HypoADAPT: Metabolic Adaptation to High-frequent Hypoglycaemia in Type 1 Diabetes
Study Details
Study Description
Brief Summary
An experimental observational case-control study. The overall objective is to gain new knowledge about mechanisms involved in adaptation to recurrent hypoglycaemia in diabetes by investigating patients with type 1 diabetes and healthy controls. The knowledge to be obtained may feed into experimental hypoglycaemic clamp studies to further elucidate the effect of the adaptations during acute hypoglycaemia. Ultimately, it may lead to intervention studies aiming at the maintenance of functional capability during hypoglycaemia in patients with type 1 diabetes to reduce their risk of severe hypoglycaemia.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Study rationale The risk of severe hypoglycaemia is a major daily concern for people with diabetes treated with insulin. Severe hypoglycaemia is the main barrier in achieving the recommended glycaemic targets and may indirectly be the main driver for late diabetic complications and related morbidity, mortality and health care costs. In people with diabetes, recurrent exposure to insulin-induced mild hypoglycaemia leads to significant adaptive physiologic responses. While the metabolism of the brain and hormonal responses to hypoglycaemia have been studied extensively, this study will as the first, systematically investigate the chronic adaptation of peripheral metabolism to recurrent hypoglycaemia in diabetes. Knowledge about such responses can lead to interventions that attenuate the devastating effects of acute hypoglycaemia induced by insulin in people with diabetes. Thereby, the risk of developing severe hypoglycaemia can be reduced which ultimately will improve long-term diabetes outcomes and reduce health care costs.
Hypothesis Patients with type 1 diabetes that are exposed to high-frequent recurrent hypoglycaemia will adapt their metabolism in a way, which supports the preservation of brain fuelling.
Objectives
Primary objective The overall objective is to gain new knowledge about mechanisms involved in adaptation to recurrent hypoglycaemia in diabetes by investigating patients with type 1 diabetes and healthy controls. The knowledge to be obtained may feed into experimental hypoglycaemic clamp studies to further elucidate the effect of the adaptations during acute hypoglycaemia. Ultimately, it can lead to intervention studies aiming at the maintenance of functional capability during hypoglycaemia in patients with type 1 diabetes to reduce their risk of severe hypoglycaemia.
Secondary objectives
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To study the metabolic consequences of recurrent hypoglycaemia in the brain, liver, muscle and adipose tissues
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To study the consequences of recurrent hypoglycaemia on resting metabolic rest
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To study the consequences of recurrent hypoglycaemia on glucagon and adrenaline sensitivity
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To study the consequences of recurrent hypoglycaemia on epigenetic profiles
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To study the consequences of recurrent hypoglycaemia on oxidative stress
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To study the psychological factors associated with recurrent hypoglycaemia
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: T1DM with frequent hypoglycaemia Participants with CGM-confirmed frequent hypoglycemia prior to inclusion. |
Drug: insulin human
Hyperinsulinemic glucose clamp studies require that insulin is administered at a steady continuous rate to achieve stable levels of hyperinsulinemia. To reach this, insulin needs to be infused intravenously using a standard intravenous pump system. The insulin dose will be adjusted according to the body surface area, aiming for insulin levels of ~170 mU/l, which is within the physiological range. Thus, for a subject with a bodyweight of 70 kg, body length of 180 cm and - consequently - a body surface area of 1.936 m2, the required insulin infusion can be calculated as: 1.936 x 60 x 60 ÷ 1000 = 7.0 units per hour
Other Names:
Drug: Epinephrin
Epinephrine are prepared in 100 ml isotone saline solution according to weight and infused in 3 different infusion rates: 10 ng∙kg-1∙min-1, 25 ng∙kg-1∙min-1 and 50 ng∙kg-1∙min-1, for 20 minutes each. After each adrenaline infusion, substrate response will be measured by blood samples of glucose, lactate, free fatty acids, alanine, β-hydroxybutyrate, glycerol and insulin. Furthermore, cardiovascular measurements such as pulse and blood pressure are monitored as well.
