Biocollection on the Familial Forms of Intracranial Aneurysm (GAÏA)

Nantes University Hospital (NUH)

Status: Completed

Conditions: Intracranial Aneurysm

Treatments: Genetic: Non-Interventional

Study type: Observational

Funder types: Other

Identifiers

NCT02848495

RC12_0458

Details and patient eligibility

About

Intracranial aneurysm (IA) is an asymptomatic cerebrovascular abnormality affecting 3.2% of the general population. The devastating complication of IA is its rupture, resulting in subarachnoid haemorrhage that can lead to severe disability and death.

Unfortunately, there are neither reliable clues nor diagnostic tools to predict the formation and/or the fate of an IA in a given individual. Also, there is no pharmacological drug available to prevent the rupture of aneurysm and subsequent subarachnoid haemorrhage. Current treatments are invasive with a significant risk of procedural morbidity. Thus, still now, the management of patients with IA remains extremely challenging and still controversial.

Although the pathogenesis of IA has been the subject of many studies for the last decade, the mechanisms underlying IA formation, growth and rupture are still mostly unknown and relevant animal models of IA are not available.

Familial history of IA predisposes to IA formation and rupture and increasing evidence suggest a genetic component of IA formation, with heterogeneous modes of inheritance and penetrance.

This project, gathering neuroradiologists, geneticists and vascular biologists, addresses the urgent need to understand the pathogenic mechanisms of IA to develop diagnostic and predictive tools of risk of IA.

The investigators propose to identify IA-causing variants by whole-exome sequencing in familial forms of the disease.

The investigators hypothesises that the functional analysis of the causal / susceptibility variants thus identified will provide clues to understanding the pathological mechanisms of IA formation, and the bases for developing diagnostic tools. This project aims at meeting this challenge. Based on preliminary data that already allowed to identify such a variant, and the combination of genetic and functional investigations, the specific objectives of this project are: - To identify IA-causing variants in familial forms of the disease by whole-exome sequencing; - To understand the function of these genes/ variants in the formation and rupture of IA by molecular and cellular approaches and generation of relevant animal models; - To discover potential biomarkers of risk of IA formation and/or rupture.

Enrollment: 411 patients

Sex: All

Ages: 20+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria :

• Inclusion criteria indexes and related cases (familial) of intracranial aneurysms:

  • Index: Any patient consulting for a major IA and some typical bifurcation with at least one other case reached akin IA 1st degree
  • Related: All similar to the first degree, aged 20 or more, patients with a family background of IA and some typical bifurcation (≥2 achieved) For the latter, directed by screening with Magnetic resonance imaging (MRI) sequence Time of Flight (TOF), axial T2, EGT2.
  • Consent oral and in writing to the Biocollection consent Form for participation in the collection of biological samples

• Inclusion criteria sporadic cases of IA:

  • Any patient consulting for IA and some typical bifurcation
  • Patients aged of 20 years or older
  • Consent oral and in writing to the Biocollection consent Form for participation in the collection of biological samples

Exclusion Criteria :

• Non Inclusion Criteria:

• Patients who have shown the inability or have refused to sign the consent informed biocollection
• Syndromic diagnosis known as IA provider
• Marfan Syndrome
• AOS with SMAD 3
• Danlos Syndrome Elhers type II and IV
• Autosomal Dominant Polycystic
• Moyamoya Syndrome
• Character of IA:
• Dissecting or fusiform
• Combined with an arteriovenous malformation
• Blister-like
• Mycotic
• Pathology of the cerebral white matter detected on MRI, evoking:
• COL4A1 mutation