Linagliptin's Effect on CD34+ Stem Cells
Primary Purpose
Type 2 Diabetes, Impaired Renal Function
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Linagliptin
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Type 2 Diabetes focused on measuring Diabetes Mellitus, Type 2, Endothelial cells, Cellular biomarker, endothelial dysfunction, CD34+, Impaired renal function
Eligibility Criteria
Inclusion Criteria:
- Adults aged 30-70 years
- Diagnosis of type 2 diabetes within the previous 15 years using criteria of the American Diabetes Association
- Currently being treated with 1-2 grams/day of metformin, or insulin or both stably
- Hemoglobin A1c (HbA1C) between 6.5% to 10.0% (both inclusive)
- Body Mass Index (BMI) between 25 and 39.9 kg/m2 (both inclusive)
- Chronic Kidney disease (CKD) Stages 1-3, Creatinine clearance (CrCl) less than 90 and more than 29
Exclusion Criteria:
- Type 1 diabetes
- History of Diabetic Ketoacidosis (DKA) or hyperosmolar nonketotic coma
- Hemoglobinopathies with low hematocrit (Below 28 Units)
- History of pancreatitis
- History of cancer within the past 5 years (except basal cell carcinoma)
- Previous cardiovascular or cerebrovascular event within 6 months of screening or active or clinically significant coronary and/or Peripheral Vascular Disease (PVD)
- Statin use started in the last 3 month
- Current use of oral or injectable anti-diabetic medication other than Metformin and insulin
- Consistent use of steroids within the last 3 months
- Any active wounds, or surgery within the past 3 months
- Inflammatory disease, or the chronic use of anti-inflammatory drugs within the past 3 months
- Untreated hyper/hypothyroidism
- Contraindications to moderate exercise
- Implanted devices that might interact with the tanita scale
- Pre-existing liver disease and/or Alanine aminotransferase (ALT) and Aspartate Aminotransferase (AST) > 2.5 times Under the Normal Limits (UNL)
- Untreated Systolic blood pressure > 140 mmHg or diastolic blood pressure> 90 mmHg
- Serum creatinine levels ≥ 2.0
- CKD Stages 4 and 5 (estimated CrCl <30 mL/min)
- Triglycerides > 450 mg/dL
- Known allergies or hypersensitivities to Linagliptin or Dipeptidyl peptidase-4 (DDP-4) inhibitors
- Treatment with cytochrome p450 (CYP 3A4) inhibitors
- Women of child bearing age who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study
- Prisoners or subjects that are involuntarily incarcerated
- Subjects who are compulsorily detained for treatment of either a psychiatric or physical (e.g. infectious disease) illness
- Additionally, patients who are active smokers, patients who are pregnant, nursing women, and post-menopausal women who are on hormone replacement therapy will be excluded.
Sites / Locations
- The George Washington University Medical Faculty Associates
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Placebo
Linagliptin
Arm Description
Matching placebo 1 pill daily for 12 weeks
Linagliptin 5mg once daily for 12 weeks
Outcomes
Primary Outcome Measures
Cellular Markers
The investigators will use participants' peripheral blood derived CD34+ cells looking at number, function, and gene expression. Post Linagliptin will be compared to pre Linagliptin measurements. Here we report fold changes in protein populations as determined by ELISA.
Urinary Function Marker in CKD
We measure using microalbumin/creatinine ratio provided from a random spot urine sample.
Secondary Outcome Measures
Serum Endothelial Inflammatory Markers
Serum endothelial inflammatory markers included here: high sensitivity C-reactive protein (hs-CRP)
Serum Endothelial Inflammatory Markers
Serum endothelial inflammatory markers included here: Interleukin 6 (IL-6)
Fasting Lipid Profile
Measured through serum biochemistry Lipid Panel
Glycemic Control
Glycemic control is evaluated by measuring HbA1c levels to gauge changes in blood sugar control over last ~90 days
Glycemic Control: Fasting Glucose
Glycemic control is evaluated by measuring fasting blood glucose at time of measurement
Glycemic Control: Insulin
Glycemic control is evaluated by measuring insulin levels at the time of the visit
Adiposity
Measured using the Tanita Body Composition Analyzer scale, measured as percentage body fat.