Other Names:
Procedure: Muscle biopsy
With the study subject resting in the supine position, the skin is disinfected on the lateral side of the thigh around 15 cm above the knee, with chlorhexidine alcohol. Then 3-4 mL of local anaesthetic (lidocaine 20 mg/mL) is injected into the skin, subcutaneous tissue and in the upper part of the muscle with a very thin needle. When the anaesthetic effect has set in after a couple of minutes an insertion is made in the skin and the subcutaneous tissue through which the biopsy cannula is inserted into the muscle. A small piece (around 150 mg) of the muscle is collected, which may be experienced as somewhat unpleasant, but will last for a very short while ( ~1-2 seconds). The needle is removed, a sterile Band-Aid is applied, and the study subject can leave the site after termination of the trial. The biopsy may cause some muscular tenderness for 2-3 days corresponding to minor muscular trauma.
Procedure: Adipose tissue biopsy
With the study subject resting in the supine position, the skin is disinfected on one side of the abdomen around 5-10 cm lateral from the umbilicus to the knee, with chlorhexidine alcohol. Then 3-4 mL of local anaesthetic (lidocaine 20 mg/mL) is injected into the skin, subcutaneous tissue and in the upper part of the adipose tissue with a very thin needle. When the anaesthetic effect has set in after a couple of minutes an insertion is made in the skin and the subcutaneous tissue through which the biopsy cannula is inserted into the adipose tissue. A small piece (around 1 gram) of the adipose tissue is collected, which may be experienced as somewhat unpleasant, but will last for a very short while ( ~1-2 seconds). The needle is removed, a sterile Band-Aid is applied, and the study subject can leave the site after termination of the trial. The biopsy may cause some tenderness for 2-3 days corresponding to minor trauma.
Drug: Glucagon
Glucagon is prepared in doses of 10 µg, 25 µg, and 50 µg and intravenously injected with intervals of 2 hours. After each glucagon injection, blood samples will be drawn to measure plasma glucose, glucagon, lactate, free fatty acids, alanine, amino-acids, β-hydroxybutyrate, glycerol and insulin. Furthermore, cardiovascular measurements such as pulse and blood pressure are monitored as well.
Other Names:
Device: IPRO 2 Medtronic Minimed
All potential subjects will receive a blinded continuous glucose sensor at Visit 1. At the following visits, the CGM will be reviewed for hypoglycaemia episodes and replaced at the same time. At Visit 2 a final screening of the inclusion criteria will take place, which involves the CGM data of the first week. A blinded CGM will be installed a week before every visit.
Other Names:
Procedure: 7T Magnetic Resonance Imaging
Subjects will undergo a hyperinsulinemic euglycaemic glucose clamp, as mentioned above, in the MRI scanning room. After 30 minutes of stable normoglycaemia, subjects are taken into the MRI scanner (Philips Achieva 7.0 T) where brain, liver, thigh and calf muscle are scanned. After every anatomically different area, the subjects must be taken out of the scanner, while scanning coils are replaced. All subjects are advised to lie still and press the alarm button if necessary.
Other Names:
Procedure: Indirect Caliometry using Jaeger Oxycon Champion
Resting metabolic rate will be estimated, after reaching stable plasma glucose level, via a hyperinsulinemic euglycaemic clamp, as mentioned above. This will be done by indirect calorimetry, using a ventilated hood system (Jaeger Oxycon Champion, software version 4.3, Jaeger, Mijnhardt). Subjects are instructed to lie down and rest for a period of 30 minutes. Subjects are also instructed not to move, talk or sleep unless necessary during the period of measurement. The recorded measurement after 5 minutes to 30 minutes will be used for analysis.
Procedure: Core temperature and thermography using Thermovision SC645
Thermography (Thermovision SC645, FLIR Systems, Wilsonville, OR, USA) is used to determine cutaneous vascular perfusion. Data is analogue-digital converted and sampled at 100 Hz (Powerlab, ADInstruments, Colorado Springs, CO, USA).
