High Altitude Medical Research Expedition Himlung 2013 - a Study of Human Adaption to Hypoxia

Hypoxia Clinical Trial

— HiReach 2013  

Official title:

High Altitude Medical Research Expedition Himlung 2013 - an Observational Cohort Study of Human Adaption to Hypobaric Hypoxia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01953198
• Other study ID #: 226/12
• Status: Completed
• Phase: N/A
• First received: September 25, 2013
• Last updated: September 25, 2013
• Start date: December 2012
• Est. completion date: June 2013

Study information

• Verified date: September 2013
• Source: University Hospital Inselspital, Berne
• Contact: n/a
• Is FDA regulated: No
• Health authority: Switzerland: Ethikkommission
• Study type: Observational

Clinical Trial Summary

The aim of the project "High Altitude Medical Research Expedition Himlung 2013" (HiReach2013) is to comprehensively investigate the cerebral, cardiovascular and pulmonary adaptation and the reactions of the human immune system during an ascent to extreme altitudes of over 7000 m. A total of 44 healthy and trained volunteers will be included in the study after written informed consent has been obtained.Baseline sea level clinical examination will be performed in Bern, Switzerland (BE1) at 550 m 8 to 4 weeks before departure. High altitude research facilities will be available at the altitudes of 5000m, 6100m and 6900m. Post-expedition examination will be performed within 2 to 6 weeks after the end of the expedition in Bern. In the context of 3 sub-projects specific measurements and examinations are performed.

These include: cMRI before and after the climb and neurovascular doppler examination during the climb; blood sampling for coagulation studies, cardiac and thoracic ultrasound, stress tests for assessment of cardiovascular performance.

Description:

Background

Altitude related medical problems are gaining more importance and attention as an ever increasing number of people travel to higher altitudes for work or pleasure. Resort towns in Europe and the Western United States at elevations in the 2000 m to 3000 m range attract millions of visitors annually. Many more visit cities in South America and Asia situated above 3000 m. In addition, tens of thousands of travelers, trekkers, and skiers worldwide ascend to elevations in the range of 3000 to 5500 m. An ever-increasing number of recreational climbers attempt ascents of summits of very high (3500 m to 5500 m) or extreme (>5500 m) altitudes. The Nepalese Ministry of Tourism and Civil Aviation and the Nepal Mountaineering Association reported having issued permits to 6032 climbers for peaks higher than 6000 m in the year 2010 alone. When considering that the number of people residing at high altitude is bound to increase, it is of importance to further deepen our understanding of the physiologic changes and dangers associated with exposure to high altitude. Oxygen homeostasis is essential for survival of healthy humans at high altitudes. Various physiological changes involving different organ systems occur during exposition and acclimatization to hypobaric hypoxia in the context of a high altitude sojourn. These include marked adaptations of pulmonary and systemic vascular function, changes in cerebral perfusion and metabolism, physiologic and metabolic adaptations of the immune system and innate defense mechanisms against infection. These changes are a consequence of tissue hypoxia per se or can be mediated by hypoxia induced activation of sympathoadrenal pathways. An example of important research activities in recent years is the discovery of hypoxia-inducible factor 1 alpha (HIF1α) and its role in oxygen homoeostasis by regulation of multiple gene loci. Additionally, as a result of hypoxia induced increase in oxidative/reductive stress, enhanced generation of reactive oxygen (ROS) and nitrogen species (RNS), altered activity of antioxidant systems, and related oxidative damage to lipids, proteins, and DNA can occur as well as injury at the cellular, sub-cellular and molecular levels. These short-lived intermediates include among others superoxide anion (O2), hydrogen peroxide (H2O2), and hypochloride (HOCI. In addition, hydroxyl radicals (OH), hydroxide ions (OH) and superoxide radicals (O2-) are highly reactive members of the ROS family that accumulate under certain physiological and pathophysiological conditions. As a consequence, prolonged hypobaric hypoxia leads to systemic oxidative stress similar to severe inflammation.

Tissue hypoxia and increased oxidative stress as well as adaptive or reactive changes in sympathoadrenal and neuroendocrine processes also occur in various disease states. Hypoxia per se plays an important role in the pathogenesis of major causes of mortality, including cancer, cerebral and myocardial ischemia, and chronic heart and lung disease. Global hypoxemia is a common problem in critically ill patients: In patients with pulmonary failure profound hypoxia can occur due to ventilation/perfusion mismatch or impaired diffusion capacity across the alveolo-capillary membrane despite best medical support including mechanical ventilation. Oxygen delivery to tissues might also be impaired due to low cardiac output or reduced oxygen carrying capacity in anemia. Microcirculatory dysfunction - occurring in the context of severe sepsis - can lead to local hypoxia on a cellular level even in patients with normal or increased arterial oxygen content and oxygen delivery.

