Mary Hill1,2, Annette Carroll3, Dagmara Dimitriou4
1Division of Clinical Experimental Sciences, Faculty of Medicine, University of Southampton, UK.
Insights
High-altitude Andean children exhibit unstable nocturnal oxygen saturation (SpO2) and increased respiratory events, including obstructive hypopnea. This instability may lead to misdiagnosis of sleep-disordered breathing at high altitudes.
Area of Science:
- Pediatric Sleep Medicine
- Altitude Physiology
- Respiratory Medicine
Background:
- High-altitude (HA) native Andean children experience nocturnal oxyhemoglobin saturation (SpO2) instability.
- Understanding SpO2 instability and its impact on sleep quality in these populations is crucial.
Purpose of the Study:
- To compare polysomnographic parameters in high-altitude (HA) native Andean children versus low-altitude (LA) peers.
- To investigate the causes of nocturnal SpO2 instability in HA children.
- To assess the effect of altitude on sleep quality.
Main Methods:
- Recruited 98 healthy children (7-16 years) at LA (500 m) and HA (3,650 m).
- Assessed physical condition and genetic ancestry.
- Conducted attended polysomnography for 58 children at their residential altitude.
Main Results:
- SpO2 was significantly less stable at HA, with greater oxygen desaturation indices.
- Increased obstructive hypopnea and a trend towards central apnea were observed at HA.
- No significant differences in sleep quality were found between altitude groups.
Conclusions:
- HA native Andean children show more respiratory events due to inherent SpO2 instability.
- Standard sleep scoring criteria may overestimate obstructive sleep-disordered breathing at HA.
Study Objectives:
To compare polysomnographic parameters in high altitude (HA) native Andean children with low altitude (LA) native peers in order to explain the nocturnal oxyhemoglobin saturation (SpO2) instability reported in HA native children and to study the effect on sleep quality.
Methods:
Ninety-eight healthy children aged 7-10 y and 13-16 y were recruited at LA (500 m) or HA (3,650 m) above sea level. Physical examination was undertaken and genetic ancestry determined from salivary DNA to determine proportion of European ancestry, a risk factor for poor HA adaptation. Attended polysomnography was carried out over 1 night for 58 children at their resident location.
Results:
Of 98 children recruited, 85 met inclusion criteria, 58 of 85 (68.2%) completed polysomnography, of which 56 were adequate for analysis: 30 at LA (17 male) and 26 at HA (16 male). There were no altitude differences in genetic ancestry, but a high proportion of European admixture (median 50.6% LA; 44.0% HA). SpO2 was less stable at HA with mean 3% and 4% oxygen desaturation indices greater (both P < 0.001) than at LA. This was not explained by periodic breathing. However, more obstructive hypopnea was observed at HA (P < 0.001), along with a trend toward more central apnea (P = 0.053); neither was explained by clinical findings. There was no difference in sleep quality between altitudes.
Conclusions:
HA native Andean children have more respiratory events when scoring relies on SpO2 desaturation due to inherent SpO2 instability. Use of American Academy of Sleep Medicine scoring criteria may yield false-positive results for obstructive sleep-disordered breathing at HA.
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