Phase 4
Completed N=31
Linagliptin's Effect on CD34+ Stem Cells
Type 2 Diabetes · Impaired Renal Function
Source: ClinicalTrials.gov NCT02467478 ↗
Enrolled (actual)
31
Serious AEs
6.5%
Results posted
Jan 2023
Primary outcomePrimary: Cellular Markers — 1.48; 2.48; 1.43; 2.4 Fold Change
◆ Published Evidence
Established
46citations · ~8 / year
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.
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
Linked Publications
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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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Cellular Markers |
1.48; 2.48; 1.43; 2.4; 1.13; 1.15 | — |
| PRIMARY Urinary Function Marker in CKD |
51.12; 39.70 | — |
| SECONDARY Serum Endothelial Inflammatory Markers |
2.18; 5.09 | — |
| SECONDARY Serum Endothelial Inflammatory Markers |
2.18; 5.09 | — |
| SECONDARY Fasting Lipid Profile |
171.45; 159.69; 127.76; 124.31 | — |
| SECONDARY Glycemic Control |
7.27; 6.66 | — |
| SECONDARY Glycemic Control: Fasting Glucose |
129.68; 109.93 | — |
| SECONDARY Glycemic Control: Insulin |
20.82; 20.52 | — |
| SECONDARY Adiposity |
30.6; 31.2 | — |
| SECONDARY Estimation of Creatinine Clearance |
84.12; 79.46 | — |
| SECONDARY Pulse Wave Analysis |
21.37; 22.33; 24.17; 24.93 | — |
| SECONDARY Pulse Wave Velocity |
10.23; 10.53 | — |
| SECONDARY Resting Metabolic Rate (RMR) |
1650.07; 1657.6 | — |
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 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.
Data sourced from ClinicalTrials.gov (NCT02467478) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.