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Hypoxia Induces a Prothrombotic State Independently of the Physical Activity

Hypoxia (oxygen deprivation) is known to be associated with deep vein thrombosis and venous thromboembolism. We attempted to get a better comprehension of its mechanism by going to high altitude, thereby including the potential contributing role of physical activity. Two groups of 15 healthy individ...

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Published in:PloS one 2015-10, Vol.10 (10), p.e0141797-e0141797
Main Authors: Ninivaggi, Marisa, de Laat, Marieke, Lancé, Marcus M D, Kicken, Cécile H, Pelkmans, Leonie, Bloemen, Saartje, Dirks, Marlou L, van Loon, Luc J C, Govers-Riemslag, José W P, Lindhout, Theo, Konings, Joke, de Laat, Bas
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cited_by cdi_FETCH-LOGICAL-c758t-c551193a76f3e2694de641593c710f85a76a2381ee2f734d5efaf31190475f093
cites cdi_FETCH-LOGICAL-c758t-c551193a76f3e2694de641593c710f85a76a2381ee2f734d5efaf31190475f093
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creator Ninivaggi, Marisa
de Laat, Marieke
Lancé, Marcus M D
Kicken, Cécile H
Pelkmans, Leonie
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van Loon, Luc J C
Govers-Riemslag, José W P
Lindhout, Theo
Konings, Joke
de Laat, Bas
description Hypoxia (oxygen deprivation) is known to be associated with deep vein thrombosis and venous thromboembolism. We attempted to get a better comprehension of its mechanism by going to high altitude, thereby including the potential contributing role of physical activity. Two groups of 15 healthy individuals were exposed to hypoxia by going to an altitude of 3900 meters, either by climbing actively (active group) or transported passively by cable car (passive group). Both groups were tested for plasma fibrinogen, von Willebrand factor and factor VIII levels, fibrinolysis, thrombin generating capacity, heart rate, oxygen saturation levels and blood pressure. As a control for the passive group, 7 healthy volunteers stayed immobile in bed for 7 days at normoxic conditions. The heart rate increased and oxygen saturation levels decreased with increasing altitude. Fibrinolysis and fibrinogen levels were not affected. Factor VIII and von Willebrand factor levels levels increased significantly in the active group, but not in the passive group. Plasma thrombin generation remained unchanged in both the active and passive group with increasing altitude and during 7 days of immobility in healthy subjects. However, by applying whole blood thrombin generation, we found an increased peak height and endogenous thrombin potential, and a decreased lagtime and time-to-peak with increasing levels of hypoxia in both groups. In conclusion, by applying whole blood thrombin generation we demonstrated that hypoxia causes a prothrombotic state. As thrombin generation in plasma did not increase, our results suggest that the cellular part of the blood is involved in the prothrombotic phenotype induced by hypoxia.
doi_str_mv 10.1371/journal.pone.0141797
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We attempted to get a better comprehension of its mechanism by going to high altitude, thereby including the potential contributing role of physical activity. Two groups of 15 healthy individuals were exposed to hypoxia by going to an altitude of 3900 meters, either by climbing actively (active group) or transported passively by cable car (passive group). Both groups were tested for plasma fibrinogen, von Willebrand factor and factor VIII levels, fibrinolysis, thrombin generating capacity, heart rate, oxygen saturation levels and blood pressure. As a control for the passive group, 7 healthy volunteers stayed immobile in bed for 7 days at normoxic conditions. The heart rate increased and oxygen saturation levels decreased with increasing altitude. Fibrinolysis and fibrinogen levels were not affected. Factor VIII and von Willebrand factor levels levels increased significantly in the active group, but not in the passive group. Plasma thrombin generation remained unchanged in both the active and passive group with increasing altitude and during 7 days of immobility in healthy subjects. However, by applying whole blood thrombin generation, we found an increased peak height and endogenous thrombin potential, and a decreased lagtime and time-to-peak with increasing levels of hypoxia in both groups. In conclusion, by applying whole blood thrombin generation we demonstrated that hypoxia causes a prothrombotic state. As thrombin generation in plasma did not increase, our results suggest that the cellular part of the blood is involved in the prothrombotic phenotype induced by hypoxia.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26516774</pmid><doi>10.1371/journal.pone.0141797</doi><oa>free_for_read</oa></addata></record>
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1932-6203
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source Open Access: PubMed Central; Publicly Available Content Database
subjects Adult
Air travel
Altitude
Altitude Sickness - blood
Altitude Sickness - physiopathology
Anesthesiology
Anticoagulants
Biochemistry
Blood
Blood coagulation factors
Blood Pressure
Care and treatment
Chronic obstructive pulmonary disease
Climbing
Coagulation factors
Deprivation
Development and progression
Exercise
Family medical history
Female
Fibrinogen
Fibrinogen - metabolism
Fibrinolysis
Generating capacity
Health aspects
Health risk assessment
Heart Rate
High altitude
High-altitude environments
Humans
Hypoxia
Male
Measuring instruments
Metabolism
Middle Aged
Motor Activity
Nutrition
Oxygen
Oxygen content
Patient outcomes
Phenotypes
Physical activity
Physical fitness
Prothrombin - metabolism
Saturation
Studies
Thrombin
Thromboembolism
Thrombosis
Von Willebrand factor
title Hypoxia Induces a Prothrombotic State Independently of the Physical Activity
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