Adrenergic System in Islet Transplantation

Early Phase 1

Active, not recruiting

• Conditions: Type1diabetes; Hypoglycemia; Hypoglycemia Unawareness; Islet Cell Transplantation
• Interventions: Drug: Placebo; Drug: Propranolol; Drug: Phentolamine

• Registration Number: NCT03079921
• Lead Sponsor: University of Pennsylvania

Brief Summary

To determine the effect of sympathetic neural and hormonal (epinephrine) input on islet cell hormonal responses to insulin-induced hypoglycemia in type 1 diabetic recipients of intrahepatic islet transplantation. We hypothesize that α-adrenergic (neural) blockage will abolish insulin-mediated suppression of C-peptide, attenuating α-cell glucagon secretion during hypoglycemia, and that β-adrenergic (hormonal) blockage will have no effect. Glucose counterregulatory responses will be measured during hyperinsulinemic euglycemic-hypoglycemic clamps on three occasions with randomized, double-blind administration of the α-adrenergic blocker phentolamine, the β-adrenergic blocker propranolol, or placebo. The demonstration of neural rather than hormonal regulation of the transplanted islet cell response to hypoglycemia is critical for understanding the mechanism for protection from hypoglycemia afforded by intrahepatically transplanted.

Detailed Description

This study is designed to test the hypothesis that α-adrenergic (neural) blockade will abolish insulin-mediated suppression of C-peptide, attenuating α-cell glucagon secretion during hypoglycemia, and that β-adrenergic (hormonal) blockade will have no effect. Glucose counterregulatory responses will be measured during hyperinsulinemic euglycemic-hypoglycemic clamps on three occasions with randomized, double-blind administration of the α-adrenergic blocker phentolamine, the β-adrenergic blocker propranolol, or placebo. The demonstration of neural rather than hormonal regulation of the transplanted islet cell response to hypoglycemia is critical for understanding the mechanism for protection from hypoglycemia afforded by intrahepatically transplanted islets.

Glucose counterregulation has not been studied in type 1 diabetic recipients of extrahepatic islet transplantation. Comparison of glucose counterregulatory responses measured during hyperinsulinemic euglycemic-hypoglycemic clamps will be compared to those obtained from type 1 diabetic recipients of intrahepatic islet transplantation studied under the placebo condition above.

Glucose counterregulation has not been directly compared between recipients of intrahepatic auto- and allo-islet transplantation. Direct comparison of glucose counterregulatory responses under the same experimental conditions is required to understand whether mechanisms other than the glucagon response may be important to the reported hypoglycemia affecting pancreatectomized recipients of islet auto-transplantation.

Study Timeline

• Study Start: 2017-01-20
• Study First Submitted: 2017-02-28
• Study First Submitted QC: 2017-03-08
• Study First Posted: 2017-03-15
• Primary Completion: 2019-04-30
• Status Verified: 2025-02
• Last Update Submitted: 2025-02-11
• Last Update Posted: 2025-02-13
• Study Completion: 2025-12-31

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 11

Inclusion Criteria

GROUP 1

1. Male and female subjects age 21 to 65 years of age.
2. Subjects who are able to provide written informed consent and to comply with the procedures of the study protocol.
3. Clinical history compatible with type 1 diabetes with onset of disease at < 40 years of age and insulin-dependent for > 10 years at the time of islet transplantation > 6 months before study.
4. Stable islet graft function defined by C-peptide > 0.5 ng/ml and insulin-independent or insulin-dependent with daily insulin requirement < 0.2 units/kg•d to maintain HbA1c < 7.0%.
5. Use of standard immunosuppression consisting of tacrolimus with or without sirolimus or mycophenolic acid. Substitutions of tacrolimus with cyclosporine, and of sirolimus or mycophenolic acid with azathioprine are permissible if stable for over 3 months. Prednisone is allowable if no more than 5 mg daily.