|
| Active Comparator: T1DM with no hypoglycaemia Participants with no CGM-confirmed hypoglycemia prior to inclusion. |
Drug: insulin human
Hyperinsulinemic glucose clamp studies require that insulin is administered at a steady continuous rate to achieve stable levels of hyperinsulinemia. To reach this, insulin needs to be infused intravenously using a standard intravenous pump system. The insulin dose will be adjusted according to the body surface area, aiming for insulin levels of ~170 mU/l, which is within the physiological range. Thus, for a subject with a bodyweight of 70 kg, body length of 180 cm and - consequently - a body surface area of 1.936 m2, the required insulin infusion can be calculated as: 1.936 x 60 x 60 ÷ 1000 = 7.0 units per hour
Other Names:
Drug: Epinephrin
Epinephrine are prepared in 100 ml isotone saline solution according to weight and infused in 3 different infusion rates: 10 ng∙kg-1∙min-1, 25 ng∙kg-1∙min-1 and 50 ng∙kg-1∙min-1, for 20 minutes each. After each adrenaline infusion, substrate response will be measured by blood samples of glucose, lactate, free fatty acids, alanine, β-hydroxybutyrate, glycerol and insulin. Furthermore, cardiovascular measurements such as pulse and blood pressure are monitored as well.
Other Names:
Procedure: Muscle biopsy
With the study subject resting in the supine position, the skin is disinfected on the lateral side of the thigh around 15 cm above the knee, with chlorhexidine alcohol. Then 3-4 mL of local anaesthetic (lidocaine 20 mg/mL) is injected into the skin, subcutaneous tissue and in the upper part of the muscle with a very thin needle. When the anaesthetic effect has set in after a couple of minutes an insertion is made in the skin and the subcutaneous tissue through which the biopsy cannula is inserted into the muscle. A small piece (around 150 mg) of the muscle is collected, which may be experienced as somewhat unpleasant, but will last for a very short while ( ~1-2 seconds). The needle is removed, a sterile Band-Aid is applied, and the study subject can leave the site after termination of the trial. The biopsy may cause some muscular tenderness for 2-3 days corresponding to minor muscular trauma.
Procedure: Adipose tissue biopsy
With the study subject resting in the supine position, the skin is disinfected on one side of the abdomen around 5-10 cm lateral from the umbilicus to the knee, with chlorhexidine alcohol. Then 3-4 mL of local anaesthetic (lidocaine 20 mg/mL) is injected into the skin, subcutaneous tissue and in the upper part of the adipose tissue with a very thin needle. When the anaesthetic effect has set in after a couple of minutes an insertion is made in the skin and the subcutaneous tissue through which the biopsy cannula is inserted into the adipose tissue. A small piece (around 1 gram) of the adipose tissue is collected, which may be experienced as somewhat unpleasant, but will last for a very short while ( ~1-2 seconds). The needle is removed, a sterile Band-Aid is applied, and the study subject can leave the site after termination of the trial. The biopsy may cause some tenderness for 2-3 days corresponding to minor trauma.
Drug: Glucagon
Glucagon is prepared in doses of 10 µg, 25 µg, and 50 µg and intravenously injected with intervals of 2 hours. After each glucagon injection, blood samples will be drawn to measure plasma glucose, glucagon, lactate, free fatty acids, alanine, amino-acids, β-hydroxybutyrate, glycerol and insulin. Furthermore, cardiovascular measurements such as pulse and blood pressure are monitored as well.
Other Names:
Device: IPRO 2 Medtronic Minimed
All potential subjects will receive a blinded continuous glucose sensor at Visit 1. At the following visits, the CGM will be reviewed for hypoglycaemia episodes and replaced at the same time. At Visit 2 a final screening of the inclusion criteria will take place, which involves the CGM data of the first week. A blinded CGM will be installed a week before every visit.
Other Names:
Procedure: 7T Magnetic Resonance Imaging
Subjects will undergo a hyperinsulinemic euglycaemic glucose clamp, as mentioned above, in the MRI scanning room. After 30 minutes of stable normoglycaemia, subjects are taken into the MRI scanner (Philips Achieva 7.0 T) where brain, liver, thigh and calf muscle are scanned. After every anatomically different area, the subjects must be taken out of the scanner, while scanning coils are replaced. All subjects are advised to lie still and press the alarm button if necessary.
