Renal and Vascular Phenotypic Characterization of Patients With Enamel Renal Syndrome Due to a Pathogenic Variant of the FAM20A Gene and Pathophysiological Study of Ectopic Calcifications
NCT07285421 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2025-12-16
Summary
In the research, the investigators will characterize the renal and vascular damage and look for factors favoring the formation of calcification induced by enamel renal syndrome.
Patients will undergo four investigations, as part of their routine care, to assess their renal impairment. Each investigation will require a day in the Physiology Department of the George Pompidou European Hospital.
The 4 tests are designed to
* precisely measure your renal filtration capacity,
* evaluate your body's calcium and phosphate regulation,
* evaluate your capacity to regulate the elimination of water from the body
* assess your body's ability to regulate "acid" intake. As part of the research, an additional 20 ml blood sample and a urine sample will be taken during the other samples taken as part of routine care.
Healthy volunteers will undergo blood and urine tests, dental X-rays and renal ultrasound. For healthy volunteers, the aim of the dental X-ray and renal ultrasound is to check that there are no dental or renal abnormalities, so as to rule out not only email-rein syndrome, but also any dental or renal abnormalities that might resemble it. The aim of blood and urine sampling is to measure various molecules that promote calcification or inhibit the calcification process, so as to be able to compare results obtained in healthy subjects with those obtained in patients with enamel renal syndrome. Each healthy subject will be selected to be matched by age and sex to each of the patients included in the study.
Conditions
- Enamel Renal Syndrome
Interventions
- DIAGNOSTIC_TEST
-
urinary proteome
Volume 2 ml, with protease inhibitor made one time for each arm of the protocol
- DIAGNOSTIC_TEST
-
urinary metabolome
Sample collected once in the protocol for each arm.
- DIAGNOSTIC_TEST
-
Evaluation of plasma mineralization factors
Complementary plasma analysis during another blood sample collection for both arms
- DIAGNOSTIC_TEST
-
Renal ultrasound
Verification of normal renal morphology, absence of nephrocalcinosis
- RADIATION
-
dental panoramic x-ray
Verification of normal dentition
- BIOLOGICAL
-
Blood and urine minimal biology
Fasting blood: creatinine, blood ions (Na + K + Cl + CO2 + Proteins), calcium, phosphate, CBC (Complete Blood Count), liver function tests, lipid profile); Morning fasting urine: creatinine, calcium, phosphate, protein, urinalysis (ECBU)
Sponsors & Collaborators
-
Fondation Université de Paris
collaborator UNKNOWN -
Université de Liège
collaborator OTHER -
Institut Necker Enfants Malades
collaborator OTHER -
Assistance Publique - Hôpitaux de Paris
lead OTHER
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2026-01-01
- Primary Completion
- 2029-10-30
- Completion
- 2029-10-30
Countries
- France
Study Locations
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