Better Delineation of DDX3X Related Phenotype and Epigenetic Signature.

NCT ID: NCT04436588

Last Updated: 2020-06-18

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 10 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2019-11-01
• Study Completion Date: 2020-12-01

Brief Summary

DDX3X related disorder is mainly characterised by developmental delay (DD) and intellectual disability (ID), ranging from mild to severe, and neuroimaging abnormalities.

The aims of this study are first to better delineate the clinical phenotype, as well as the neuropsychological profile and, second, to study the epigenetic signature in a cohort of individuals with DDX3X pathogenic variants. This work will conduct to a MD thesis of a clinical resident geneticist in France.

Physician that will participate will fill an Excel sheet regarding the clinical and neuropsychological assessment. The investigators will be also happy to have a DNA sample with a minimum 0.5ug of peripheral blood genomic DNA. The investigators will gather the DNA in Montpellier genetic lab (Dr Mouna BARAT) and send the batch to the Dr Sadikovic' lab.

Between 2018 and 2020, the investigators have already recruited data from individuals with DDX3X pathogenic variants from several European and Asian genetic centres

Detailed Description

The investigators aim to better understand and delineate the genetic syndrome DDX3X.

This genetic disorder was described in 2015 by Lot Snijders Blok et al. (DOI https://doi.org/10.1016/j.ajhg.2015.07.004:).

Since this first publication of 38 female individuals carrying a pathogenic mutation DDX3X, 15 more individuals have been reported.

The investigators are seeking to better define the phenotype of individuals with pathogenic variants of DDX3X, to better understand intellectual functioning as well as the strengths and weaknesses of intellectual functioning by collecting standardized neuropsychological assessments already performed such as WPPSI/WISC and WAIS. For this purpose, the investigators will gather clinical and neuropsychological data already carried out in the context of care.

Finally, the investigators will attempt to identify an epigenetic signature in this genetic disease. To this end, the investigators will collect genomic DNA from peripheral blood already collected for genetic analysis and send an anonymized batch of samples to our collaborator, Dr. Bekim Sadicovik. Dr. Bekim Sadicovik and his team will compare the epigenetic DNA methylation-type markers with the corresponding sex and age controls. If specific probes are abnormally methylated in DDX3X individuals, this will determine a disease-specific epigenetic signature. The investigators will then be able to propose an epigenetic signature for individuals with uncharacterized DDX3X variations (class 3, VUS). This method will make it possible to define whether the variation is responsible for the disease or not without going through functional analysis steps that are difficult to implement routinely.

The expected benefits are a better understanding of DDX3X disease, keys to neuropsychological rehabilitation, a better understanding of human brain functions, the possibility of proposing an epigenetic signature for people in whom it is not possible to decide whether a variation in the DDX3X gene is pathological or not

Conditions

Intellectual Developmental Disorder; X-LINKED

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: OTHER

Study Groups

DDX3X

DDX3X

Epigenetic signatures

Intervention Type: GENETIC

Epigenetic signatures (Dr Sadikovic' lab, London, Ontario, Canada)

Interventions

Epigenetic signatures

Epigenetic signatures (Dr Sadikovic' lab, London, Ontario, Canada)

Intervention Type: GENETIC

Eligibility Criteria

Inclusion Criteria

• DDX3X pathogenic Variant

Exclusion Criteria

• no pathogenic variant in DDX3X
• no consent for the study

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Association Xtraordinaire sub-group DDX3X

UNKNOWN

Sponsor Role: collaborator

Genida

UNKNOWN

Sponsor Role: collaborator

University Hospital, Montpellier

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

David GENEVIEVE

Role: PRINCIPAL_INVESTIGATOR

Department of Medical Genetics

Locations

UH Montpellier

Montpellier, , France

Countries

France

Other Identifiers

RECHMPL20_0353

Identifier Type: -

Identifier Source: org_study_id