Auditory neuropathy spectrum disorder (ANSD): a distortion product otoacoustic emissions (DPOAEs) study

Abstract

Abstract Background Auditory neuropathy spectrum disorder (ANSD) is characterized by normal OHCs function as shown by intact cochlear microphonics (CMs) and/or otoacoustic emissions (OAEs); absent or grossly abnormal auditory brainstem responses (ABRs) and absent middle ear muscle reflexes. This study is designed to address whether the input/output function of distortion product OAEs (DPOAEs I/O) in ANSD patients is similar or different from normal hearing subjects. This work included 2 groups: control group (GI) composed of 20 normal hearing subjects and study group (GII) consisted of 20 patients with ANSD. All cases were subjected to basic audiological evaluation, DPOAEs I/O function recorded at four frequencies of 2f1-f2 and 5 intensity levels of L1 and L2. Results DPOAEs amplitudes were significantly higher in ANSD group when compared with control. The pattern of DPOAEs I/O function was different in ANSD and it was dependent on the frequency and intensity of the stimulus. Conclusions Despite normal DPOAEs recordings in ANSD patients, their amplitudes and DP I/O function are different from that of normal hearing subjects. This finding suggested different OHC pattern of activity in ANSD patients.