Literature DB >> 20650534

DFNB1-associated deafness in Portuguese cochlear implant users: prevalence and impact on oral outcome.

Joana Rita Gaspar de Barros Martinho Chora1, Tiago Daniel Morim Matos, Jorge Humberto Ferreira Martins, Marisa Costa Alves, Susana Margarida Sousa Andrade, Luis Filipe dos Santos Silva, Carlos Alberto dos Reis Ribeiro, Marília Cristina de Sousa Antunes, Maria Graça Monteiro Azevedo Fialho, Maria Helena de Figueiredo Ramos Caria.   

Abstract

OBJECTIVES: Hearing loss is a condition that interferes with the development of the child at a cognitive and language level. Therefore, early diagnosis of deafness is important for (re)habilitation, namely through the use of cochlear implant (CI). The present study aimed at screening CI Portuguese individuals for the presence of mutations in the genes GJB2 and GJB6 (DFNB1 locus), and searching a possible correlation between the genotype and the oral habilitation outcome following implantation.
METHODS: Our sample included 117 CI individuals implanted longer than 5 years. Sequencing of GJB2 entire coding region was first performed. The presence of deletions del(GJB6-D13S1830) and del(GJB6-D13S1854) was subsequently tested by multiplex PCR. To assess the oral outcome of these individuals, a global score is calculated through a formula that integrates the results of a battery of speech and audiological tests routinely used in ORL services. This global oral performance score was used to test whether individuals with DFNB1-associated deafness perform significantly better than individuals without DFNB1-associated deafness.
RESULTS: In 35% of the cases, deafness was clearly associated to DFNB1. The most common mutated allele was c.35delG (85%). Other variants have also been found, namely p.Gly130Ala, p.Asn206Ser, p.Val37Ile, p.Glu47X, p.Arg184Trp, p.Trp24X and the two common GJB6 deletions, del(GJB6-D13S1854) and del(GJB6-D13S1830), the last one identified for the first time in our population. Regarding the oral outcome, after testing the homogeneity of the two groups it could be observed that, in mean, the individuals with DFNB1-associated deafness perform significantly better (p=0.012) than the individuals without DFNB1-associated deafness. DISCUSSION AND
CONCLUSION: This first screening of DFNB1 genes in the Portuguese CI population provides clear evidence of the high proportion of DFNB1-associated deafness amongst the Portuguese implanted individuals. DFNB1 status is significantly associated to higher oral performance scores, with DFNB1 individuals performing, on average, 6% better than the individuals without DFNB1-associated deafness.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20650534     DOI: 10.1016/j.ijporl.2010.06.014

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  7 in total

1.  Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesis.

Authors:  Robert W Eppsteiner; A Eliot Shearer; Michael S Hildebrand; Adam P Deluca; Haihong Ji; Camille C Dunn; Elizabeth A Black-Ziegelbein; Thomas L Casavant; Terry A Braun; Todd E Scheetz; Steven E Scherer; Marlan R Hansen; Bruce J Gantz; Richard J H Smith
Journal:  Hear Res       Date:  2012-08-28       Impact factor: 3.208

2.  The effect of GJB2 and SLC26A4 gene mutations on rehabilitative outcomes in pediatric cochlear implant patients.

Authors:  Yu-jun Yan; Yun Li; Tao Yang; Qi Huang; Hao Wu
Journal:  Eur Arch Otorhinolaryngol       Date:  2013-01-08       Impact factor: 2.503

3.  Prevalence of DFNB1 mutations among cochlear implant users in Slovakia and its clinical implications.

Authors:  L Varga; I Mašindová; M Hučková; Z Kabátová; D Gašperíková; I Klimeš; M Profant
Journal:  Eur Arch Otorhinolaryngol       Date:  2013-05-23       Impact factor: 2.503

4.  Speech Perception Outcomes after Cochlear Implantation in Children with GJB2/DFNB1 associated Deafness.

Authors:  Marina Davcheva-Chakar; Emilija Sukarova-Stefanovska; Valentina Ivanovska; Vesna Lazarevska; Ilija Filipche; Beti Zafirovska
Journal:  Balkan Med J       Date:  2014-03-01       Impact factor: 2.021

5.  Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication.

Authors:  Joo Hyun Park; Nayoung K D Kim; Ah Reum Kim; Jihye Rhee; Seung Ha Oh; Ja-Won Koo; Jae-Yong Nam; Woong-Yang Park; Byung Yoon Choi
Journal:  Orphanet J Rare Dis       Date:  2014-11-06       Impact factor: 4.123

6.  Long Term Speech Perception Outcomes of Cochlear Implantation in Gap Junction Protein Beta 2 Related Hearing Loss.

Authors:  Sung Hee Kim; Rajendra Nepali; Myung Hoon Yoo; Kwang-Sun Lee; Jong Woo Chung
Journal:  J Audiol Otol       Date:  2017-07-05

7.  Two portuguese cochlear implanted dizygotic twins: a case report.

Authors:  Joana Rita Chora; Helena Simões-Teixeira; Tiago Daniel Matos; Jorge Humberto Martins; Marisa Alves; Raquel Ferreira; Luís Silva; Carlos Ribeiro; Graça Fialho; Helena Caria
Journal:  Case Rep Genet       Date:  2012-08-23
  7 in total

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