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.
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
Study Type
OBSERVATIONAL
Enrollment
3,000
Patients scheduled to undergo a clinically indicated kidney biopsy will be requested to consent to an additional renal core and various patient-derived samples.
KangWon National University Hospital
Chuncheon, South Korea
RECRUITINGKeimyung University Dongsan Medical Center
Daegu, South Korea
RECRUITINGChung-Ang University Hosptial
Seoul, South Korea
RECRUITINGSeoul National University Hospital
Seoul, South Korea
RECRUITINGSeverance Hospital
Seoul, South Korea
RECRUITINGSMG-SNU Boramae Medical Center
Seoul, South Korea
RECRUITINGDeath
Documentation of death from any cause
Time frame: 60 months
Deterioration of renal outcomes
1. 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.
Time frame: 60 months
Improvement of clinical outcomes
Remission of glomerulonephritis and proteinuria \<0.3g/day (pateint who have proteinuria\<0.3g/day at baseline have no improvement in clinical outcomes)
Time frame: 60 months
Malignancies
Any cancer diagnosis of the skin, hematopoietic system, or solid organ after enrollment
Time frame: 60 months
Infections, Serious and Systemic
Documented infection of any vital organ requiring the use of parenteral and/or oral antibiotics.
Time frame: 60 months
Acute Kidney Injury
Documented diagnosis of acute kidney injury as defined by the RIFLE criteria and/or renal failure requiring renal replacement therapy \<3 months.
Time frame: 60 months
Hospitalization
Documented hospital admission, including observation for ≥24 hours.
Time frame: 60 months
Emergency Department/ Observation Unit Visit
Documented visit to an emergency department or observation unit that does not lead to hospitalization and is less than 24 hours.
Time frame: 60 months
Cardiovascular/Cerebrovascular event
Myocardial infarction; Congestive heart failure; Primary intractable serious arrhythmia; Peripheral vascular disease; Ischemic cerebrovascular accident; Hemorrhagic cerebrovascular accident; Thromboembolic event
Time frame: 60 months
New Onset Diabetes
Diagnosis 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%
Time frame: 60 months
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