Prevalence of POU4F3 and SLC17A8 Mutations

NCT ID: NCT01802190

Last Updated: 2015-07-21

Basic Information

• Recruitment Status: TERMINATED
• Total Enrollment: 50 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2011-03-31
• Study Completion Date: 2014-09-30

Brief Summary

The study will allow to identify the prevalence of the SLC17A8 gene mutations in patients suffering from deafness. This phenotype also corresponds to DFNA15 deafness caused by POU4F3 : mutations of this gene will be screened as well.

Detailed Description

DFNA are characterized as progressive bilateral deafness. To date, 21 genes and 57 loci are involved in these dominant deafness, with an unknown prevalence.A 22nd gene responsible of the disease has been found. This SLC17A8 gene encodes for the VGLUT3 protein which is specifically expressed in sensorial cells of the audition. VGlut3-/- mice present a deep deafness due to a deficiency of neurotransmitter release, although sensorial cells and neurons are intact. This kind of deafness is an ideal candidate for a genetic therapy because of the cells integrity.Mutations of SLC17A8 gene have been found in 2 american families that suffer from progressive deafness.The study aims to look for european families from the Mediterranean basin, which carry SLC17A8 gene mutations, and may benefit in a medium-term from genetic therapy. The study will allow to identify the prevalence of the SLC17A8 gene mutations in patients suffering from deafness. This phenotype also corresponds to DFNA15 deafness caused by POU4F3 : mutations of this gene will be screened as well.

Conditions

Familial Deafness

Study Design

• Study Time Perspective: PROSPECTIVE

Study Groups

Deafness patients

Deafness patients

Deafness patients

Intervention Type: GENETIC

SLC17A8 et POU4F3 mutations genes analysis on blood samples of deafness patients.

Interventions

Deafness patients

SLC17A8 et POU4F3 mutations genes analysis on blood samples of deafness patients.

Intervention Type: GENETIC

Other Intervention Names

SLC17A8 et POU4F3 mutations genes analysis

Eligibility Criteria

Inclusion Criteria

• Age > 18 years
• Patients with a

1. suggestive neurosensory Deafness: The characteristics of the deafness will be determined from the data of the questionnaire, of the interrogation, the examination and results of the tonal audiometry.

*Neurosensory deafness: Audiometrics measurement(difference between the tonal audiometric average loss for the frequencies 0,5, 1, 2 and 4 kHz in air conduction and in osseous conduction) < 15 dB for each of both ears.

• Bilateral symetric: difference between the audiometric thresholds of both ears < or = 15 dB for at least two frequencies.
• Light to severe: The degree of deafness is defined according to the following classification (moderate hearing loss calculated on the frequencies 500 Hz, 1, 2 and 4 kHz): light hearing deficiency from 20 to 40 dB, moderate hearing deficiency of 40 to 70 dB, severe hearing deficiency of 70 in 90 dB and deep hearing deficiency beyond 90 dB.
• Whose thresholds frequency by frequency in tonal audiometry (air conduction) are superior to the thresholds of the 90th percentile of the standard ISO 7029.
• Without environmental exposition factors.

2. Dominant autosomal transmission diagnosed from one of the following elements:

• Deafness at a father and his son
• Deafness at a father and his daughter outside a suggestive context of a dominant form X-related. (deep deafness at the father and light to moderate deafness in daughter)
• Deafness at a mother and her daughter
• Deafness at a mother and her son outside a suggestive context of a dominant X-related(light to moderate deafness at the mother, and deep deafness at the son)
• Deafness at a patient whose a dead parent had a sure or likely deafness according to the criteria of diagnosis mentioned previously

3. given the consent to participate at this clinical study

Exclusion Criteria

• Suggestive symptom of a polymalformative syndrom
• familial Consanguinity
• Age < 18 years
• Deafness of transmission or mixed
• Deafness of asymmetric or fluctuating perception
• Prelingual deep Deafness
• Pathology of the ear (otospongiose, disease of Ménière, neurinome of the acoustics)

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Montpellier

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Michel MONDAIN, PU-PH

Role: PRINCIPAL_INVESTIGATOR

CHRU Montpellier

Locations

Mondain Michel

Montpellier, , France

Countries

France

Other Identifiers

2010-A00561-38

Identifier Type: OTHER

Identifier Source: secondary_id

8640

Identifier Type: -

Identifier Source: org_study_id