Other Names:
Procedure: Indirect Caliometry using Jaeger Oxycon Champion
Resting metabolic rate will be estimated, after reaching stable plasma glucose level, via a hyperinsulinemic euglycaemic clamp, as mentioned above. This will be done by indirect calorimetry, using a ventilated hood system (Jaeger Oxycon Champion, software version 4.3, Jaeger, Mijnhardt). Subjects are instructed to lie down and rest for a period of 30 minutes. Subjects are also instructed not to move, talk or sleep unless necessary during the period of measurement. The recorded measurement after 5 minutes to 30 minutes will be used for analysis.
Procedure: Core temperature and thermography using Thermovision SC645
Thermography (Thermovision SC645, FLIR Systems, Wilsonville, OR, USA) is used to determine cutaneous vascular perfusion. Data is analogue-digital converted and sampled at 100 Hz (Powerlab, ADInstruments, Colorado Springs, CO, USA).
|
| Active Comparator: Healthy Controls Healthy Controls |
Drug: insulin human
Hyperinsulinemic glucose clamp studies require that insulin is administered at a steady continuous rate to achieve stable levels of hyperinsulinemia. To reach this, insulin needs to be infused intravenously using a standard intravenous pump system. The insulin dose will be adjusted according to the body surface area, aiming for insulin levels of ~170 mU/l, which is within the physiological range. Thus, for a subject with a bodyweight of 70 kg, body length of 180 cm and - consequently - a body surface area of 1.936 m2, the required insulin infusion can be calculated as: 1.936 x 60 x 60 ÷ 1000 = 7.0 units per hour
Other Names:
Drug: Epinephrin
Epinephrine are prepared in 100 ml isotone saline solution according to weight and infused in 3 different infusion rates: 10 ng∙kg-1∙min-1, 25 ng∙kg-1∙min-1 and 50 ng∙kg-1∙min-1, for 20 minutes each. After each adrenaline infusion, substrate response will be measured by blood samples of glucose, lactate, free fatty acids, alanine, β-hydroxybutyrate, glycerol and insulin. Furthermore, cardiovascular measurements such as pulse and blood pressure are monitored as well.
Other Names:
Procedure: Muscle biopsy
With the study subject resting in the supine position, the skin is disinfected on the lateral side of the thigh around 15 cm above the knee, with chlorhexidine alcohol. Then 3-4 mL of local anaesthetic (lidocaine 20 mg/mL) is injected into the skin, subcutaneous tissue and in the upper part of the muscle with a very thin needle. When the anaesthetic effect has set in after a couple of minutes an insertion is made in the skin and the subcutaneous tissue through which the biopsy cannula is inserted into the muscle. A small piece (around 150 mg) of the muscle is collected, which may be experienced as somewhat unpleasant, but will last for a very short while ( ~1-2 seconds). The needle is removed, a sterile Band-Aid is applied, and the study subject can leave the site after termination of the trial. The biopsy may cause some muscular tenderness for 2-3 days corresponding to minor muscular trauma.
Procedure: Adipose tissue biopsy
With the study subject resting in the supine position, the skin is disinfected on one side of the abdomen around 5-10 cm lateral from the umbilicus to the knee, with chlorhexidine alcohol. Then 3-4 mL of local anaesthetic (lidocaine 20 mg/mL) is injected into the skin, subcutaneous tissue and in the upper part of the adipose tissue with a very thin needle. When the anaesthetic effect has set in after a couple of minutes an insertion is made in the skin and the subcutaneous tissue through which the biopsy cannula is inserted into the adipose tissue. A small piece (around 1 gram) of the adipose tissue is collected, which may be experienced as somewhat unpleasant, but will last for a very short while ( ~1-2 seconds). The needle is removed, a sterile Band-Aid is applied, and the study subject can leave the site after termination of the trial. The biopsy may cause some tenderness for 2-3 days corresponding to minor trauma.
Drug: Glucagon
Glucagon is prepared in doses of 10 µg, 25 µg, and 50 µg and intravenously injected with intervals of 2 hours. After each glucagon injection, blood samples will be drawn to measure plasma glucose, glucagon, lactate, free fatty acids, alanine, amino-acids, β-hydroxybutyrate, glycerol and insulin. Furthermore, cardiovascular measurements such as pulse and blood pressure are monitored as well.