Exclusion Criteria

GROUP 1

1. BMI ≥ 30 kg/m2.
2. Insulin requirement of ≥ 0.2 units/kg•day.
3. HbA1c ≥ 7.0%.
4. Uncontrolled hypertension: systolic blood pressure > 160 mmHg or diastolic blood pressure > 100 mmHg.
5. History of cardiovascular disease, including coronary artery, cerebrovascular or peripheral vascular disease, or current use of β-blocker therapy.
6. Bronchial asthma.
7. Abnormal kidney function: Estimated glomerular filtration rate (eGFR) < 60 ml/min/1.73 m2.
8. Abnormal liver function: persistent elevation of liver function tests > 1.5 times the upper limit of normal.
9. Untreated hypothyroidism, Addison's disease, or Celiac disease.
10. Anemia: baseline hemoglobin concentration < 11 g/dl in women and < 12 g/dl in men.
11. Presence of a seizure disorder not related to prior severe hypoglycemia.
12. Use of glucocorticoids greater than 5 mg of prednisone daily, or an equivalent physiologic dose of hydrocortisone.
13. For female participants of child-bearing potential: Positive pregnancy test, presently breast-feeding, or unwillingness to use effective contraceptive measures for the duration of study participation. Oral contraceptives, intra-uterine devices, Norplant®, Depo-Provera®, and barrier devices with spermicide are acceptable contraceptive methods; condoms used alone are not acceptable.
14. Treatment with any anti-diabetic medication other than insulin within 4 weeks of enrollment.
15. Use of any investigational agents within 4 weeks of enrollment.
16. Any medical condition that, in the opinion of the PI, will interfere with the safe completion of the study

Inclusion Criteria GROUP 2

1. Male and female subjects age 21 to 65 years of age.
2. Subjects who are able to provide written informed consent and to comply with the procedures of the study protocol.
3. Clinical history compatible with type 1 diabetes with onset of disease at < 40 years of age and insulin-dependent for > 10 years at the time of islet transplantation > 6 months before study.
4. Stable islet graft function defined by C-peptide > 0.5 ng/ml and insulin-independent or insulin-dependent with daily insulin requirement < 0.2 units/kg•d to maintain HbA1c < 7.0%.
5. Use of standard immunosuppression consisting of tacrolimus with or without sirolimus or mycophenolic acid. Substitutions of tacrolimus with cyclosporine, and of sirolimus or mycophenolic acid with azathioprine are permissible if stable for over 3 months. Prednisone is allowable if no more than 5 mg daily.

Exclusion Criteria:

GROUP 2

1. BMI ≥ 30 kg/m2.
2. Insulin requirement of ≥ 0.2 units/kg•day.
3. HbA1c ≥ 7.0%.
4. Uncontrolled hypertension: systolic blood pressure > 160 mmHg or diastolic blood pressure > 100 mmHg.
5. Active cardiovascular disease, including coronary artery, cerebrovascular or peripheral vascular disease.
6. Abnormal kidney function: eGFR < 60 ml/min/1.73 m2.
7. Abnormal liver function: persistent elevation of liver function tests > 1.5 times the upper limit of normal.
8. Untreated hypothyroidism, Addison's disease, or Celiac disease.
9. Anemia: baseline hemoglobin concentration < 11 g/dl in women and < 12 g/dl in men.
10. Presence of a seizure disorder not related to prior severe hypoglycemia.
11. Use of glucocorticoids greater than 5 mg of prednisone daily, or an equivalent physiologic dose of hydrocortisone.
12. For female participants of child-bearing potential: Positive pregnancy test, presently breast-feeding, or unwillingness to use effective contraceptive measures for the duration of study participation. Oral contraceptives, intra-uterine devices, Norplant®, Depo-Provera®, and barrier devices with spermicide are acceptable contraceptive methods; condoms used alone are not acceptable.
13. Treatment with any anti-diabetic medication other than insulin within 4 weeks of enrollment.
14. Use of any investigational agents within 4 weeks of enrollment.
15. Any medical condition that, in the opinion of the PI, will interfere with the safe completion of the study

Inclusion Criteria GROUP 3

Patients who meet all of the following criteria are eligible for participation in Group 3 of this study:

1. Male and female subjects age 21 to 65 years of age.
2. Subjects who are able to provide written informed consent and to comply with the procedures of the study protocol.
3. Clinical history compatible with total pancreatectomy and autologous islet transplantation > 6 months before study.
4. Stable islet graft function defined by C-peptide > 0.5 ng/ml and insulin-independent or insulin-dependent with daily insulin requirement < 0.2 units/kg•d to maintain HbA1c < 7.0%.