Estimation of Creatinine Clearance
Measured via blood biochemistry eGFR, an alternative measurement to spot urine urine microalbumin/creatinine ratio presented above
Pulse Wave Analysis
Vessel health is assessed by looking at Arterial stiffness. Augmentation index (AI) is defined as the ratio of the augmentation pressure to the pulse pressure, times 100, to give a percentage. Augmentation index 75 normalizes this value to an estimate of the AI at a heart rate of 75bpm. We used Vascular Flow and wave measurement equipment, SphygmoCor Central Pressure system from AtCor.
Pulse Wave Velocity
Vessel health is assessed by looking at Arterial stiffness. Pulse wave velocity (PWV) measures the delay between the pulse registered at the femoral artery from the pulse at the carotid. The difference in distance between these two measurement points from the aortic notch is divided by this delay to give a speed. In stiffer, less healthy vessels, the PWV is increased. We used Vascular Flow and wave measurement equipment, SphygmoCor Central Pressure system from AtCor to perform this calculation.
Resting Metabolic Rate (RMR)
(RMR, similar to Resting Energy expenditure measurement): Evaluation of changes in Basal Metabolic Rate
Full Information
NCT ID
NCT02467478
First Posted
June 8, 2015
Last Updated
December 21, 2022
Sponsor
George Washington University
Collaborators
Boehringer Ingelheim
1. Study Identification
Unique Protocol Identification Number
NCT02467478
Brief Title
Linagliptin's Effect on CD34+ Stem Cells
Official Title
Role of Linagliptin in Improving Renal Failure by Improving CD34+ Stem Cell Number, Function and Gene Expression in Renal Function Impaired Type 2 Diabetes Patients.
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
April 2015 (Actual)
Primary Completion Date
April 2019 (Actual)
Study Completion Date
December 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
George Washington University
Collaborators
Boehringer Ingelheim
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Type 2 diabetes is a national epidemic. Diabetes has undesirable effects on blood vessels which may contribute to heart disease. Endothelial Progenitor Cells (EPCs) are found in the blood. Research has shown that improving the survival of these special blood cells may decrease the harmful effects of diabetes on blood vessels and reduce or reverse heart disease. Linagliptin is an Food and Drug Administration (FDA) approved prescription medicine used along with insulin or with oral medications to lower blood sugar in people with Type 2 diabetes. It is in a class of diabetes medication called Dipeptidyl peptidase-4 (DPP-4) inhibitors. DPP-4 inhibitors have been shown to increase EPCs in patients with Type 2 diabetes.
Hypothesis: Both type 2 diabetes and Chronic Kidney Disease (CKD) are associated with poor stem cell number and function. Poor viability and function of EPCs in CKD and diabetes The investigators hypothesize that use of Linagliptin (along with Insulin) may help reduce cardiovascular risk by improving EPC survival and function above and beyond adequate glucose metabolism control
Detailed Description
Type 2 diabetes is a national epidemic with significant macro and microvascular complications. Insulin resistance in pre-diabetes and overt diabetes are associated with endothelial dysfunction.
A few studies indicate that stem cells particularly EPCs can act as a suitable bio-marker for monitoring cardiovascular morbidity. In this proposal the investigators suggest that EPCs or CD34 positive cells (defined as CD34/vascular endothelial growth factor receptor 2 (VEGFR2+) cells) can act as a suitable cellular biomarker for estimating and following endothelial dysfunction in early type 2 diabetes patients with CKD. EPCs have been shown to be dysfunctional in both CKD patients and type 2 Diabetes Mellitus (DM) patients.
Linagliptin (TRADJENTA) tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. No dose adjustment is recommended for patients with renal impairment.
EPCs have been used as a regenerative tool in ischemic myocardium and diabetic wound healing. Endothelial dysfunction with associated inflammation may be a consequence of excess intra-cellular super-oxide presence in a setting of diabetes which is a pro-oxidative stress condition ultimately leading to poor EPC function and senescence.
Though lifestyle modification has been proposed as a main stay for prevention and treatment of early type 2 diabetes, several new therapies for diabetes have been developed in recent years. Incretins and incretin mimetics appear to hold promise. Mechanism of positive effect of exercise and oral hypoglycemic agents can be very different.
