Genetic susceptibility to noise induced hearing (oss(NIHL)) / Susceptibilidade genética à perda auditiva induzida por ruído (PAIR)

AUTOR(ES)
DATA DE PUBLICAÇÃO

2008

RESUMO

Chronic exposure to loud noise is the most important environmental cause of hearing impairment among adults. Chronic and irreversible hearing loss due to exposure to noise is named Noise Induced Hearing Loss (NIHL). The aim of this study was to investigate the influence of genetic factors in the susceptibility to NIHL. We compared individuals with and without NIHL regarding ethnic origin, familial history of hearing loss, age, noise exposure time, alcohol consumption and smoking habits. In order to investigate genetic factors associated to NIHL we screened frequent deafness causative mutations. The investigated mutations were 35delG and 167delT in the GJB2 gene, Δ(GJB6- D13S1830) and Δ(GJB6- D13S1854) in the GJB6 gene and A1555G in the MT-RNR1 gene. Allelic and genotypic frequencies were determined for the SNP RS877098 in the GJB2 gene, and for the polymorphic deletions of GSTM1 and GSTT1 genes. We also investigated the frequency of variants in the mitochondrial genes MT-RNR1 and MT-TS1, which are known to harbor many hearing loss causative mutations. Our sample comprised 107 individuals with suggestive NIHL audiograms, 44 individuals with hearing impairment and non-suggestive NIHL audiograms, and 104 normal hearing individuals. A significant increase in the number of relatives affected by hearing impairment was detected in the NIHL group, when compared to the normal hearing group. Smoking habits, age and noise exposure time significantly affected the probability of NIHL. We did not detected any effect of the deafness-causing mutations 35delG and 167delT in the GJB2 gene, Δ (GJB6- D13S1830) and Δ (GJB6- D13S1854) in the GJB6 gene, and A1555G in the MT-RNR1 gene. There was no significant difference in allelic and genotypic frequencies of SNP RS87098 (gene GJB2), but the presence of the two genes encoding GSTM1 and GSTT1 enzymes was increased in the NIHL group. We did not detect any significant association of any of the 54 sequence variants in the mitochondrial genes MT-RNR1 and MT-TS1 (32 previously described and 22 novel) with the occurrence of NIHL. No significant associations were observed between NIHL and either the total number of sequence variants detected in each individual or haplotypes (combinations of two variants). The comparison of peroxides and sulfhydryl groups concentrations in serum from 15 individuals with NIHL and 15 individuals without NIHL did not show significant differences. In conclusion, our study demonstrated a significant effect of family history of hearing loss on the probability of presenting NIHL and pointed to a possible role of GSTT1 and GSTM1 enzymes on the susceptibility to this condition. These findings reinforce the idea that susceptibility to NIHL has a genetic basis.

ASSUNTO(S)

polimorfismos dos genes gjb2 gstm1 e gstt1 nihl mutações nos genes mitocondriais mt-rnr1 e mt-ts1 gjb2 gstm1 e gstt1 genes polimorphisms mt-rnr1 e mt-ts1 mutations mutações associadas à surdez deafness mutations genetic susceptibility pair susceptibilidade genética

ACESSO AO ARTIGO

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