In critically ill patients cellular hypoxia induces oxidative stress which can deplete cellular antioxidative capacities and lead to impaired ability to use available oxygen. Depleted levels of reduced glutathione, an important intra-mitochondrial antioxidant, in combination with increased generation of ROS and RNS seem to inhibit oxidative phosphorylation and ATP generation. There is increasing interest in ROS-intermediates and their role in the progression and modulation of vascular dysfunction and remodelling seen in different chronic disease entities, such as diabetes mellitus, chronic heart failure or chronic obstructive pulmonary disease (COPD) and development of pulmonary hypertension (PHT). The mechanisms of ROS-generation are not fully understood. ROS are produced in leukocytes, but the generation of ROS might also occur through disruption of the electron transport chain in mitochondria. The resulting mitochondrial dysfunction has been described as an additional factor causing pulmonary vasoconstriction and remodelling in PHT. In hypoxic patients with respiratory failure an increase of pulmonary vascular pressure frequently occurs (WHO Class III - pulmonary hypertension) which may worsen hypoxemia by impairing lung perfusion. If this increase is caused by a direct vasoconstrictive effect of hypoxia on the pulmonary endothelial cells or by an increase in ROS is still not fully understood.

Generally, the mechanisms leading to adaptation to prolonged hypoxic conditions in healthy humans and in critically ill patients are not well understood. In the context of critical illness these mechanisms are difficult to explore due to the heterogeneity of patients and precipitating illnesses. Furthermore, effects of hypoxia and concurring disease related processes are difficult or impossible to distinguish. Animal models of critical illness might have substantial limitations and often do not represent the human patient. It has been suggested that the physiological and pathophysiological responses to hypobaric hypoxia may be similar to responses seen in critical illness. In the context of a high altitude expedition human subjects can safely be submitted to prolonged hypoxia and oxidative stress and the resulting cerebral, cardiovascular and pulmonary adaptation and changes in mitochondrial function, inflammatory cascade, and coagulatory activity can be explored in a controlled fashion. The study of human responses to hypoxia occurring in a hypobaric environment in healthy volunteers ascending to high altitudes may therefore serve as a model of isolated hypoxia and might help to improve our understanding of the effects in critically ill patients.

Objective

The aim of the project "High Altitude Medical Research Expedition Himlung 2013" (HiReach2013) is to comprehensively investigate the cerebral, cardiovascular and pulmonary adaptation and the reactions of the human coagulation system during an ascent to extreme altitudes of over 7000 m.

Methods

Cardiopulmonary exercise testing will be done using a testing system on a bicycle using a roller trainer for standardization and regulation of the work load. Static and dynamic lung volumes will be assessed at each study site. The measurements will include the assessment DLCO using a commercially available spirometer. Transthoracic Doppler echocardiography will be performed for assessment of systolic/diastolic cardiac function and pulmonary artery pressures. Lung ultrasound will be applied in each subject at each study site to quantify extravascular lung water by ultrasound lung comets. Microparticle measurements will be performed using an Annexin V based ELISA. Cerebral blood flow velocity will be measured from a middle cerebral artery using transcranial Doppler. Structural cerebral changes and cerebral volume will be assessed with MRI of the brain. At each study site extensive coagulation studies will be performed.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: June 2013
• Est. primary completion date: June 2013
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Subjects must be healthy, well trained and have basic mountaineering experience

• Written informed consent

Exclusion Criteria

• Subjects with any type of cardiac and or respiratory disease

• Subjects with diabetes mellitus type I or II

• Regular intake of beta-blockers, ACE-inhibitors, nitrates and calcium antagonists as well as corticosteroids or anti-inflammatory medication

• Subjects who developed high altitude pulmonary edema after a rapid ascent (< 3 nights) at altitudes below 3500m

• Subjects who developed severe acute mountain sickness and/or high altitude cerebral edema after rapid ascent to altitudes below 3500m

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Hypoxia

Intervention

Other:
• Hypobaric hypoxia
Subjects are exposed to hypobaric hypoxia in the context of a high altitude expedition.

Locations

Country	Name	City	State
Switzerland	Departement of Intensive Care Medicine	Bern

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital Inselspital, Berne

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pulmonary adaption to hypoxia		Time of reaching 4 different altitudes, expected to be after 1 month	No
Secondary	Cerebral adaption to hypoxia		Time of reaching 4 different altitudes, expected to be after 1 month	No
Secondary	Cardiovascular adaption to hypoxia		Time of reaching 4 different altitudes, expected to be after 1 month	No
Secondary	Adaption of the coagulation system		Time of reaching 4 different altitudes, expected to be after 1 month	No