Exclusion Criteria:

GROUP 3

1. BMI ≥ 30 kg/m2.
2. Insulin requirement of ≥ 0.2 units/kg•day.
3. HbA1c ≥ 7.0%.
4. Uncontrolled hypertension: systolic blood pressure > 160 mmHg or diastolic blood pressure > 100 mmHg.
5. Active cardiovascular disease, including coronary artery, cerebrovascular or peripheral vascular disease.
6. Abnormal kidney function: eGFR < 60 ml/min/1.73 m2.
7. Abnormal liver function: persistent elevation of liver function tests > 1.5 times the upper limit of normal.
8. Anemia: baseline hemoglobin concentration < 11 g/dl in women and < 12 g/dl in men.
9. Presence of a seizure disorder not related to prior severe hypoglycemia.
10. Use of glucocorticoids greater than 5 mg of prednisone daily, or an equivalent physiologic dose of hydrocortisone.
11. For female participants of child-bearing potential: Positive pregnancy test, presently breast-feeding, or unwillingness to use effective contraceptive measures for the duration of study participation. Oral contraceptives, intra-uterine devices, Norplant®, Depo-Provera®, and barrier devices with spermicide are acceptable contraceptive methods; condoms used alone are not acceptable.
12. Treatment with any anti-diabetic medication other than insulin within 4 weeks of enrollment.
13. Use of any investigational agents within 4 weeks of enrollment.
14. Any medical condition that, in the opinion of the PI, will interfere with the safe completion of the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: FACTORIAL

Arm && Interventions

Group	Intervention	Description
Group 1- Placebo Intra-hepatic islet	Placebo	Placebo in 100mL NSS. Infuse Intravenously at 0.0095 ML/KG/MIN. 1 x only via intravenous infusion over 3.5 hours, starting 30 min before conduct of a hyperinsulinemic euglycemic (90 min) followed by hypoglycemia (90 min) clamp.
Group 1-Propranolol Intra-hepatic islet	Propranolol	The dose of propranolol will be 0.48 μg/kilogram•minute, which will provide a total dose of 0.10 mg/kg. It will be administered 1 x only via intravenous infusion over 3.5 hours, starting 30 min before conduct of a hyperinsulinemic euglycemic (90 min) followed by hypoglycemia (90 min) clamp.
Group 1-Phentolamine Intra-hepatic islet	Phentolamine	The dose of phentolamine will be 0.95 μg/kg•min, which will provide a total dose of 0.20 mg/kg. It will be administered 1 x only via intravenous infusion over 3.5 hours, starting 30 min before conduct of a hyperinsulinemic euglycemic (90 min) followed by hypoglycemia (90 min) clamp.

Primary Outcome Measures

Name	Time	Method
C-PEPTIDE suppression during hyperinsulinemia euglycemia.	For C-peptide at the 60-90 time-point during the hyperinsulinemic euglycemic-hypoglycemic clamp.	The primary outcome measures will be the levels of C-peptide during hyperinsulinemia euglycemia.
GLUCAGON activation during hyperinsulinemia hypoglycemia.	For Glucagon at the 150-180 minute time-point during the hyperinsulinemic euglycemic-hypoglycemic clamp.	The primary outcome measures will be the levels of glucagon during hyperinsulinemia hypoglycemia.

Secondary Outcome Measures

Name	Time	Method
EPINEPHRINE during hyperinsulinemia hypoglycemia.	During metabolic testing in the 150-180 minute time-point of the hyperinsulinemic euglycemic-hypoglycemic clamp.	Secondary outcome measures will include levels of epinephrine during hyperinsulinemia hypoglycemia.
Rates of ENDOGENOUS GLUCOSE PRODUCTION during hyperinsulinemia hypoglycemia.	During metabolic testing in the 150-180 minute time-point of the hyperinsulinemic euglycemic-hypoglycemic clamp.	Secondary outcome measures will include rates of endogenous glucose production during hyperinsulinemia hypoglycemia
AUTONOMIC SYMPTOMS during hyperinsulinemia	During metabolic testing; this symptom questionnaire will be asked at the following time points: -15min, -1min, 30min, 60min,75min, 90min,120min, 150min, 165min, 180min.	Secondary outcome measures will include levels of autonomic symptoms during hyperinsulinemia hypoglycemia. Autonomic symptoms will be measured by answering a short symptoms questionnaire with a level scale of 0-5.

Trial Locations

Locations (1)

University of Pennsylvania - Institute for Diabetes, Obesity and Metabolism; 🇺🇸 Philadelphia, Pennsylvania, United States