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

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• 作者：Joana Rita Gaspar de Barros Martinho Chora ; Tiago Daniel Morim Matos ; Jorge Humberto Ferreira Martins ; Marisa Costa Alves ; Susana Margarida Sousa Andrade ; Luis Filipe dos Santos Silva ; Carlos Alberto
• 刊名：International Journal of Pediatric Otorhinolaryngology
• 出版年：2010
• 出版时间：October 2010
• 年：2010
• 卷：74
• 期：10
• 页码：1135-1139
• 全文大小：153 K

文摘

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.