DPP-4 inhibitors have been shown to increase EPCs in patients with type 2 diabetes reportedly via stromal cell-derived factor 1 (SDF-1) alpha up-regulation. Interestingly, up-regulation of SDF-1 alpha and vascular endothelial growth factor (VEGF), both chemotactic factors increase mobilization and recruitment of EPCs in the face of acute ischemic injury for repair and regeneration.
Several studies have shown positive effect of incretins (Glucagon like peptide, GLP-1) and incretin receptor agonists (GLP-1 receptor agonists) on cardiovascular risk factors in type 2 diabetes patients and even in patients with chronic heart failure and left ventricular dysfunction who do not have diabetes.
DPP-4 Inhibitors may have cardio-protective effects of their own, as they increase bio-availability of endogenous GLP-1. They improve blood flow and nitric oxide production in endothelium. These are unique properties not demonstrated by other oral diabetes medications. The mechanism underlying these effects may be mediated by increased nitric oxide bioavailability but is not completely known. However these beneficial effects appear to be independent of glycemia reduction.
It is however unknown whether Linagliptin will have any positive effect on human EPC function where two prominent cardiovascular risk factors co-exist such as CKD and type 2 diabetes.
Therefore the investigators plan to investigate if Linagliptin can alter function and gene expression of CD34+ cells in a setting of CKD and type 2 diabetes. The investigators choose to look at non geriatric adult population with early type 2 diabetes (less than 10 years of duration) at an early phase of renal impairment (stages 1-3).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes, Impaired Renal Function
Keywords
Diabetes Mellitus, Type 2, Endothelial cells, Cellular biomarker, endothelial dysfunction, CD34+, Impaired renal function
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
31 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Matching placebo 1 pill daily for 12 weeks
Arm Title
Linagliptin
Arm Type
Active Comparator
Arm Description
Linagliptin 5mg once daily for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Linagliptin
Other Intervention Name(s)
TRADJENTA
Intervention Description
5 mg tablet once daily for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
1 tablet daily for 12 weeks
Primary Outcome Measure Information:
Title
Cellular Markers
Description
The investigators will use participants' peripheral blood derived CD34+ cells looking at number, function, and gene expression. Post Linagliptin will be compared to pre Linagliptin measurements. Here we report fold changes in protein populations as determined by ELISA.
Time Frame
Week 12 expression as a fold difference to Week 0
Title
Urinary Function Marker in CKD
Description
We measure using microalbumin/creatinine ratio provided from a random spot urine sample.
Time Frame
12 weeks post beginning Linagliptin or placebo treatment
Secondary Outcome Measure Information:
Title
Serum Endothelial Inflammatory Markers
Description
Serum endothelial inflammatory markers included here: high sensitivity C-reactive protein (hs-CRP)
Time Frame
12 weeks post Linagliptin or Placebo treatment
Title
Serum Endothelial Inflammatory Markers
Description
Serum endothelial inflammatory markers included here: Interleukin 6 (IL-6)
Time Frame
12 weeks post Linagliptin or Placebo treatment
Title
Fasting Lipid Profile
Description
Measured through serum biochemistry Lipid Panel
Time Frame
12 weeks post beginning Linagliptin or placebo treatment
Title
Glycemic Control
Description
Glycemic control is evaluated by measuring HbA1c levels to gauge changes in blood sugar control over last ~90 days
Time Frame
12 weeks post beginning Linagliptin or placebo treatment
Title
Glycemic Control: Fasting Glucose
Description
Glycemic control is evaluated by measuring fasting blood glucose at time of measurement
Time Frame
12 weeks post beginning Linagliptin or placebo treatment
Title
Glycemic Control: Insulin
Description
Glycemic control is evaluated by measuring insulin levels at the time of the visit
Time Frame
12 weeks post beginning Linagliptin or placebo treatment
Title
Adiposity
Description
Measured using the Tanita Body Composition Analyzer scale, measured as percentage body fat.
Time Frame
12 weeks post beginning Linagliptin or placebo treatment
Title
Estimation of Creatinine Clearance
Description
Measured via blood biochemistry eGFR, an alternative measurement to spot urine urine microalbumin/creatinine ratio presented above
Time Frame
12 weeks post beginning Linagliptin or placebo treatment
Title
Pulse Wave Analysis
Description
Vessel health is assessed by looking at Arterial stiffness. Augmentation index (AI) is defined as the ratio of the augmentation pressure to the pulse pressure, times 100, to give a percentage. Augmentation index 75 normalizes this value to an estimate of the AI at a heart rate of 75bpm. We used Vascular Flow and wave measurement equipment, SphygmoCor Central Pressure system from AtCor.
