Dataset Information

Distortion-product otoacoustic emission suppression tuning curves in hearing-impaired humans.

ABSTRACT: Distortion-product otoacoustic emission (DPOAE) suppression tuning curves (STCs) were measured in 65 hearing-impaired (HI) subjects at f(2) frequencies of 2.0, 2.8, 4.0, and 5.6 kHz and L(2) levels relative to sensation level (SL) from 10 dB to as much as 50 dB. Best frequency, cochlear-amplifier gain (tip-to-tail difference, T-T), and tuning (Q(ERB)) were estimated from STCs. As with normal-hearing (NH) subjects, T-T differences and Q(ERB) decreased as L(2) increased. T-T differences and Q(ERB) were reduced in HI ears (compared to normal) for conditions in which L(2) was fixed relative to behavioral threshold (dB SL). When STCs were compared with L(2) at constant sound pressure levels (dB SPL), differences between NH and HI subjects were reduced. The large effect of level and small effect of hearing loss were both confirmed by statistical analyses. Therefore, the magnitude of the differences in DPOAE STCs between NH and HI subjects is mainly dependent on the manner in which level (L(2)) is specified. Although this conclusion may appear to be at odds with previous, invasive measures of cochlear-response gain and tuning, the apparent inconsistency may be resolved when the manner of specifying stimulus level is taken into account.

SUBMITTER: Gruhlke A

PROVIDER: S-EPMC3505205 | biostudies-other | 2012 Nov

REPOSITORIES: biostudies-other

ACCESS DATA

Similar Datasets

Project description:BackgroundAlthough several candidate-gene association studies have been conducted to investigate noise-induced hearing loss (NIHL) in humans, most are underpowered, unreplicated, and account for only a fraction of the genetic risk. Mouse genome-wide association studies (GWASs) have revolutionized the field of genetics and have led to the discovery of hundreds of genes involved in complex traits. The hybrid mouse diversity panel (HMDP) is a collection of classic inbred and recombinant inbred strains whose genomes have been either genotyped at high resolution or sequenced. To further investigate the genetics of NIHL, we report the first GWAS based on distortion product otoacoustic emission (DPOAE) measurements and the HMDP.MethodsA total of 102 strains (n = 635) from the HMDP were evaluated based on DPOAE suprathreshold amplitudes before and after noise exposure. DPOAE amplitude variation was set at 60 and 70 dB SPL of the primary tones for each frequency separately (8, 11.3, 16, 22.6, and 32 kHz). These values provided an indirect assessment of outer hair cell integrity. Six-week-old mice were exposed for 2 h to 10 kHz octave-band noise at 108 dB SPL. To perform local expression quantitative trait locus (eQTL) analysis, gene expression microarray profiles were generated using cochlear RNA from 64 hybrid mouse strains (n = 3 arrays per strain).ResultsSeveral new loci were identified and positional candidate-genes associated with NIHL were prioritized, especially after noise exposure (1 locus at baseline and 5 loci after exposure). A total of 35 candidate genes in these 6 loci were identified with at least 1 probe whose expression was regulated by a significant cis-eQTL in the cochlea. After careful analysis of the candidate genes based on cochlear gene expression, 2 candidate genes were prioritized: Eya1 (baseline) and Efr3a (post-exposure).Discussion and conclusionFor the first time, an association analysis with correction for population structure was used to map several loci for hearing traits in inbred strains of mice based on DPOAE suprathreshold amplitudes before and after noise exposure. Our results identified a number of novel loci and candidate genes for susceptibility to NIHL, especially the Eya1 and Efr3a genes. Our findings validate the power of the HMDP for detecting NIHL susceptibility genes.

Dataset Information

Distortion-product otoacoustic emission suppression tuning curves in hearing-impaired humans.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets