Abstract
Objectives:
Ascent to high altitude may result in a hypobaric hypoxic brain injury. The development of acute mountain sickness (AMS) is considered a multifactorial process with hypoxia-induced blood–brain barrier (BBB) dysfunction and resultant vasogenic oedema cited as one potential mechanism. Peripheral S100B is considered a biomarker of BBB dysfunction. This study aims to investigate the S100B release profile secondary to hypoxic brain injury and comment on BBB disturbance and AMS.
Methods:
A prospective field study of 12 subjects who ascended Mt Fuji (3700 m) was undertaken.
Results:
The mean baseline plasma S100B level was 0·11 μg/l (95% CI 0·09–0·12), which increased to 0·22 μg/l (95% CI 0·17–0·27) at the average of three high altitude levels (2590, 3700, and 2590 m on descent) (P < 0·001). The mean level for the seven subjects who experienced AMS rose from 0·10 to 0·19 μg/l compared to 0·12 to 0·25 μg/l for the five subjects who did not develop AMS (P = 0·33).
Conclusion:
Ascending to 3700 m resulted in elevated plasma S100B levels but this was not associated with AMS.
Acknowledgements
We thank the Neurosurgical Nursing Staff at the Royal Brisbane and Women’s Hospital, whose colleagues, family members, and friends volunteered for the study.