Referenced in: none

Automatically associated channels: Kv7.1 , Kv7.4

Title: The contribution of genes involved in potassium-recycling in the inner ear to noise-induced hearing loss.

Authors: Lut Van Laer, Per-Inge Carlsson, Natacha Ottschytsch, Marie-Louise Bondeson, Annelies Konings, Ann Vandevelde, Nele Dieltjens, Erik Fransen, Dirk Snyders, Erik Borg, Adam Raes, Guy Van Camp

Journal, date & volume: Hum. Mutat., 2006 Aug , 27, 786-95

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/16823764

Abstract
Noise-induced hearing loss (NIHL) is one of the most important occupational diseases and, after presbyacusis, the most frequent cause of hearing loss. NIHL is a complex disease caused by an interaction between environmental and genetic factors. The various environmental factors involved in NIHL have been relatively extensively studied. On the other hand, little research has been performed on the genetic factors responsible for NIHL. To test whether the variation in genes involved in coupling of cells and potassium recycling in the inner ear might partly explain the variability in susceptibility to noise, we performed a case-control association study using 35 SNPs selected in 10 candidate genes on a total of 218 samples selected from a population of 1,261 Swedish male noise-exposed workers. We have obtained significant differences between susceptible and resistant individuals for the allele, genotype, and haplotype frequencies for three SNPs of the KCNE1 gene, and for the allele frequencies for one SNP of KCNQ1 and one SNP of KCNQ4. Patch-clamp experiments in high K+-concentrations using a Chinese hamster ovary (CHO) cell model were performed to investigate the possibility that the KCNE1-p.85N variant (NT_011512.10:g.21483550G>A; NP_00210.2:p.Asp85Asn) was causative for high noise susceptibility. The normalized current density generated by KCNQ1/KCNE1-p.85N channels, thus containing the susceptibility variant, differed significantly from that from wild-type channels. Furthermore, the midpoint potential of KCNQ1/KCNE1-p.85N channels (i.e., the voltage at which 50% of the channels are open) differed from that of wild-type channels. Further genetic and physiological studies will be necessary to confirm these findings.