Other Names:
Device: IPRO 2 Medtronic Minimed
All potential subjects will receive a blinded continuous glucose sensor at Visit 1. At the following visits, the CGM will be reviewed for hypoglycaemia episodes and replaced at the same time. At Visit 2 a final screening of the inclusion criteria will take place, which involves the CGM data of the first week. A blinded CGM will be installed a week before every visit.
Other Names:
Procedure: 7T Magnetic Resonance Imaging
Subjects will undergo a hyperinsulinemic euglycaemic glucose clamp, as mentioned above, in the MRI scanning room. After 30 minutes of stable normoglycaemia, subjects are taken into the MRI scanner (Philips Achieva 7.0 T) where brain, liver, thigh and calf muscle are scanned. After every anatomically different area, the subjects must be taken out of the scanner, while scanning coils are replaced. All subjects are advised to lie still and press the alarm button if necessary.
Other Names:
Procedure: Indirect Caliometry using Jaeger Oxycon Champion
Resting metabolic rate will be estimated, after reaching stable plasma glucose level, via a hyperinsulinemic euglycaemic clamp, as mentioned above. This will be done by indirect calorimetry, using a ventilated hood system (Jaeger Oxycon Champion, software version 4.3, Jaeger, Mijnhardt). Subjects are instructed to lie down and rest for a period of 30 minutes. Subjects are also instructed not to move, talk or sleep unless necessary during the period of measurement. The recorded measurement after 5 minutes to 30 minutes will be used for analysis.
Procedure: Core temperature and thermography using Thermovision SC645
Thermography (Thermovision SC645, FLIR Systems, Wilsonville, OR, USA) is used to determine cutaneous vascular perfusion. Data is analogue-digital converted and sampled at 100 Hz (Powerlab, ADInstruments, Colorado Springs, CO, USA).
|
Outcome Measures
Primary Outcome Measures
- Metabolite- and lipid profiling [5 minutes]
Metabolite- and lipid profiling of blood samples using metabolomics profiling platforms during euglycaemia
- Brain lactacte concentration [20 minutes]
Brain lactacte concentration using non-invasive MR spectroscopy during euglycaemia
- Brain ATP concentration [20 minutes]
Brain ATP concentration using non-invasive MR spectroscopy during euglycaemia
- Glycogen in muscle and adipose tissue [5 minutes]
Glycogen in muscle and adipose tissue biopsies during euglycaemia
- Non-specific proteins in muscle and adipose tissue [5 minutes]
Non-specific proteins in muscle and adipose tissue biopsies during euglycaemia
- Glycogen concentration [40 minutes]
Glycogen in liver and muscle tissue using non-invasive MR spectroscopy during euglycaemia.
Secondary Outcome Measures
- Estimated glucose production during glucagon stimulation [Every 5 minutes up to 5 hours]
Area under the aggregation curve (AUC) for plasma glucose during glucagon injections. Plasma glucose measurement
- Estimated glucose production during epinephrine stimulation [Every 5 minutes up to 90 minutes]
Area under the aggregation curve (AUC) for plasma glucose during epinephrine infusion. Plasma glucose measurement
- Indirect calorimetri [60 minutes]
Estimating resting metabolic rate, before and during hyperinsulinemic-hypoglycemic clamp
- Thermography [5 minutes]
Estimating skin temperature, before and during hyperinsulinemic-hypoglycemic clamp
- Plasma lactate during glucagon injections. [Every 40 minutes up to 5 hours]
Plasma lactate during glucagon injections.
- Plasma free fatty acids during glucagon injections. [Every 40 minutes up to 5 hours]
Plasma free fatty acids during glucagon injections.
- Plasma glycerol during glucagon injections. [Every 40 minutes up to 5 hours]
Plasma glycerol during glucagon injections.
- Plasma alanine during glucagon injections. [Every 40 minutes up to 5 hours]
Plasma alanine during glucagon injections.
- Plasma beta-hydroxybutyurate during glucagon injections. [Every 40 minutes up to 5 hours]
Plasma beta-hydroxybutyurate during glucagon injections.
- Plasma insulin during glucagon injections. [Every 40 minutes up to 5 hours]
Plasma insulin during glucagon injections.
- Plasma glucagon during glucagon injections. [Every 40 minutes up to 5 hours]
Plasma glucagon during glucagon injections.