Time Frame
12 weeks post beginning Linagliptin or placebo treatment
Title
Pulse Wave Velocity
Description
Vessel health is assessed by looking at Arterial stiffness. Pulse wave velocity (PWV) measures the delay between the pulse registered at the femoral artery from the pulse at the carotid. The difference in distance between these two measurement points from the aortic notch is divided by this delay to give a speed. In stiffer, less healthy vessels, the PWV is increased. We used Vascular Flow and wave measurement equipment, SphygmoCor Central Pressure system from AtCor to perform this calculation.
Time Frame
12 weeks post beginning Linagliptin or placebo treatment
Title
Resting Metabolic Rate (RMR)
Description
(RMR, similar to Resting Energy expenditure measurement): Evaluation of changes in Basal Metabolic Rate
Time Frame
12 weeks post beginning Linagliptin or placebo treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adults aged 30-70 years
Diagnosis of type 2 diabetes within the previous 15 years using criteria of the American Diabetes Association
Currently being treated with 1-2 grams/day of metformin, or insulin or both stably
Hemoglobin A1c (HbA1C) between 6.5% to 10.0% (both inclusive)
Body Mass Index (BMI) between 25 and 39.9 kg/m2 (both inclusive)
Chronic Kidney disease (CKD) Stages 1-3, Creatinine clearance (CrCl) less than 90 and more than 29
Exclusion Criteria:
Type 1 diabetes
History of Diabetic Ketoacidosis (DKA) or hyperosmolar nonketotic coma
Hemoglobinopathies with low hematocrit (Below 28 Units)
History of pancreatitis
History of cancer within the past 5 years (except basal cell carcinoma)
Previous cardiovascular or cerebrovascular event within 6 months of screening or active or clinically significant coronary and/or Peripheral Vascular Disease (PVD)
Statin use started in the last 3 month
Current use of oral or injectable anti-diabetic medication other than Metformin and insulin
Consistent use of steroids within the last 3 months
Any active wounds, or surgery within the past 3 months
Inflammatory disease, or the chronic use of anti-inflammatory drugs within the past 3 months
Untreated hyper/hypothyroidism
Contraindications to moderate exercise
Implanted devices that might interact with the tanita scale
Pre-existing liver disease and/or Alanine aminotransferase (ALT) and Aspartate Aminotransferase (AST) > 2.5 times Under the Normal Limits (UNL)
Untreated Systolic blood pressure > 140 mmHg or diastolic blood pressure> 90 mmHg
Serum creatinine levels ≥ 2.0
CKD Stages 4 and 5 (estimated CrCl <30 mL/min)
Triglycerides > 450 mg/dL
Known allergies or hypersensitivities to Linagliptin or Dipeptidyl peptidase-4 (DDP-4) inhibitors
Treatment with cytochrome p450 (CYP 3A4) inhibitors
Women of child bearing age who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study
Prisoners or subjects that are involuntarily incarcerated
Subjects who are compulsorily detained for treatment of either a psychiatric or physical (e.g. infectious disease) illness
Additionally, patients who are active smokers, patients who are pregnant, nursing women, and post-menopausal women who are on hormone replacement therapy will be excluded.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sabyasachi Sen, MD, PhD
Organizational Affiliation
Medical Faculty Associates
Official's Role
Principal Investigator
Facility Information:
Facility Name
The George Washington University Medical Faculty Associates
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20037
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
There is no current plan to share IPD with other researchers.
Citations:
PubMed Identifier
32493344
Citation
Awal HB, Nandula SR, Domingues CC, Dore FJ, Kundu N, Brichacek B, Fakhri M, Elzarki A, Ahmadi N, Safai S, Fosso M, Amdur RL, Sen S. Linagliptin, when compared to placebo, improves CD34+ve endothelial progenitor cells in type 2 diabetes subjects with chronic kidney disease taking metformin and/or insulin: a randomized controlled trial. Cardiovasc Diabetol. 2020 Jun 3;19(1):72. doi: 10.1186/s12933-020-01046-z.
Results Reference
derived
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Linagliptin's Effect on CD34+ Stem Cells
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