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RecruitingNCT07319091CYSTI-MITOUpdated Aug 3, 2026

Cystinosis and Mitochondrial Metabolism

An interventional study of Mitochondrial metabolism in Cystinosis and Native Kidney, sponsored by Hospices Civils de Lyon. Recruiting at 9 sites in France. Open to participants aged 2 Years and older. Per ClinicalTrials.gov, last updated 2026-08-03.

Sponsored by Hospices Civils de Lyon · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
25
Allocation
Not applicable
Ages
2 Years and older
Sex
All
01

Study summary

Cystinosis is a monogenic autosomal recessive lysosomal storage disease with complete penetrance, caused by a biallelic mutation in the CTNS gene (17p13.2) encoding cystinosin, a ubiquitous membrane protein whose role is to clear cystine into the cytosol. Its dysfunction in patients with cystinosis leads to systemic accumulation of cystine, an oxidised dimer of cysteines linked by a disulphide bridge, in the lysosomal space, and irreversible cellular dysfunction. Renal damage is at the forefront, with Fanconi syndrome (proximal tubulopathy) and chronic renal failure developing early in childhood/adolescence. There are also multi-systemic disorders, notably endocrine and ophthalmological. Cysteamine is an amino thiol which reduces the level of intra-lysosomal cystine by breaking the disulphide strands of cystine, giving two cysteines which complex with cysteamine to leave the lysosome. Since the late 1980s, there has been an immediate-release form of the drug, which has considerably improved overall patient survival despite having a major impact on quality of life. This improvement in survival has also led to the emergence of later complications that were not previously observed. This musculoskeletal complication (described in an international consensus in 2019), known as 'CMBD' for Cystinosis Metabolic Bone Disease, may be explained at least in part by an intrinsic defect in the osteoblast and osteoclast that contribute to the human bone phenotype. This intrinsic bone defect appears to be responsible for premature ageing. In order to identify potential future therapeutic targets for CMBD, it is essential to gain a better understanding of the underlying pathophysiological mechanisms.

To better understand premature aging in extra-renal damage in cystinosis, it seems relevant to investigate energy metabolism dysfunction, particularly mitochondrial dysfunction.

02

Conditions studied

  • Cystinosis
  • Native Kidney

Keywords

  • Cystinosis
  • Mitochondria
  • Cystinosis Metabolic Bone Disease (CMBD)
  • Myopathy
03

Who can participate

Ages eligible
2 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patient with genetically confirmed nephropathic cystinosis
  • Men and women, children and adults with cystinosis
  • Undergoing conservative treatment on native kidneys
  • Age ≥ 2 years
  • Patients receiving oral cysteamine
  • Patients with social security coverage
  • Informed consent signed by the participant or parents or legal guardians before participating in the study

Exclusion criteria

Exclusion Criteria:

  • Patient not complying with study procedures
  • Transplant or dialysis patient
  • Patient on anticalcineurin
  • Pregnant or breast-feeding woman
  • Person deprived of liberty by a judicial or administrative decision
  • Person not affiliated to a social security scheme or beneficiaries of a similar scheme
04

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
25 participants (estimated)

Study arms

  • Other
    Cystinosis patient

    Patient with genetically confirmed nephropathic cystinosis Men and women, children and adults with cystinosis Undergoing conservative treatment on native kidneys Age ≥ 2 years Patients receiving oral cysteamine Patients with social security coverage Informed consent signed by the participant or parents or legal guardians before participating in the study

    Other: Mitochondrial metabolism

Interventions

  • OtherMitochondrial metabolism

    Study of membrane potential by flow cytometry of circulating monocyte cells and evaluate the respiratory chain of these cells in patients with cystinosis and described musculoskeletal disorders in the study population in clinical and biological terms including metabolomic analysis of patients' blood and urine

05

What researchers measure

Primary outcomes

  1. Membrane potential of circulating monocyte cells

    Mitochondrial metabolism was assessed by measuring the membrane potential by flow cytometry of circulating monocyte cells between subjects with and without cystinosis.

    Time frame: 24 months

Secondary outcomes

  1. Oxygen consumption rate (OCR) of circulating monocytic cells

    The oxygen consumption rate (OCR) of circulating monocytic cells is measured by the Seahorse method. This method also measures the extracellular acidification rate (ECAR) of cells. The oxygen consumption rate (OCR) and the extracellular acidification rate (ECAR) are used to assess the respiratory chain of the cells, which will be compared between subjects with and without cystinosis.

    Time frame: 24 months

  2. Extracellular acidification rate (ECAR) of circulating monocytic cells

    The extracellular acidification rate (ECAR) of circulating monocytic cells is measured by the Seahorse method. This method also measures the oxygen consumption rate (OCR) of cells. The extracellular acidification rate (ECAR) and the oxygen consumption rate (OCR) are used to assess the respiratory chain of the cells, which will be compared between subjects with and without cystinosis.