- Plasma metabolomics during glucagon injections. [Every 40 minutes up to 5 hours]
Plasma metabolomics during glucagon injections.
- Plasma lactate during epinephrine infusion [Every 20 minutes up to 90 minutes]
Plasma lactate during epinephrine infusion
- Plasma free fatty acids during epinephrine infusion [Every 20 minutes up to 90 minutes]
Plasma free fatty acids during epinephrine infusion
- Plasma glycerol during epinephrine infusion [Every 20 minutes up to 90 minutes]
Plasma glycerol during epinephrine infusion
- Plasma alanine during epinephrine infusion [Every 20 minutes up to 90 minutes]
Plasma alanine during epinephrine infusion
- Plasma beta-hydroxybutyurate during epinephrine infusion [Every 20 minutes up to 90 minutes]
Plasma beta-hydroxybutyurate during epinephrine infusion
- Plasma insulin during epinephrine infusion [Every 20 minutes up to 90 minutes]
Plasma insulin during epinephrine infusion
- Plasma glucagon during epinephrine infusion [Every 20 minutes up to 90 minutes]
Plasma glucagon during epinephrine infusion
- Plasma catecholamines during epinephrine infusion [Every 20 minutes up to 90 minutes]
Plasma catecholamines during epinephrine infusion
- Plasma metabolomics during epinephrine infusion [Every 20 minutes up to 90 minutes]
Plasma metabolomics during epinephrine infusion
- Biochemical analyses [5 minutes]
Plasma Samples to analyze Cortisol, Growth Hormone, Insulin-like growth factor, Catecholamines, Lactate, Free Fatty Acids, Glycerol, Alanine, Beta-hydroxybutyurate, Insulin, Glucagon, Catecholamines and erythropoietin. Before and during hyperinsulinemic-hypoglycemic clamp.
- Personality traits using the psychometry questionnaire DS-14 [30 minutes]
Personality traits using the psychometry questionnaire DS-14
- Personality traits using the psychometry questionnaire TAS-20 [30 minutes]
Personality traits using the psychometry questionnaire TAS-20
- Diabetes and hypoglycaemia status using psychometry questionnaire HFS-W [30 minutes]
Diabetes and hypoglycaemia status using psychometry questionnaire HFS-W
- Diabetes and hypoglycaemia status using psychometry questionnaire HABS [30 minutes]
Diabetes and hypoglycaemia status using psychometry questionnaire HABS
- Diabetes and hypoglycaemia status using psychometry questionnaire PAID [30 minutes]
Diabetes and hypoglycaemia status using psychometry questionnaire PAID
- Food consumption [30 minutes]
Using Food Frequency Questionnaire to analyze food consumption
- Hypoglycemia awareness status [10 minutes]
Using hypoglycemia awareness status questionnaire
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Ability to provide written informed consent
-
Male or female aged 18-70 years
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Must be able to speak and read Danish
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Type 1 diabetes patients with HbA1c <48 mmol/mol (Case A) or >70 mmol/mol (Case B)
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CGM-documented frequent exposure to hypoglycaemia (Case A) or CGM without hypoglycaemia (Case B) for 6 days.
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A documented clinically relevant history of type 1 diabetes
-
In insulin treatment regimen
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The subject must be willing and able to comply with trial protocol
Exclusion Criteria:
-
History of severe psychological condition
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History of severe heart disease
-
History of epilepsy, former apoplexies and dementia
-
History of muscle diseases
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History of liver disease
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History of malignancy unless a disease-free period exceeding 5 years
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Implants not compatible for MRI scans
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History of alcohol or drug abuse
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Pregnant or lactating woman
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Steno Diabetes Center Copenhagen | Gentofte | Denmark | 2820 | |
| 2 | Nordsjaellands Hospital | Hillerød | Denmark | 3400 |
Sponsors and Collaborators
- Nordsjaellands Hospital
- Danish Research Centre for Magnetic Resonance
- University of Copenhagen
- Steno Diabetes Center Copenhagen
Investigators
- Principal Investigator: Ulrik Pedersen-Bjergaard, MD,PhD,Prof, Nordsjaellands Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- DRCMR7T-06
- 2019-001938-34