From Immune System Damage to Podocyte Cell Damage: Prospective Database and Biological Collection of Patients (Children and Adults) With MGLS and HSFP (BiobankSNI)

From Immune System Damage to Podocyte Cell Damage: Prospective Database and Biological Collection of Patients (Children and Adults) With Minimal Glomerular Injury Nephrotic Syndrome (MGLS) and Primary Segmental and Focal Hyalinosis (HSFP)

Idiopathic Nephrotic Syndrome (INS) is a kidney disease characterized by massive proteinuria and hypoalbuminemia. It includes two anatomopathological entities: nephrotic syndrome with minimal glomerular lesions (SNLGM) and primary segmental and focal hyalinosis (PHF). Renal biopsy reveals a fusion of the feet of the podocytes without inflammatory lesions or deposits of immune complexes. Clinical and experimental observations strongly suggest that the immune system and podocyte dysfunction are the two facets of the disease. There are currently no clinical or biological markers to predict the diagnosis of corticosteroid sensitivity, corticosteroid dependence, or risk of recurrence of kidney disease after kidney transplantation. To our knowledge, no prospective studies have been designed to study both immune system alterations and podocyte damage as well as genetic predisposition variants in NIS. Therefore, the use of steroids/immunosuppressive agents is purely empirical with a multitude of side effects.

The objective is to identify and test new therapeutic targets rather than conducting new trials with existing treatments, using either drug candidates or molecules selected by high throughput screening of libraries of repositioning molecules using an appropriate read-out. The biobank may also be used to analyze the effects of conventional treatments on identified new biomarkers. We expect the project to produce original and patentable results with subsequent valuation. Patentability will be anticipated before any publication on the subject. The patent and valorization cells of hospitals, INSERM and Universities will be involved in the results as soon as they are obtained.

Study Overview

• Status: Recruiting
• Conditions: Nephrotic Syndrome
• Intervention / Treatment: Other: blood sample; Other: tissue sample; Other: excreta

• Study Type: Observational
• Enrollment (Anticipated): 144

Contacts and Locations

• Study Contact: Name: Barbara SEITZ POLSKI; Phone Number: 33 4 92 03 55 02; Email: seitz-polski.b@chu-nice.fr

Study Locations

• France
  • Nice, France, 06000
    • Recruiting
    • Nice Hospital
    • Contact: Barbara SEITZ POLSKI; Phone Number: 334 92 03 55 02; Email: seitz-polski.b@chu-nice.fr
    • Principal Investigator: barbara SEITZ POLSKI
    • Sub-Investigator: Vincent ESNAULT
  • Paris, France, 75000
    • Recruiting
    • APHP
    • Principal Investigator: Olivia BOYER
    • Principal Investigator: Georges DESCHENES
    • Contact: Vincent Audard; Phone Number: (33)149814446; Email: vincent.audard@aphp.fr
    • Principal Investigator: Vincent Audard
    • Principal Investigator: Emmanuelle PLAISIER
    • Sub-Investigator: Pierre RONCO
    • Sub-Investigator: Claire DOSSIER
    • Sub-Investigator: Bertrand KNEBELMANN

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 1 year and older (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

patient with Idiopathic Nephrotic Syndrome

Description

Inclusion Criteria:

• First episode of idiopathic nephrotic syndrome in a child aged 12 months to 18 years with a weight > 10 kg and biologically defined as proteinuria > 0.20 g / mmol creatinuria and hypoalbuminemia <25 g / mmol
• First episode of NIS defined in adults as albumin level <30 g / L and a urinary protein/creatinine ratio (UPCR) ≥ 300 mg / mmol systematically associated with the performance of a renal anatomopathological examination and characterized by the absence of identifiable lesions by light microscopy (SNLGM) or the presence of HSF lesions.
• For adults: signed informed consent to participate in the study
• For children: patients will be informed and a written informed consent form will be signed by both parents of the children at inclusion
• Patients affiliated to the French health system

Exclusion Criteria:

• Patients who have previously received corticosteroids and/or immunosuppressants
• Patients with reduced CH50 and/or low C3 and/or low C4 and/or low C4 (in some cases increased sC5b9 and/or presence of a C3 nephritic Factor; an anti-C3b...)
• SNLGM resulting from a secondary process (lymphoid hematopathies or neoplasia) or occurring following the administration of a treatment known to be associated with an SNLGM (lithium, interferon, non-steroidal anti-inflammatory drugs)
• Non-primary FHH (absence of Nephrotic Syndrome, etiological assessment revealing FHH secondary to an identified cause (genetic or not), no introduction of corticosteroids or immunosuppressants as first-line treatment)
• Positive serological screening test for HIV, hepatitis B or C
• Positive immunological tests for antinuclear and anti-DNA antibodies or anti-PLA2R1 and anti-THSD7A
• Patient under guardianship or curatorship

Study Plan

How is the study designed?

Number of groups / cohorts

2

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
SNLGM; 70 patients with an SNLGM	Other: blood sample; blood sample during planned in the follow-up of patients.; Other: tissue sample; tissue sample during planned in the follow-up of patients.; Other: excreta; urine sample during planned in the follow-up of patients.
primary FSH; 74 with a primary FSH	Other: blood sample; blood sample during planned in the follow-up of patients.; Other: tissue sample; tissue sample during planned in the follow-up of patients.; Other: excreta; urine sample during planned in the follow-up of patients.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
number of biological samples	establish in each centre a prospective collection of blood, urine and kidney biopsy samples sampled and stored in accordance with standard operating procedures, supported by a harmonized clinical and biological database	5 years

Collaborators and Investigators

• Sponsor: Centre Hospitalier Universitaire de Nice

Study record dates

Study Major Dates

• Study Start (Actual): May 20, 2020
• Primary Completion (Anticipated): May 20, 2021
• Study Completion (Anticipated): May 20, 2025

Study Registration Dates

• First Submitted: November 19, 2019
• First Submitted That Met QC Criteria: November 20, 2019
• First Posted (Actual): November 22, 2019

Study Record Updates

• Last Update Posted (Actual): October 19, 2020
• Last Update Submitted That Met QC Criteria: October 15, 2020
• Last Verified: November 1, 2019

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Kidney Diseases; Urologic Diseases; Disease; Syndrome; Nephrotic Syndrome; Nephrosis
• Other Study ID Numbers: 18-PP-16

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No