CROCODILE: Control of Renal Oxygen Consumption, Mitochondrial Dysfunction, and Insulin Resistance

Sponsor
University of Colorado, Denver (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04074668
Collaborator
Juvenile Diabetes Research Foundation (Other)
58
1
34.5
1.7

Study Details

Study Description

Brief Summary

Type 1 diabetes (T1D) is a complex metabolic disorder with many pathophysiological disturbances including insulin resistance (IR) and mitochondrial dysfunction which are causally related to the development of diabetic kidney disease (DKD) and which contribute to reduced life expectancy. Renal hypoxia, stemming from a potential metabolic mismatch between increased renal energy expenditure and impaired substrate utilization, is increasingly proposed as a unifying early pathway in the development of DKD. By examining the interplay between factors responsible for increased renal adenosine triphosphate (ATP) consumption and decreased ATP generation in young adults with and without T1D, this study hopes to identify novel therapeutic targets to impede the development of DKD in future trials.

The investigators propose to address the specific aims in a cross-sectional study with 30 adults with T1D and 20 controls without a diagnosis of diabetes. For this protocol, participants will complete a one day study visit at Children's Hospital Colorado. Patients will undergo a Dual-energy X-Ray Absorptiometry (DXA) scan to assess body composition, renal Magnetic Resonance Imaging (MRI) to quantify renal oxygenation and perfusion, and a Positron Emission Tomography/Computed Tomography (PET/CT) scan to quantify renal O2 consumption. After the PET and MRI, participants will undergo a hyperinsulinemic-euglycemic clamp to quantify insulin sensitivity. Glomerular Filtration Rate (GFR) and Effective Renal Plasma Flow (ERPF) will be measured by iohexol and PAH clearances during the hyperinsulinemic-euglycemic clamp. To further investigate the mechanisms of renal damage in T1D, two optional procedures are included in the study: 1) kidney biopsy procedure and 2) induction of induced pluripotent stem cells (iPSCs) to assess morphometrics and genetic expression of renal tissue.

Condition or Disease Intervention/Treatment Phase
  • Drug: Aminohippurate Sodium Inj 20%
  • Drug: Iohexol Inj 300 milligrams/milliliter (mg/ml)
  • Radiation: PET/CT Scan
  • Procedure: Renal Biopsy

Study Design

Study Type:
Observational
Actual Enrollment :
58 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
CROCODILE Study: Control of Renal Oxygen Consumption, Mitochondrial Dysfunction, and Insulin Resistance
Actual Study Start Date :
Jan 1, 2020
Actual Primary Completion Date :
May 15, 2022
Anticipated Study Completion Date :
Nov 15, 2022

Arms and Interventions

Arm Intervention/Treatment
Type 1 Diabetes

All participants will undergo DXA scan, magnetic resonance imaging (MRI) studies of the kidneys, PET/CT using 11-C acetate to measure renal oxygen consumption, hyperinsulinemic-euglycemic clamp to quantify insulin sensitivity, and renal clearance testing using iohexol and para-aminohippurate (PAH) to quantify glomerular filtration rate (GFR) and effective renal plasma flow (ERPF).

Drug: Aminohippurate Sodium Inj 20%
Diagnostic aid/agent used to measure effective renal plasma flow (ERPF)
Other Names:
  • Sodium 4-amino hippurate (PAH) inj 20% 2 grams (g)/10 milliliters (mL)
  • Para-aminohippurate
  • Aminohippuric acid
  • Drug: Iohexol Inj 300 milligrams/milliliter (mg/ml)
    Diagnostic aid/agent used to measure glomerular filtration rate (GFR)
    Other Names:
  • omnipaque 300
  • Radiation: PET/CT Scan
    Imaging used to visualize the kidneys and quantify renal metabolic activity

    Procedure: Renal Biopsy
    Minimally invasive outpatient procedure to obtain renal tissue after ultrasound visualization.

