The homozygote p.V27I/p.E114G variant of GJB2 is a putative indicator of nonsyndromic hearing loss in Chinese infants

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• 作者：Wen-xia Chen¹ ; Yue Huang¹ ; Xiao-lin Yang ; Bo Duan ; Ping Lu ; Yan Wang ; Zheng-min Xu ; ^{xuzhengmin@sh163.net" class="auth_mail" title="E-mail the corresponding author} ; ^{13916320945@163.com" class="auth_mail" title="E-mail the corresponding author}
• 关键词：GJB2 (connexin 26) ; Hereditary hearing loss ; p.V27I ; p.E114G
• 刊名：International Journal of Pediatric Otorhinolaryngology
• 出版年：2016
• 出版时间：May 2016
• 年：2016
• 卷：84
• 期：Complete
• 页码：48-51
• 全文大小：237 K

文摘

The gap junction β2 (GJB2) gene is associated with more than half of the recessive forms of hereditary hearing loss (HHL). However, the correlation between p.V27I and p.E114G variants of GJB2 and hearing phenotype remains controversial. This study aimed to clarify possible roles of these variants in Chinese infants with nonsyndromic hearing loss (NSHL). Hearing and gene tests were conducted in 300 infants (aged 0–3 months) with NSHL and 484 normal infants (aged 0–3 months). The p.V27I and p.E114G variants appeared frequently in both NSHL patients and normal controls. The allele and haplotype frequencies of p.V27I and p.E114G in patients and controls were compared, but no significant difference was observed (p = 0.44 and p = 0.26, respectively). Moreover, genotype frequencies of the p.V27I variant showed no significant difference between the two groups (p = 0.66). Interestingly, more homozygote p.V27I/p.E114G subjects were found in NSHL infants than in controls (5/484 and 13/300, respectively), most of whom (61.54%) had mild or moderate hearing losses. Our results indicate that homozygote p.V27I/p.E114G is associated with mild and moderate HHL.