Nephropathic Cystinosis
Conditions
Brief summary
Nephropathic Cystinosis (NC) is an orphan inherited autosomal recessive disease characterised as a generalized lysosomal storage disease due to a deficiency of the cystine lysosomal transport protein, cystinosin. Patients with NC usually receive cysteamine. Bone impairment was recently recognized as a late complication of NC, occurring at adolescence or early adulthood. Even though the exact underlying pathophysiology is unclear, at least six hypotheses are discussed, and mainly cysteamine toxicity and/or direct bone effect of the Cystinosin (CTNS) mutation. Because of the potential dramatic impact on quality of life of this novel complication, research should aim to better understand bone disease in NC. The primary objective of this study is to evaluate the action of cysteamine on osteoclastic differentiation and resorption activity of NC patients, depending on the underlying genotype. The Secondary objective is to describe the clinical bone status of NC patients depending on their underlying genotype.
Interventions
OTHERBlood sampling
25 mL blood sample will be collected on citrate tubes for osteoclastic analysis.
Sponsors
Hospices Civils de Lyon
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
2 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Male and female subjects with confirmed diagnosis of nephropathic cystinosis (defined by clinical signs, White Blood Cells (WBC) cystine level and/or mutation), currently receiving oral cysteamine. * Age \> 2 years. * Subjects and/or their parents/ legal guardian must provide non opposition prior to participation in the study.
Exclusion criteria
* Subjects who, in the opinion of the Investigator, are not able or willing to comply with the protocol.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of positive Tartrate-resistant acid phosphatase (TRAP) cells | 1 day | Number of positive TRAP cells will be assessed at the end of osteoclast differentiation from circulating monocytes |
Countries
France, Germany, Italy, Turkey (Türkiye)
Contacts
Primary ContactJustine BACCHETTA, MD PhD
Backup ContactSegolene GAILLARD
Outcome results
None listed