Measurement of Glucose/Glycogen Metabolism in Humans Using Magnetic Resonance at 4 or 7 Tesla
Status: | Completed |
---|---|
Conditions: | Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 18 - 65 |
Updated: | 1/20/2018 |
Start Date: | December 2004 |
End Date: | December 2017 |
The long-range goal of this project is to determine the effects of diabetes and the
hypoglycemic consequences of intensive therapy on in vivo brain glucose metabolism in humans.
We will measure brain glycogen turnover and content in normal controls and subjects with
diabetes under conditions of modest hyper-and hypoglycemia.
hypoglycemic consequences of intensive therapy on in vivo brain glucose metabolism in humans.
We will measure brain glycogen turnover and content in normal controls and subjects with
diabetes under conditions of modest hyper-and hypoglycemia.
On the morning before the study subjects will report to the Clinical Research Center and will
be asked to stay at the Clinical Research Center for up to 72 hours. You will be asked not to
eat anything after midnight. Small plastic catheters will be placed in two veins in subjects
arms for infusion of glucose and for measuring blood glucose levels every 15-30 minutes.
While subjects are in the study they will continuously receive a small dose of glucose
enriched with 13C label either through the catheter or by drinking a small amount of a sugar
water solution every 15-60 minutes. Subjects will be asked to transfer to the Center for
Magnetic Resonance Research every 6-8 hours (except at night) where they will be asked each
time to conduct an MRI scan as follows: Subjects will be placed on the patient bed in the
magnet room for one-to-two hours. A nurse will stay with the subject at all times during this
study. During some of the scans subjects may be asked to perform a visual task such as
watching a changing checkerboard pattern through a mirror placed in front of their eyes.
After each scan subjects will receive a low carbohydrate meal for weight-maintenance.
Subjects may be asked to receive an infusion of glucose and/or insulin one-to-three times
before and/or after the infusion of 13C-enriched glucose starts. During these infusions the
subject's blood sugar will be maintained either higher or lower than normal levels for up to
3 hours. This will be done to assess the effect of hyper- or hypoglycemia on brain glycogen
metabolism.
Subjects may also be asked several days prior to the study to report to the Clinical Research
Center for a "mock" study to see if they are comfortable with the MRI scan and/or to test
their body's response to either protocol (as described above, but carried out at the Clinical
Research Center). If subjects would like to try the MRI procedure in advance, this test will
not exceed 2 hours. If we need to test the subject's response to the infusion, this
"pre-test" will involve only drawing blood and administering glucose and will be performed as
described for either protocol above, but will last not more than 4 hours.
Magnetic resonance measurements will be performed in the magnet and are very similar to
magnetic resonance imaging exams (MRI). Subjects will always have the possibility to signal
when they feel claustrophobic and wish to be removed from the magnet. The magnetic resonance
measurements will be associated with a regular clunking noise that subjects may initially
find unpleasant. For their comfort they will be offered to wear ear plugs. During the
measurements in the magnet subjects will be asked to lie still for most of the time.
be asked to stay at the Clinical Research Center for up to 72 hours. You will be asked not to
eat anything after midnight. Small plastic catheters will be placed in two veins in subjects
arms for infusion of glucose and for measuring blood glucose levels every 15-30 minutes.
While subjects are in the study they will continuously receive a small dose of glucose
enriched with 13C label either through the catheter or by drinking a small amount of a sugar
water solution every 15-60 minutes. Subjects will be asked to transfer to the Center for
Magnetic Resonance Research every 6-8 hours (except at night) where they will be asked each
time to conduct an MRI scan as follows: Subjects will be placed on the patient bed in the
magnet room for one-to-two hours. A nurse will stay with the subject at all times during this
study. During some of the scans subjects may be asked to perform a visual task such as
watching a changing checkerboard pattern through a mirror placed in front of their eyes.
After each scan subjects will receive a low carbohydrate meal for weight-maintenance.
Subjects may be asked to receive an infusion of glucose and/or insulin one-to-three times
before and/or after the infusion of 13C-enriched glucose starts. During these infusions the
subject's blood sugar will be maintained either higher or lower than normal levels for up to
3 hours. This will be done to assess the effect of hyper- or hypoglycemia on brain glycogen
metabolism.
Subjects may also be asked several days prior to the study to report to the Clinical Research
Center for a "mock" study to see if they are comfortable with the MRI scan and/or to test
their body's response to either protocol (as described above, but carried out at the Clinical
Research Center). If subjects would like to try the MRI procedure in advance, this test will
not exceed 2 hours. If we need to test the subject's response to the infusion, this
"pre-test" will involve only drawing blood and administering glucose and will be performed as
described for either protocol above, but will last not more than 4 hours.
Magnetic resonance measurements will be performed in the magnet and are very similar to
magnetic resonance imaging exams (MRI). Subjects will always have the possibility to signal
when they feel claustrophobic and wish to be removed from the magnet. The magnetic resonance
measurements will be associated with a regular clunking noise that subjects may initially
find unpleasant. For their comfort they will be offered to wear ear plugs. During the
measurements in the magnet subjects will be asked to lie still for most of the time.
Inclusion Criteria:
- Age 18-65
- Healthy control
- Must be able to provide informed consent
- Type 1 diabetes with hypoglycemia unawareness with hemoglobin A1c < 7.5%
- Poorly controlled diabetics with hemoglobin A1c > 7.5%
- Subjects with hypoglycemia unawareness must report an inability to recognize at least
some blood glucose values <58 mg/dL during the 3 months prior to the study.
Exclusion Criteria:
- Over 300 pounds
- Claustrophobic
- History of ischemic heart disease, arrhythmia, of seizure disorder
- Pregnant
- On medications known to alter blood flow or carbohydrate metabolism
- Have internally located pieces of metal
We found this trial at
1
site
Minneapolis, Minnesota 55455
(612) 625-5000
Principal Investigator: Elizabeth R Seaquist, MD
Phone: 612-624-0470
Univ of Minnesota With a flagship campus in the heart of the Twin Cities, and...
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