Clinical and biochemical indices of people with high-altitude experience linked to acute mountain sickness.

Travel Med Infect Dis

Institute of Medicine and Equipment for High Altitude Region, College of High Altitude Military Medicine, Army Medical University (Third Military Medical University), Chongqing, 400038, China; Key Laboratory of Extreme Environmental Medicine, Ministry of Education of China, Chongqing, 400038, China; Key Laboratory of High Altitude Medicine, PLA, Chongqing, 400038, China. Electronic address:

Published: December 2022

AI Article Synopsis

  • Acute mountain sickness (AMS) is a significant health issue for travelers at high altitudes, prompting a study to analyze the clinical and biochemical changes in individuals exposed to these conditions.
  • This study involved assessing 14 clinical and 52 biochemical indices in 22 participants before and after ascending to a high altitude of 3648 m, using the Lake Louise Scoring system to diagnose AMS.
  • Results indicated that levels of uric acid and platelet distribution width were significantly higher in individuals resistant to AMS, offering predictive value for susceptibility to AMS, while changes in these indices were associated with the development of AMS.

Article Abstract

Background: Acute mountain sickness (AMS) is a major health issue for people travelling to high altitudes. This study was designed to comprehensively evaluate the changes in clinical characteristics and biochemical indices of high-altitude travelers and determine whether these changes were associated with AMS.

Methods: A total of 14 clinical indices and 52 biochemical indices were determined in 22 subjects before and during acute high-altitude exposure. Six hours after passive ascent to 3648 m (Lhasa, China), the Lake Louise Scoring (LLS) system 2018 was used to assess AMS, which was defined as headache with a total LLS ≥3.

Results: Before travelling to high altitudes, uric acid (UA), platelet distribution width (PDW), mitral peak E velocity (MVE), and ejection fraction (EF) were significantly higher in AMS-resistant individuals than in AMS-susceptible ones (all p < 0.05). A good predictive value of UA (0.817, 95% CI: 0.607-1.000) and PDW (0.844, 95% CI: 0.646-1.000) for AMS-susceptible subjects was found. With high-altitude experience, 14 subjects were diagnosed as having AMS. Compared with non-AMS, the changes in UA and number of neutrophils in AMS presented a significant difference (all p < 0.05). The high-altitude-induced changes in UA, area under the curve, specificity, and sensitivity for identifying AMS were 0.883 (95% CI: 0.738-1.000), 83.30%, and 90.00%, respectively.

Conclusion: Human presents a compensatory physiological and biochemical response to high-altitude travel at early phase. The UA concentration before travel and its trend with high-altitude experience exhibited good performance for identifying AMS.

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Source
http://dx.doi.org/10.1016/j.tmaid.2022.102506DOI Listing

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