Generation of a Cellular Model of CADASIL From Skin Fibroblasts

Sponsor
Institut National de la Santé Et de la Recherche Médicale, France (Other)
Overall Status
Unknown status
CT.gov ID
NCT02032225
Collaborator
(none)
10
1
53.9
0.2

Study Details

Study Description

Brief Summary

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy (CADASIL) is an archetypal small vessel disease of the brain caused by dominant mutations in the NOTCH3 receptor. Cardinal vascular lesions include deposition of granular osmiophilic material (GOM) within the basal lamina of smooth muscle cells, progressive smooth muscle cell loss, and fibrosis of the media. Pathogenic mutations alter the number of cysteine residues in the extracellular domain of NOTCH3 (Notch3 ECD), leading to its abnormal accumulation in the GOM deposits. Vascular smooth muscle cell has been identified as the primary target cell in this disease. Pathophysiological processes leading from NOTCH3 mutations to smooth muscle cell loss remain poorly understood.

The investigators propose to study these mechanisms by reprogramming skin cells to become stem cells and then differentiating them to vascular smooth muscle cells.

The hypothesis of this study is that the differentiated smooth muscle cells will display the characteristic features of CADASIL, ie, Notch3 ECD accumulation and GOM deposits.

Condition or Disease Intervention/Treatment Phase
  • Other: Skin biopsy

Study Design

Study Type:
Observational
Anticipated Enrollment :
10 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Obtention d'un modèle Cellulaire de la Maladie CADASIL à Partir de Fibroblastes cutanés de Patients
Study Start Date :
Feb 1, 2014
Anticipated Primary Completion Date :
Aug 1, 2018
Anticipated Study Completion Date :
Aug 1, 2018

Arms and Interventions

Arm Intervention/Treatment
CADASIL

patients with CADASIL

Other: Skin biopsy

Outcome Measures

Primary Outcome Measures

  1. Derivation of iPS cells from skin biopsies of patients with CADASIL [30 months]

Secondary Outcome Measures

  1. Differentiation of iPS cells to vascular smooth muscle cells, phenotypic and mechanistic analyses [24 mois]

    Differentiation of iPS cells to vascular smooth muscle cells and phenotypic analysis (12 mois) Mechanistic analyses (12 mois)

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria :
  • Between 30 and 60 years;

  • Having a social security scheme or, CMU ;

  • Diagnosis of CADASIL confirmed by molecular analysis performed previously (missense mutation in the Notch3 gene affecting the number of cysteine in one of the 34 EGFR of NOTCH3 ) ;

  • No countra-indication for a skin biopsy (ongoing treatment with anti-coagulant, history of bleeding disorder or deficiency of blood clotting factors) ;

  • Written consent given.

Exclusion Criteria :
  • Patients without social security scheme or, CMU ;

  • Patients aged under 30 or over 60 years at the time of the first visit ;

  • Pregnant women beyond the 5th month of pregnancy

  • Patients who are not able to give informed consent ;

  • Countra-indication to the achievement of the skin biopsy ( ongoing treatment with anti- coagulant, history of bleeding disorder or deficiency of coagulation factors ) .

Contacts and Locations

Locations

Site City State Country Postal Code
1 INSERM Paris France 75010

Sponsors and Collaborators

  • Institut National de la Santé Et de la Recherche Médicale, France

Investigators

  • Principal Investigator: Anne JOUTEL, MD, PhD, Institut National de la Santé Et de la Recherche Médicale, France

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Institut National de la Santé Et de la Recherche Médicale, France
ClinicalTrials.gov Identifier:
NCT02032225
Other Study ID Numbers:
  • C13-34
  • 2013-A00994-41
First Posted:
Jan 9, 2014
Last Update Posted:
Dec 7, 2016
Last Verified:
Dec 1, 2016
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 7, 2016