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N/A N=10 Randomized Basic Science

High Altitude and Exogenous Carbohydrate Oxidation

Glucose Metabolism · High Altitude

Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Sep 2021
Primary outcome: Primary: Rate of Exogenous Carbohydrate Oxidation — 0.44; 0.35 g/min

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Sea Level (Other); High Altitude (Other)
Age
Adult · 18+ yrs
Sex
Male
Sponsor
United States Army Research Institute of Environmental Medicine
Primary completion
Nov 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Rate of Exogenous Carbohydrate Oxidation
0.44; 0.35
PRIMARY
Rate of Glucose Turnover
14.3; 12.7; 12.1; 8.9

Summary

Recent studies have reported that oxidation of exogenous carbohydrate is reduced under acute hypobaric hypoxic (high altitude; HA) conditions compared to normoxia (sea level; SL) in native lowlanders. However, the mechanisms by which HA suppresses exogenous carbohydrate oxidation are not known. This study will seek to confirm that acute HA exposure decreases exogenous carbohydrate oxidation during steady-state aerobic exercise compared to SL, and explore if the mechanism inhibiting plasma glucose uptake is insulin dependent or independent.

Eligibility Criteria

Inclusion Criteria

  • Men aged 18 - 39 years
  • Born at altitudes less than 2, 100 m (~7,000 feet; Examples include Santa Fe, New Mexico; Laramie, Wyoming; Etc.)
  • Physically active based on assessment of physical activity history (2-4 days per week aerobic and/or resistance exercise)
  • Have supervisor approval (permanent party military and civilians)
  • Willing to refrain from alcohol, smokeless nicotine products and dietary supplement use during study periods
  • Refrain from taking any nonsteroidal anti-inflammatory drugs (NSAIDs; e.g. aspirin, Advil®, Aleve®, Naprosyn®, or any aspirin-containing product) for 10 days before and at least 5 days AFTER each muscle biopsy. (*Tylenol® or acetaminophen is ok to use if needed for discomfort)

Exclusion Criteria

  • Born at altitudes greater than 2, 100 m (~7,000 feet; Examples include Santa Fe, New Mexico; Laramie, Wyoming; Etc.)
  • Living in areas that are more than 1,200 m (~4,000 feet), or have traveled to areas that are more than 1,200 m for five days or more within the last 2 months (Examples include Ft. Huachuca, Arizona; Lima, Peru; Feldberg, Germany, Etc.)
  • Musculoskeletal injuries that compromise exercise capability
  • Metabolic or cardiovascular abnormalities (determined by resting ECG), gastrointestinal disorders (e.g., kidney disease, diabetes, cardiovascular disease, etc.)
  • Medication that affects macronutrient metabolism (i.e., diabetes medications, statins, corticosteroids, etc) and/or the ability to participate in strenuous exercise
  • Evidence of apnea or other sleeping disorders
  • Prior diagnosis of high altitude pulmonary edema (HAPE) or high altitude cerebral edema (HACE)
  • Presence of asthma or respiratory tract infections (< 1 month prior)
  • Allergies or intolerance to foods (including but not limited to lactose intolerance/milk allergy), vegetarian practices, or medications (including, but not limited to, lidocaine ) to be utilized in the study
  • Smoking or vaping
  • History of complications with lidocaine
  • Taking medications that interfere with oxygen delivery and transport (Includes sedatives, sleeping aids, tranquilizers and/or any medication that depresses ventilation, diuretics, alpha and beta blockers)
  • Evidence of any physical, mental, and/or medical conditions that would make the proposed studies relatively more hazardous as determined by the Office of Medical Support and Oversight
  • Present condition of alcoholism, anabolic steroids, or other substance abuse issues
  • Anemia (hematocrit <38% and hemoglobin <12.5 g/dL) and Sickle Cell Anemia/Trait
  • Abnormal prothrombin time (PT)/ partial thromboplastin time (PTT) test or problems with blood clotting
  • Blood donation within 8 weeks of beginning the study
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03851744). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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