    Time frame: 24 months

  3. Age

    The patient's age is a data used to produce a clinical description of musculoskeletal disorders based on current practice data such as : sex, weight, height, blood pressure, treatment, bone deformity, clinical sign of myopathy, grip strength test using the Grip-test (Z score) and the EAT10 (Eating Assessment Tool) questionnaire

    Time frame: 24 months

  4. Sex

    The patient's sex is a data used to produce a clinical description of musculoskeletal disorders based on current practice data such as : age, weight, height, blood pressure, treatment, bone deformity, clinical sign of myopathy, grip strength test using the Grip-test (Z score) and the EAT10 (Eating Assessment Tool) questionnaire

    Time frame: 24 months

  5. Weight

    The patient's weight is a data used to produce a clinical description of musculoskeletal disorders based on current practice data such as : age, sex, height, blood pressure, treatment, bone deformity, clinical sign of myopathy, grip strength test using the Grip-test (Z score) and the EAT10 (Eating Assessment Tool) questionnaire

    Time frame: 24 months

  6. Height

    The patient's height is a data used to produce a clinical description of musculoskeletal disorders based on current practice data such as : age, sex, weight, blood pressure, treatment, bone deformity, clinical sign of myopathy, grip strength test using the Grip-test (Z score) and the EAT10 (Eating Assessment Tool) questionnaire

    Time frame: 24 months

  7. Blood pressure

    The patient's blood pressure is a data used to produce a clinical description of musculoskeletal disorders based on current practice data such as : age, sex, weight, height, treatment, bone deformity, clinical sign of myopathy, grip strength test using the Grip-test (Z score) and the EAT10 (Eating Assessment Tool) questionnaire

    Time frame: 24 months

  8. Type of treatment

    The patient's type of treatment is a data used to produce a clinical description of musculoskeletal disorders based on current practice data such as : age, sex, weight, height, blood pressure, bone deformity, clinical sign of myopathy, grip strength test using the Grip-test (Z score) and the EAT10 (Eating Assessment Tool) questionnaire

    Time frame: 24 months

  9. Bone deformity

    The patient's bone deformity is a data used to produce a clinical description of musculoskeletal disorders based on current practice data such as : age, sex, weight, height, blood pressure, treatment, clinical sign of myopathy, grip strength test using the Grip-test (Z score) and the EAT10 (Eating Assessment Tool) questionnaire

    Time frame: 24 months

  10. Clinical sign of myopathy

    Clinical sign of myopathy is a data used to produce a clinical description of musculoskeletal disorders based on current practice data such as : age, sex, weight, height, blood pressure, treatment, bone deformity, grip strength test using the Grip-test (Z score) and the EAT10 (Eating Assessment Tool) questionnaire

    Time frame: 24 months

  11. Grip-test score

    The Grip-test is used to assess grip strength. Grip-test score is a data used to produce a clinical description of musculoskeletal disorders based on current practice data such as : age, sex, weight, height, blood pressure, treatment, bone deformity, clinical sign of myopathy and the EAT10 (Eating Assessment Tool) questionnaire

    Time frame: 24 months

  12. EAT10 (Eating Assessment Tool) questionnaire score

    EAT10 (Eating Assessment Tool) questionnaire score is pathological if \>= 3 : * 3-10 mild dysphagia * 11-20 moderate dysphagia * 21-40 severe dysphagia) questionnaire. EAT10 score is a data used to produce a clinical description of musculoskeletal disorders based on current practice data such as : age, sex, weight, height, blood pressure, treatment, bone deformity, clinical sign of myopathy and grip-test score

    Time frame: 24 months

  13. Complete ionogram

    Complete ionogram is a data used to produce biological description of musculoskeletal disorders based on routine practice data such as C-reactive protein (CRP), intra-leukocyte cystine, Parathyroid hormone (PTH), total alkaline phosphatases, 25(OH) vitamin D, 1-25 (OH) vitamin D

    Time frame: 24 months

  14. C-Reactive Protein (CRP)

    C-Reactive Protein (CRP) is a data used to produce biological description of musculoskeletal disorders based on routine practice data such as complete ionogram, intra-leukocyte cystine, Parathyroid hormone (PTH), total alkaline phosphatases, 25(OH) vitamin D, 1-25 (OH) vitamin D

    Time frame: 24 months

  15. Intra-leukocyte cystine

    Intra-leukocyte cystine is a data used to produce biological description of musculoskeletal disorders based on routine practice data such as complete ionogram, C-Reactive Protein (CRP), Parathyroid hormone (PTH), total alkaline phosphatases, 25(OH) vitamin D, 1-25 (OH) vitamin D

    Time frame: 24 months

  16. Parathyroid hormone (PTH)

    Parathyroid hormone (PTH) is a data used to produce biological description of musculoskeletal disorders based on routine practice data such as complete ionogram, C-Reactive Protein (CRP),intra-leukocyte cystine, total alkaline phosphatases, 25(OH) vitamin D, 1-25 (OH) vitamin D

