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

被引:16
作者
de Barros Martinho Chora, Joana Rita Gaspar [1 ]
Morim Matos, Tiago Daniel [1 ]
Ferreira Martins, Jorge Humberto [2 ]
Alves, Marisa Costa [2 ]
Sousa Andrade, Susana Margarida [2 ]
dos Santos Silva, Luis Filipe [2 ]
dos Reis Ribeiro, Carlos Alberto [2 ]
de Sousa Antunes, Marilia Cristina [3 ]
Monteiro Azevedo Fialho, Maria Graca [1 ]
de Figueiredo Ramos Caria, Maria Helena [1 ,4 ]
机构
[1] Univ Lisbon, Fac Sci, Ctr Biodivers Funct & Integrat Genom, BioFIG, P-1749016 Lisbon, Portugal
[2] Ctr Hosp Coimbra, ENT Dept, P-3041801 Coimbra, Portugal
[3] Univ Lisbon, Fac Sci, Ctr Stat & Applicat, P-1749016 Lisbon, Portugal
[4] Polytech Inst Setubal, Higher Coll Hlth, P-2910470 Setubal, Portugal
关键词
DFNB1; deafness; GJB2; mutations; GJB6; deletions; Oral rehabilitation; Cochlear implant outcome; HEARING-LOSS; MUTATIONS; GENE;
D O I
10.1016/j.ijporl.2010.06.014
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
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 (Cl). 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.Val37lle, 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. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1135 / 1139
页数:5
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