The Effects of Normobaric Hypoxia on Blood Glucose Levels.



Status:Completed
Conditions:Endocrine
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:18 - Any
Updated:11/23/2013
Start Date:December 2012
End Date:March 2013
Contact:Jill M Teixeira, MBA/HCM, CCRP, CCRC
Email:jill.teixeira@nellis.af.mil
Phone:7026532756

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The purpose of this research study is to observe whether there is a change in blood glucose
levels in response to a 2 hour oral glucose tolerance tests (OGTT) during acute normobaric
hypoxia (short term low oxygen levels at normal ambient air pressure).


A total of 25 subjects (MOFH personnel and DoD beneficiaries) will be recruited from all
male and female subjects whom are at least 18 years of age at the MOFH. All patients who
meet the inclusion criteria will be offered the opportunity to participate by the PI, AI or
study staff. We will recruit patients using the attached Recruitment Flyer and Advertisement
in the Nellis Air Force Base newspaper. All subjects will have at least a one week break in
between each visit and will be told to fast (not eat or drink anything) for at least 8 hours
prior to Visits 1, 2 and 3.. If during the baseline (ground) test any of the 20 non-diabetic
patients are found to be a diabetic, they will be notified and the attached form letter will
be sent to their Primary Care Manager (PCM) alerting them to this finding so that they may
begin treatment. Visit 1, our baseline testing at room air (22% oxygen), is being used as
our control. If the patient exhibits hyperventilation secondary to claustrophobia, the
Principal Investigator or Associate Investigator may disenroll the patient from the study.
No procedures on this research protocol are part of standard of care. They are all done for
research purposes only

Screening Visit:

• The subjects' medical history will be reviewed. Informed Consent and HIPAA Authorization
will be obtained. Females of child bearing potential will then be sent to the laboratory for
a pregnancy test (5-10 milliliters (mls), approximately 1-2 teaspoons of blood). Schedule
patients for Visit 1. Patients will be told to fast for at least 8 hours prior to Visit 1.

Visit 1 (within 1 week of screening visit):

• Subjects will have an intravenous line (IV) inserted in their arm. The subjects will then
be placed on the ROBD2 at room air (22% oxygen) for 2.5 hours. During the altitude
simulation, the subjects will drink a sugar mixture containing 75 grams of sugar for a
2-hour OGTT (glucose levels drawn at 0, 60, 120 minutes) (5-10 milliliters (mls),
approximately 1-2 teaspoons per blood draw), c-peptide tests (drawn at 0, 60, 120 minutes)
(5-10 milliliters (mls), approximately 1-2 teaspoons per blood draw), and will also be asked
to complete the AMS questionnaire (see attached) at 0, 60 and 120 minutes to determine if
they are experiencing any adverse effects of hypoxia. Patients will be told to fast for at
least 8 hours prior to Visit 2.

Visit 2 (at least 1 week after Visit 1):

• The subject will have an intravenous line (IV) inserted in their arm. The subjects will
then be placed on the ROBD2 to produce altitude simulation at 8,000 feet (15.6% oxygen) for
2.5 hours. During the altitude simulation, the subjects will have a 2-hour OGTT (glucose
levels drawn at 0, 60, 120 minutes) (5-10 milliliters (mls), approximately 1-2 teaspoons per
blood draw), c-peptide tests (drawn at 0, 60, 120 minutes) (5-10 milliliters (mls),
approximately 1-2 teaspoons per blood draw), and will also be asked to complete the AMS
questionnaire (see attached) at 0, 60 and 120 minutes to determine if they are experiencing
any adverse effects of hypoxia. Patients will be told to fast for at least 8 hours prior to
Visit 3.

Visit 3 (at least 1 week after Visit 2):

• The subject will have an intravenous line (IV) inserted in their arm. The subjects will
then be placed on the ROBD2 to produce altitude simulation at 12,000 feet (13.4% oxygen) for
2.5 hours. During the altitude simulation, the subjects will have a 2-hour OGTT (glucose
levels drawn at 0, 60, 120 minutes) (5-10 milliliters (mls), approximately 1-2 teaspoons per
blood draw), c-peptide tests (drawn at 0, 60, 120 minutes) (5-10 milliliters (mls),
approximately 1-2 teaspoons per blood draw), and will also be asked to complete the AMS
questionnaire (see attached) at 0, 60 and 120 minutes to determine if they are experiencing
any adverse effects of hypoxia.

Subject's participation in this study will last approximately 3 weeks and is completed after
Visit 3.

If at any time during the study, the subject is found to be diabetic, they will be notified
and referred to their Primary Care Manager (PCM) to initiate standard of care treatment. If
a subject becomes pregnant during the study, they will be withdrawn from the study and
referred to their PCM for standard of care treatment. If patients are withdrawn from the
study, no further testing is required.

Patients must agree to take precautions to prevent pregnancy during the course of this study
due to the possible effects the simulation of altitude may have on an unborn child. The
only completely reliable methods of birth control are total abstinence or surgical removal
of the uterus. Other methods, such as the use of condoms, a diaphragm or cervical cap,
birth control pills, IUD, or sperm killing products are not totally effective in preventing
pregnancy. Also, women who are breastfeeding may not participate in this study.

2-hour OGTT tests are performed to see how quickly glucose is metabolized from the
bloodstream for use by cells as an energy source. This test requires a patient to fast.
Blood is drawn to establish a fasting glucose level. Next, a patient must drink a sugary
beverage (containing a 75 gram glucose load), then blood is drawn again at 60 minutes and
120 minutes after the beverage is consumed.

If during altitude, glucose is elevated, patients will not be removed from the study.

Inclusion Criteria (non-diabetics):

- Tricare Insurance Beneficiary (military insurance) receiving care at Nellis AFB

- 5 males with a BMI < 25; 5 males with a BMI > 25 at least 18 years of age (MOFH
personnel and DoD beneficiaries).

- 5 females with a BMI < 25; 5 females with a BMI > 25 at least 18 years of age (MOFH
personnel and DoD beneficiaries).

Exclusion Criteria (non-diabetics):

- History of abnormal fasting glucose.

- Pulmonary disease.

- Any medications that change glucose control to include systemic steroid and diabetic
medications.

- History of claustrophobia.

- Pregnant or breast feeding.

- Non-English speaking.

- Physical inability to wear/use the ROBD2

Inclusion Criteria (diabetics):

-5 males and/or females, at least 18 years of age, that are type 2 diabetics (MOFH
personnel and DoD beneficiaries).

Exclusion Criteria (diabetics):

- Pulmonary disease.

- History of claustrophobia.

- Pregnant or breast feeding.

- Non-English speaking.

- Physical inability to wear/use the ROBD2
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