Official Title
The FOrMe Registry (The German Focal Segmental Glomerulosclerosis and Minimal Change Disease Registry)
Brief Title
The FOrMe Registry (The German Focal Segmental Glomerulosclerosis and Minimal Change Disease Registry)
Protocol ID
NCT03949972
Lead Sponsor
Prof. Dr. Paul Brinkkoetter
Brief Summary
In a monocentric, later multicentric prospective approach the FOrMe registry (The German
Focal Segmental Glomerulosclerosis and Minimal Change Disease Registry) aims to generate
a longitudinal cohort of 150 pediatric cases of idiopathic nephrotic syndrome and 350
adult cases of biopsy-proven Minimal Change Disease (MCD) or Focal and Segmental
Glomerular Sclerosis (FSGS) over 10 years. The registry will provide a repository for
biomaterials such as blood samples, DNA, urine, feces, and tissue biopsies that will be
accessible to collaborators to facilitate future research on pathogenesis, diagnostics,
and treatment.
Detailed Description
Idiopathic Nephrotic Syndrome is characterized by proteinuria, volume retention,
hyperlipidemia, hypoalbuminemia. As Minimal Change Disease (MCD) represents by far the
most prevalent underlying diagnosis in children older than 1 year, a kidney biopsy is
usually deferred in these cases. In adolescence and adults, a kidney biopsy is crucial
for the diagnosis because MCD and FSGS account for only 10-15 and 12-35 percent of all
cases of nephrotic syndrome respectively. Pathomechanisms as well as optimal treatment
remain elusive as systematic trials are scarce and hampered by low incidence and
heterogenicity of the clinical presentation. To bridge this informational gap, the
investigators identified the need for a German registry of pediatric and adult patients
with idiopathic nephrotic syndrome (in children) and biopsy-proven MCD/FSGS (in adults).
The registry will record clinical data of participants regarding basic demographics,
initial presentation, hereditary traits, disease course and treatment modalities as well
as quality of life, concomitant diseases, and comedication. During the initial visit and
to a lesser intent on follow-up visits, biomaterials (blood, urine, DNA, feces, tissue)
will be collected and stored in a state-of-the art biobank. This material will be
available to collaborators to support research on idiopathic nephrotic syndrome and
MCD/FSGS. By the time of completion, the registry will provide data on clinical courses
and outcome of approximately 500 patients that can easily be correlated with biomaterials
giving insight into risk factors, prognostic parameters, and association with
comorbidities.
Tissue sections of all patients that undergo kidney biopsy (all adult and some pediatric
patients) will be digitalized, annotated, and analyzed by a panel of nephropathologists.
Histopathologic features will be individually assessed and scored according to a set of
descriptors that was developed and is used by the American NEPTUNE (Nephrotic Syndrome
Study Network).
Study Period
-
Enrollment Count
500 participants
Eligibility Criteria
Inclusion Criteria (cohort A):
- written informed consent
- 17 or less years of age
- idiopathic nephrotic syndrome
Inclusion Criteria (cohort B):
- written informed consent
- older or equal to 18 years of age
- biopsy-proven primary or secondary FSGS or MCD or biopsy-proven recurrence of
disease in kidney transplant.
Exclusion Criteria (both cohorts):
- Prior kidney transplant without biopsy-proven recurrence
- A clinical diagnosis of other glomerular disease resulting in secondary MCD or FSGS
as judged by the treating physicians.
- Refusal to provide written informed consent
- (Anticipated) incompliance with visit schedule
Filters
Glomerulosclerosis, Focal Segmental
Minimal Change Disease
Idiopathic Nephrotic Syndrome
RECRUITING
CHILD
ADULT
OLDER_ADULT