Objectives: The primary goal of this study was to test the ability of 2f(1)
-f(2) distortion-product otoacoustic emissions (DPOAEs) to detect reduced c
ochlear function in the presence of normal behavioral sensitivity.
Design: A prospective study was performed in normal-hearing young adults us
ing simple and complex regression analyses to clarify the relationship betw
een ultrahigh frequency (UHF) hearing and DPOAE levels at lower frequencies
, as well as the influence of hearing levels for frequencies within the con
ventional test range and subject age on this association.
Methods: Average DPOAE levels between 4 to 8 kHz, which were elicited by eq
uilevel primary tones of low to moderate levels, were measured as level-fre
quency functions, or distortion-product (DP) grams, and related to the mean
UHF hearing levels from 11.2 to 20 kHz. The median hearing level for the U
HF hearing was used to separate subjects into good and poor UHF hearers. Th
is distinction was then used to compare DPOAE levels from 4 to 8 kHz for th
e 2 groups to determine if UHF hearing status influenced DPOAE levels at lo
wer frequencies.
Results: Simple regression analysis revealed that the 4- to 8-kHz DPOAE lev
els were significantly correlated with the pure-tone average (PTA) from 11.
2 to 20 kHz. However, the PTA for 4 and 8 kHz was also significantly correl
ated with the PTA for UHF hearing. Further multiple regression analyses rev
ealed that UHF hearing significantly and uniquely accounted for approximate
ly 14% of the variance in DPOAE levels from 4 to El kHz for most of the pri
mary-tone level combinations. In contrast, neither the PTA for the conventi
onal hearing range nor subject age contributed significantly to the DPOAE v
ariance.
Conclusions: The findings suggest that UHF hearing influences DPOAEs at sig
nificantly lower frequencies because emissions are sensitive to subtle chan
ges in outer hair cells not yet detected by pure-tone thresholds in this re
gion or because alterations in the basal cochlea affect the generation of l
ower-frequency DPOAEs originating from more apical cochlear regions.