Purpose

Acute kidney injury (AKI) and chronic kidney disease (CKD) impose a significant global health burden. Yet, no effective therapies currently exist for AKI, and only a few are available for CKD.

Despite significant effort from industry and academia, development of pharmacologic therapies for AKI and CKD has been hampered by:

Non-predictive animal models The inability to identify and prioritize human targets The limited availability of human kidney biopsy tissue A poor understanding of AKI and CKD heterogeneity Historically, AKI and CKD have been described as single, uniform diseases. However, growing consensus suggests that different disease pathways lead to different subgroups of AKI and CKD (AKIs and CKDs).

Access to human kidney biopsy tissue is a critical first step to define disease heterogeneity and determine the precise molecular pathways that will facilitate identification of specific drug targets and ultimately enable individualized care for people with AKI and CKD.

A number of research centers across the United States are collaborating to bring state-of-the-art technologies together to:

The KPMP is made up of three distinct, but highly interactive, activity groups:

Category

IRB Number
20190453HU
NCT Number
NCT04334707
Sponsor
University of Washington -



Study Contact

Principal Investigator
Kumar Sharma

Guanshi Zhang
210-450-3193
zhangg3@uthscsa.edu



Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

    Diabetic kidney disease (DKD) - Diagnosis of diabetes mellitus (type 1 or 2) established by at least one of the following criteria: - Hemoglobin A1C greater than or equal to 6.5%, confirmed with a repeat test within the past year - Fasting blood sugar greater than or equal to 126 mg/dL, confirmed with a repeat test within the past year - Use of glucose-lowering therapy (insulin or oral or other subcutaneous agents) - International Classification of Diseases (ICD) 9/10 diagnostic code for diabetes - Evidence of persistent kidney damage, manifest as any of the following present on at least two clinic assessments prior to enrollment and at least 3 months apart and excluding subjects with acute medical illnesses and changing kidney function: - Estimated glomerular filtration rate 30-59 mL/min/1.73m2 - Estimated glomerular filtration rate greater than or equal to 60 mL/min/1.73m2 with urine albumin excretion greater than or equal to 30 mg/g creatinine (or mg/day) - Estimated glomerular filtration rate greater than or equal to 60 mL/min/1.73m2 with urine protein excretion greater than or equal to 150 mg/g creatinine (or mg/day) Hypertension-associated Chronic Kidney Disease (H-CKD) Inclusion Criteria - Diagnosis of hypertension (HTN) established by at least one of the following criteria: - BP greater than 140/90 mmHg measured on three occasions over at least 1 month - Taking antihypertensive medication for blood pressure (BP) control - International Classification of Diseases (ICD) 9/10 diagnostic code for hypertension - Evidence of persistent kidney damage, manifested as any of the following present on at least two assessments at least 3 months apart and excluding subjects with acute medical illnesses and changing kidney function: - Estimated glomerular filtration rate 30-59 mL/min/1.73m2 on two assessments at least 3 months apart with albuminuria or proteinuria less than 2000 mg/g creatinine (or mg/day) - Estimated glomerular filtration rate greater than or equal to 60 mL/min/1.73m2 with urine albumin excretion 30-2000 mg/g creatinine (or mg/day) - Estimated glomerular filtration rate greater than or equal to 60 mL/min/1.73m2 with urine protein excretion 150-2000 mg/g creatinine (or mg/day) Acute Kidney Injury Subjects Inclusion Criteria All three of the following criteria must be met: - Baseline estimated glomerular filtration rate greater than 45 mL/min/1.73m2. Baseline defined by the median of the last three outpatient serum creatinine measurements from day 7 to 365 prior to enrollment. - If only two measurements obtained within this window, the two results will be averaged. - If only one measurement was obtained within this window, this result will be used - If baseline is missing the potential participant can be enrolled with an estimated baseline, but only if there is no past medical history of chronic kidney disease. - Elevated serum creatinine (greater than or equal to 1.5 times baseline as defined above). - And at least ONE of the following: - A repeat serum creatinine within 48 hours of initial serum creatinine, showing a further increase of 0.3 mg/dL - Positive kidney injury urine biomarker, as defined by any of the following: - NGAL level greater than or equal to 150 ng/mL by ELISA or clinical analyzer - KIM1 level greater than or equal to 2.8 ng/mL by ELISA - TIMP2 x IGFBP7 greater than or equal to 2.0 by NephroCheck® - Urine microscopy suggestive of acute tubular necrosis defined as a urine microscopy score of greater than or equal to 2. - greater than or equal to 1 Renal Tubular Epithelial cells (RTE) per high powered field (HPF) AND greater than or equal to 1 granular cast/ low powered field (LPF); or - greater than or equal to 5 Renal Tubular Epithelial cells (RTE) per high powered field (HPF); or - greater than or equal to 5 granular cast/ low powered field (LPF) General Exclusion Criteria: - Under

Exclusion Criteria

    - Under 18 years of age - Body Mass Index (BMI) greater than 40 kg/m2 - Allergy to iodinated contrast (any reaction) - Pregnancy - Malignancy - Receiving active chemotherapy or radiation to treat malignancy (except for nephrectomy tissue for reference and feasibility studies) - Transplant recipient (includes solid transplant and bone marrow) - Additional vulnerable individuals (incarcerated, institutionalized, or otherwise unable to participate in the study) - Inability to provide informed consent - Clinical diagnosis of kidney disease from an autoimmune disease, dysproteinemia, viral disease or glomerular disease other than DKD or H-CKD - Unwilling to receive blood transfusion (if needed)

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective
Condition
  • Acute Kidney Failure
  • Acute Kidney Insufficiency
  • Acute Renal Failure
  • Acute Renal Injury
  • Acute Renal Insufficiency
  • Kidney Failure, Acute
  • Kidney Insufficiency, Acute
  • Renal Failure, Acute
  • Renal Insufficiency, Acute
  • Chronic Kidney Diseases
  • Chronic Kidney Insufficiency
  • Chronic Renal Diseases
  • Chronic Renal Insufficiency
  • Kidney Insufficiency, Chronic
  • Arm Groups

    ArmDescriptionIntervention

    Chronic Kidney Diseases Cohort

    High priority populations include CKD in the setting of diabetes (diabetic kidney disease, DKD) and hypertension-associated CKD (H-CKD). A special population of people with long-standing type 1 diabetes (more than 25 years) who remain free of clinically-evident DKD will also be included.
  • Procedure: Kidney Biopsy

    A kidney biopsy is a procedure that involves taking a small piece of kidney tissue for examination with a microscope. A licensed health care provider will perform a kidney biopsy.

    Other names:

    • Renal Biopsy
    • Laparotomy

  • Acute Kidney Injury Cohort

    The focus will be on acute intrinsic non-glomerular disease, primarily on acute tubular necrosis (ATN). KPMP will also include a special population of patients at risk for AKI or with early AKI captured by an open (surgical) kidney biopsy performed at the time of clinically indicated laparotomy.
  • Procedure: Kidney Biopsy

    A kidney biopsy is a procedure that involves taking a small piece of kidney tissue for examination with a microscope. A licensed health care provider will perform a kidney biopsy.

    Other names:

    • Renal Biopsy
    • Laparotomy