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KOrea Renal Biobank NEtwoRk System TOward NExt-generation Analysis

Multicenter Prospective Cohort of Kidney Biopsy for Glomerular Disease Research

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03929887
Acronym
KORNERSTONE
Enrollment
3000
Registered
2019-04-29
Start date
2019-05-01
Completion date
2028-12-31
Last updated
2020-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glomerular Disease, Minimal Change Disease, IgA Nephropathy, Membranous Nephropathy, Focal Segmental Glomerulosclerosis, Lupus Nephritis, Crescentic Glomerulonephritis

Keywords

Glomerular disease, sample repository, clinical data, digital pathology repository, web-based database

Brief summary

Glomerulonephritis (GN) generates an enormous individual and social economic burden. However, the therapeutic options are largely based on clinical and pathological parameters and the individual response to therapy or prognosis is uncertain. Recently, along with advances in molecular analysis and computational bioinformatics, genomic data from human renal biopsies could provide a strong foundation for the future of precision medicine in nephrology. In response to a request for applications by the Ministry of Health and Welfare of Korea for the creation of Clinical Research Registry, multi-center N network has been established for prospective cohort with kidney biopsy samples (KORNERSTONE). Through this Network the investigators hope to understand the fundamental biology of glomerulonephritis and aim to bank long-term observational data and corresponding biological data including genomic data from kidney tissues, and kidney pathologic data which is digitalized This database is archived to a web-based platform to access easily and further enrich for researchers.

Detailed description

Glomerulonephritis (GN) such as Minimal change disease (MCD), focal segmental glomerulosclerosis (FSGS), Membranous nephropathy (MN), and Immunoglobulin A nephropathy (IgAN) has quite a common clinical presentation often results in renal insufficiency which generates an enormous individual and social economic burden. However, the therapeutic options are largely based on clinical and pathological parameters and the individual response to therapy or prognosis is uncertain. Recently, along with advances in molecular analysis and computational bioinformatics, genomic data from human renal biopsies could provide a strong foundation for the future of precision medicine in nephrology. In response to a request for applications by the Ministry of Health and Welfare of Korea for the creation of Clinical Research Registry, a number of universities joined together to establish Korean Kidney Biopsy Network (KORNERSTONE). Through this Network the investigators hope to understand the fundamental biology of glomerulonephritis and aim to bank long-term observational data and corresponding biological data including genomic data from kidney tissues, and kidney pathologic data which is digitalized This database is archived to a web-based platform to access easily and further enrich for researchers. ============ \<Patient clinical data will be collected as follows\> 1. Blood tests: CBC, Chemistry (Ca, P, Glucose, Total protein, Albumin, Uric acid), Electrolyte, Renal function (BUN, Creatinine, eGFR), Liver function (AST, ALT) 2. Immunologic blood tests: Complement 3, Complement 4, ASO, RF, Cryoglobulin, dsDNA, ANA 3. Urine tests: Urinalysis, Urine protein, Urine albumin, Urine creatinine 4. Radiologic tests: Kidney USG, Abdominal-pelvis computed tomography 5. Pathologic results 6. Treatment informations: treatment status, drug type, treatment duration 7. Quality of life questionnaire: Kidney Disease and Quality of Life Short Form survey (adults), PedsQL 4.0 Generic Core Scales (pediatrics) 8. Dietary questionnaire

Interventions

Patients scheduled to undergo a clinically indicated kidney biopsy will be requested to consent to an additional renal core and various patient-derived samples.

Sponsors

Chung-Ang University Hosptial, Chung-Ang University College of Medicine
CollaboratorOTHER
KangWon National University Hospital
CollaboratorOTHER
Keimyung University Dongsan Medical Center
CollaboratorOTHER
SMG-SNU Boramae Medical Center
CollaboratorOTHER
Seoul National University Bundang Hospital
CollaboratorOTHER
Severance Hospital
CollaboratorOTHER
Ministry of Health & Welfare, Korea
CollaboratorOTHER_GOV
Seoul National University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Inclusion criteria * Patient suspected of glomerular disease who received kidney biopsy in participating university medical centers * Children (age\<18 years) also included 2.

Exclusion criteria

- Patients who previously received a kidney transplant

Design outcomes

Primary

MeasureTime frameDescription
Death60 monthsDocumentation of death from any cause
Deterioration of renal outcomes60 months1. Doubling of serum creatinine compared to baseline serum creatinine 2. 30% decline in follow-up estimated GFR (using the MDRD equation and/or the CKD-EPI equation) compared to baseline measurement 3. End stage renal disease defined as estimated GFR ≤10cc/min, initiation of maintenance dialysis or kidney transplantation.
Improvement of clinical outcomes60 monthsRemission of glomerulonephritis and proteinuria \<0.3g/day (pateint who have proteinuria\<0.3g/day at baseline have no improvement in clinical outcomes)

Secondary

MeasureTime frameDescription
Hospitalization60 monthsDocumented hospital admission, including observation for ≥24 hours.
Emergency Department/ Observation Unit Visit60 monthsDocumented visit to an emergency department or observation unit that does not lead to hospitalization and is less than 24 hours.
Malignancies60 monthsAny cancer diagnosis of the skin, hematopoietic system, or solid organ after enrollment
New Onset Diabetes60 monthsDiagnosis of diabetes as indicated by 1 or more of the following not present at enrollment 1. Documented diagnosis of diabetes in medical record 2. Casual (non-fasting) blood glucose \> 200 mg/dL c) Fasting blood glucose \> 126 mg/dL d) 2 hour glucose \> 200 after oral glucose tolerance test e) chronic use (\>6 mos) hypoglycemic therapy outside of pregnancy f) Hemogloblin A1C \>= 6.5%
Cardiovascular/Cerebrovascular event60 monthsMyocardial infarction; Congestive heart failure; Primary intractable serious arrhythmia; Peripheral vascular disease; Ischemic cerebrovascular accident; Hemorrhagic cerebrovascular accident; Thromboembolic event
Infections, Serious and Systemic60 monthsDocumented infection of any vital organ requiring the use of parenteral and/or oral antibiotics.
Acute Kidney Injury60 monthsDocumented diagnosis of acute kidney injury as defined by the RIFLE criteria and/or renal failure requiring renal replacement therapy \<3 months.

Countries

South Korea

Contacts

Primary ContactYong Chul Kim, MD,PhD.
imyongkim@gmail.com+82-10-8874-7429
Backup ContactEunyoung Kim
irish-key@nate.com+82-2-6072-5188

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026