    Healthy Controls

    All participants will undergo DXA scan, magnetic resonance imaging (MRI) studies of the kidneys, PET/CT using 11-C acetate to measure renal oxygen consumption, hyperinsulinemic-euglycemic clamp to quantify insulin sensitivity, and renal clearance testing using iohexol and para-aminohippurate (PAH) to quantify glomerular filtration rate (GFR) and effective renal plasma flow (ERPF).

    Drug: Aminohippurate Sodium Inj 20%
    Diagnostic aid/agent used to measure effective renal plasma flow (ERPF)
    Other Names:
  • Sodium 4-amino hippurate (PAH) inj 20% 2 grams (g)/10 milliliters (mL)
  • Para-aminohippurate
  • Aminohippuric acid
  • Drug: Iohexol Inj 300 milligrams/milliliter (mg/ml)
    Diagnostic aid/agent used to measure glomerular filtration rate (GFR)
    Other Names:
  • omnipaque 300
  • Radiation: PET/CT Scan
    Imaging used to visualize the kidneys and quantify renal metabolic activity

    Procedure: Renal Biopsy
    Minimally invasive outpatient procedure to obtain renal tissue after ultrasound visualization.

    Outcome Measures

    Primary Outcome Measures

    1. Renal Oxygenation [30 minutes]

      Blood oxygen level dependent (BOLD) MRI

    2. Renal Perfusion [30 minutes]

      Arterial Spin Labeling (ASL) MRI

    3. Renal Oxygen Consumption [30 minutes]

      11-C Acetate PET/CT

    4. Insulin Sensitivity [4.5 hours]

      Hyperinsulinemic-Euglycemic Clamp

    5. Mitochondrial Function [5 minutes]

      Blood draw for mitochondrial DNA copy number

    6. Mitochondrial Function [5 minutes]

      Blood draw for untargeted metabolite assessment of the tricyclic acid (TCA) cycle

    7. Mitochondrial Function [5 minutes]

      Blood draw for targeted assessment and quantification of glucose oxidation using an established metabolite panel

    8. Mitochondrial Function [5 minutes]

      Blood draw for untargeted metabolite assessment of Free Fatty Acid (FFA) oxidation

    Secondary Outcome Measures

    1. Glomerular Filtration Rate (GFR) [3 hours]

      Iohexol Clearance Study

    2. Effective Renal Plasma Flow (ERPF) [2.5 hours]

      PAH Clearance Study

    3. Renin-Angiotensin-Aldosterone-System Activity [5 minutes]

      Blood draw for Plasma Renin levels

    4. Renin-Angiotensin-Aldosterone-System Activity [5 minutes]

      Blood draw for Angiotensin II levels

    5. Renin-Angiotensin-Aldosterone-System Activity [5 minutes]

      Blood draw for Copeptin levels

    6. Kidney Injury Biomarkers [5 minutes]

      Blood draw for Tyrosine Lysine Leucine-40 (YKL-40) levels

    7. Kidney Injury Biomarkers [5 minutes]

      Blood draw for Neutrophil gelatinase-associated lipocalin (NGAL) levels

    8. Kidney Injury Biomarkers [5 minutes]

      Blood draw for Kidney Injury Marker 1 (KIM-1) levels

    9. Kidney Injury Biomarkers [5 minutes]

      Blood draw for Interleukin-18 (IL-18) levels

    10. Kidney Injury Biomarkers [5 minutes]

      Blood draw for Tumor Necrosis Factor Receptor 1/2 (TNF-R 1/2) levels

    Other Outcome Measures

    1. Podocyte numerical density and number per glomerulus [4 hours]

      Measured by light microscopy from tissue obtained by renal biopsy

    2. Foot process width of glomeruli [4 hours]

      Measured by electron microscopy from tissue obtained by renal biopsy

    3. Detachment and endothelial fenestration of glomeruli [4 hours]

      Measured by electron microscopy from tissue obtained by renal biopsy

    4. Podocyte volume of glomeruli [4 hours]

      Measured by electron microscopy from tissue obtained by renal biopsy

    5. Number and identity of RNA in kidney cells [4 hours]

      Measured from tissue obtained by renal biopsy

    6. Epigenetic profiling [4 hours]

      Measured from tissue obtained by renal biopsy

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 30 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria -- Type 1 Diabetes:
    • Antibody positive Type 1 Diabetes with duration > 5 years

    • BMI between 18.5 and 30 kg/m2

    • Weight < 350 lbs

    • HbA1c < 11%

    • Hemoglobin >= 12 g/dl

    Exclusion Criteria -- Type 1 Diabetes:
    • Recent diagnosis (within 3 months) of Diabetic Ketoacidosis (DKA)

    • Severe illness

    • Pregnancy, nursing

    • Anemia

    • Allergy to shellfish or iodine

    • Claustrophobia or implantable metal devices (MRI contraindications)

    • High blood pressure (greater than 130/80 mm Hg)

    • Elevated Urine Albumin-to-Creatinine Ratio (UACR) (>30 mg/g) or estimated Glomerular Filtration Rate (eGFR) <90 ml/min/1.73 m2

    • Taking ACE inhibitors (ACEis), Angiotensin receptor blockers (ARBs), diuretics, Sodium Glucose Transporter (SGLT) 1/2 blockers

    Inclusion Criteria -- Healthy Controls:
    • No diagnosis of Type 1 or Type 2 Diabetes

    • BMI between 18.5 and 30 kg/m2

    • Weight < 350 lbs

    • HbA1c < 11%

    • Hemoglobin >= 12 g/dl

    Exclusion Criteria -- Healthy Controls:
    • Severe illness

    • Pregnancy, nursing

    • Anemia

    • Allergy to shellfish or iodine

    • Claustrophobia or implantable metal devices (MRI contraindications)

    • High blood pressure (greater than 130/80 mm Hg)

    • Elevated UACR (>30 mg/g) or eGFR <90 ml/min/1.73 m2

    • Taking ACE inhibitors (ACEis), Angiotensin receptor blockers (ARBs), diuretics, SGLT 1/2 blockers

    Additional exclusion criteria for participants undergoing optional kidney biopsy:
    • Evidence of bleeding disorder or complications from bleeding

    • Use of aspirin, NSAIDS or other blood thinner that cannot be safely stopped for a sufficient time period before and after the biopsy so as to add no additional risk of bleeding

    • Blood urea nitrogen (BUN) > 80 gm/dL

    • INR > 1.4

    • PTT > 35 seconds

    • Hemoglobin (Hgb) < 10 mg/dL

    • Platelet count < 100,000 / µL

    • Uncontrolled or difficult to control hypertension (> 150/90 mmHg at the day of biopsy)

    • eGFR < 40 mL/min/1.73m2

    • Single kidney (either by history, documented by prior imaging or ultrasound performed prior to the biopsy)

    • 2 cm discrepancy between left and right kidney sizes based on largest longitudinal diameter determined by ultrasound performed prior to the biopsy.

    • Kidney size: One or both kidneys < 9 cm

    • Hydronephrosis or other important renal ultrasound findings such as significant stone disease

    • Any evidence of a current urinary tract infection as indicated on day of biopsy

    • Clinical evidence of non-diabetic renal disease

    • Positive urine pregnancy test or pregnancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Children's Hospital Colorado Aurora Colorado United States 80045

    Sponsors and Collaborators

    • University of Colorado, Denver
    • Juvenile Diabetes Research Foundation

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Colorado, Denver
    ClinicalTrials.gov Identifier:
    NCT04074668
    Other Study ID Numbers:
    • 19-1282
    First Posted:
    Aug 30, 2019
    Last Update Posted:
    Jul 21, 2022
    Last Verified:
    Jul 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 21, 2022