scholarly journals Acute Mountain Sickness Following Incremental Trekking to High Altitude: Correlation With Plasma Vascular Endothelial Growth Factor Levels and the Possible Effects of Dexamethasone and Acclimatization Following Re-exposure

2021 ◽  
Vol 12 ◽  
Author(s):  
Craig Winter ◽  
Tracy Bjorkman ◽  
Stephanie Miller ◽  
Paul Nichols ◽  
John Cardinal ◽  
...  

Purpose: The recognition and treatment of high-altitude illness (HAI) is increasingly important in global emergency medicine. High altitude related hypobaric hypoxia can lead to acute mountain sickness (AMS), which may relate to increased expression of vascular endothelial growth factor (VEGF), and subsequent blood-brain barrier (BBB) compromise. This study aimed to establish the relationship between AMS and changes in plasma VEGF levels during a high-altitude ascent. VEGF level changes with dexamethasone, a commonly used AMS medication, may provide additional insight into AMS.Methods: Twelve healthy volunteers ascended Mt Fuji (3,700 m) and blood samples were obtained at distinct altitudes for VEGF analysis. Oxygen saturation (SPO2) measurements were also documented at the same time-point. Six out of the 12 study participants were prescribed dexamethasone for a second ascent performed 48 h later, and blood was again collected to establish VEGF levels.Results: Four key VEGF observations could be made based on the data collected: (i) the baseline VEGF levels between the two ascents trended upwards; (ii) those deemed to have AMS in the first ascent had increased VEGF levels (23.8–30.3 pg/ml), which decreased otherwise (23.8–30.3 pg/ml); (iii) first ascent AMS participants had higher VEGF level variability for the second ascent, and similar to those not treated with dexamethasone; and (iv) for the second ascent dexamethasone participants had similar VEGF levels to non-AMS first ascent participants, and the variability was lower than for first ascent AMS and non-dexamethasone participants. SPO2 changes were unremarkable, other than reducing by around 5% irrespective of whether measurement was taken for the first or second ascent.Conclusion: First ascent findings suggest a hallmark of AMS could be elevated VEGF levels. The lack of an exercise-induced VEGF level change strengthened the notion that elevated plasma VEGF was brain-derived, and related to AMS.

2006 ◽  
Vol 17 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Joseph Palma ◽  
Christian Macedonia ◽  
Patricia Deuster ◽  
Cara Olsen ◽  
B. Robert Mozayeni ◽  
...  

CHEST Journal ◽  
2000 ◽  
Vol 118 (1) ◽  
pp. 47-52 ◽  
Author(s):  
James Maloney ◽  
Dale Wang ◽  
Timothy Duncan ◽  
Norbert Voelkel ◽  
Stephen Ruoss

2007 ◽  
Vol 30 (3) ◽  
pp. 42
Author(s):  
Vy-Van Le ◽  
Michel White ◽  
Rhian Touyz ◽  
Heather Ross ◽  
Yves Tessier ◽  
...  

Background: Exposure to hypobaric hypoxemia causes acute mountain sickness (AMS) in 40% of subjects acutely exposed to an altitude of 4,000 m. Vascular endothelial growth factor (VEGF) and cytokines appear to play a role in AMS in model systems. The objective of this pilot study was to explore the change in VEGF, the vasodilatory prostacyclin PGI-2, interleukin-6 and thiobarbituric acid reactive substances (TBARS) levels following prolonged exposure to hypobaric hypoxemia on Bolivian Altiplano. The secondary objective was to investigate the relationship between these markers with good versus poor adaptation to high altitude. Methods: The study population consisted of 7 climbers aged 24-64 yr. One cardiac transplant and one kidney transplant recipients participated in this study. Aerobic capacity was assessed on a treadmill using a RAMP protocol with gas exchange analyses. Blood samples were harvested within 48 hr of departure and within 24 hr returning to sea level. Results: Selected biochemisty parameters are presented in the table: *** Table in Full Text PDF. *** Data are mean ±SD. CP= cardiopulmonary. Both cardiac and Tx recipients did not experience AMS. Maximum altitude achieved: ∗6120-6522; †5680; ‡5300 meters. Conclusions: Pulmonary maladaptation to high altitude results in a 2-fold elevated VEGF and PGI-2 without concomitant increase of markers of inflammation or oxidative stress. VEGF does not appear to increase in cerebral maladaptation to high altitude. Further investigations are needed to better understand the role of VEGF and other biomarkers during the process of adaptation or maladaptation to high altitude.


2007 ◽  
Vol 101 (3) ◽  
pp. 587-594 ◽  
Author(s):  
David A. Dorward ◽  
A.A. Roger Thompson ◽  
J. Kenneth Baillie ◽  
Margaret MacDougall ◽  
Nikhil Hirani

2013 ◽  
Vol 5 (1) ◽  
pp. e2013044 ◽  
Author(s):  
Sameh Samir Fahmey ◽  
Hassan Naguib ◽  
Sanna Abdelshafy ◽  
Rasha Alashry

Background: The β-Thalassemia syndromes are the most common hereditary chronic hemolytic anemia due to impaired globin chain synthesis.  Vascular endothelial growth factor (VEGF) plays several roles in angiogenesis which is a crucial process in the pathogenesis of several inflammatory, autoimmune and malignant diseases .Endothelial damage and inflammation make a significant contribution to the pathophysiology of β-thalassemia. Purpose: The aim of the study was to assess serum VEGF level in children with beta-thalassemia major as a marker of angiogenesis. Methods: Blood samples were collected from 40 patients with thalassemia major and 10 healthy controls and assayed for VEGF by enzyme-linked immunosorbent assay. Results: VEGF level was significantly higher in patients with β-Thalassemia major than healthy controls (p=0.001).In addition, VEGF level was higher in splenectomised thalassemic patients than non splenectomised ones (p=0.001) .However, there were a positive correlation between VEGF and chelation starting age (p=0.008) and a negative correlation between VEGF and frequency of blood transfusion (p=0.002). Conclusion: thalassemia patients, especially splenectomized, have elevated serum levels of VEGF. Early chelation and regular blood transfusion help to decrease serum VEGF and the risk of angiogenesis.  


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