    Time frame: 24 months

  17. Total alkaline phosphatases

    Total alkaline phosphatases is a data used to produce biological description of musculoskeletal disorders based on routine practice data such as complete ionogram, C-Reactive Protein (CRP), intra-leukocyte cystine, Parathyroid hormone (PTH), 25(OH) vitamin D, 1-25 (OH) vitamin D

    Time frame: 24 months

  18. 25(OH) vitamin D

    25(OH) vitamin D is a data used to produce biological description of musculoskeletal disorders based on routine practice data such as complete ionogram, C-Reactive Protein (CRP), intra-leukocyte cystine, Parathyroid hormone (PTH), total alkaline phosphatases, 1-25 (OH) vitamin D

    Time frame: 24 months

  19. 1-25 (OH) vitamin D

    1-25 (OH) vitamin D is a data used to produce biological description of musculoskeletal disorders based on routine practice data such as complete ionogram, C-Reactive Protein (CRP), intra-leukocyte cystine, Parathyroid hormone (PTH), total alkaline phosphatases, 25 (OH) vitamin D

    Time frame: 24 months

  20. Distribution of plasma organic amino acids

    Study of metabolomic analysis of patients' blood

    Time frame: 24 months

  21. Distribution of urinary organic amino acids

    Study of metabolomic analysis of patients' urine

    Time frame: 24 months

  22. Urinary Krebs cycle intermediate metabolites

    Study of metabolomic analysis of patients' urine

    Time frame: 24 months

  23. Membrane potential of circulating monocyte cells from patients treated with selenium

    Mitochondrial metabolism was assessed by measuring the membrane potential by flow cytometry of circulating monocyte cells from patients with cystinosis treated with selenium

    Time frame: 30 months

06

Study locations

9 of 9 sites recruiting
  • Service de néphrologie pédiatrique, Hôpital Femme Mère Enfant, Hospices Civils de Lyon
    Bron, 69677 Bron Cedex, France
    • Justine BACCHETTA, MD · Contact · justine.bacchetta@chu-lyon.fr · 4 27 85 61 30
    • Justine BACCHETTA, MD · Principal investigator
    • Chloé GROSYEUX, MD · Sub investigator
    • Aurélia BERTHOLET-THOMAS · Sub investigator
    Recruiting
  • Service de Néphrologie pédiatrique, Hôpital Jeanne de Flandre
    Lille, 59000, France
    • Robert NOVO, MD · Contact
    • Robert NOVO, MD · Principal investigator
    Recruiting
  • Service de néphrologie et exploration fonctionnelle rénale, Hôpital Edouard Herriot, Hospices Civils de Lyon
    Lyon, 69003, France
    • Sandrine LEMOINE, MD · Contact
    • Sandrine LEMOINE, MD · Principal investigator
    Recruiting
  • Service de Néphrologie pédiatrique, Hôpital de la Timone
    Marseille, 13385, France
    • Caroline ROUSSET-ROUVIERE, MD · Contact
    • Caroline ROUSSET-ROUVIERE, MD · Principal investigator
    Recruiting
  • Service de Néphologie et endocrinologie pédiatrique, Hôpital Arnaud de Villeneuve
    Montpellier, 34295, France
    • Marc FILA, MD · Contact
    • Marc FILA, MD · Principal investigator
    Recruiting
  • Service de Néphrologie pédiatrique, Hôpital Necker-Enfants Malades
    Paris, 75015, France
    • Olivia BOYER, MD · Contact
    • Olivia BOYER, MD · Principal investigator
    Recruiting
  • Service de Néphrologie-transplantation rénale adultes, Hôpital Necker-Enfants Malades
    Paris, 75015, France
    • Aude SERVAIS, MD · Contact
    • Aude SERVAIS, MD · Principal investigator
    Recruiting
  • Service de Néphrologie pédiatrique, Hôpital Robert Debré
    Paris, 75019, France
    • Julien HOGAN, MD · Contact
    • Julien HOGAN, MD · Principal investigator
    Recruiting
  • Service de Néphrologie-Dialyse-Transplantation pédiatrique, Hôpital d'enfants Brabois
    Vandœuvre-lès-Nancy, 54511, France
    • Isabelle VRILLON, MD · Contact
    • Isabelle VRILLON, MD · Principal investigator
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07319091
Lead sponsor
Hospices Civils de Lyon
Responsible party
Sponsor
First posted
Jan 6, 2026
Start date
Dec 8, 2025
Primary completion
Dec 2027 (estimated)
Completion
Jul 2028 (estimated)
Last update
Aug 3, 2026

Study contacts

Justine BACCHETTA, MD
Contact
justine.bacchetta@chu-lyon.fr
4 27 85 61 30 ext. +33
Chloé GROSYEUX, MD
Contact
chloe.grosyeux@gmail.com

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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