[Amplitude modulation following response (AMFR)--a method for objective frequency specific audiologic diagnosis]. 1996

J Pethe, and K Begall, and R Mühler, and J K Lottmann
Abteilung für Experimentelle Audiologie und Medizinische Physik.

BACKGROUND The objective evaluation of the hearing threshold below 1kHz by means of early auditory potentials leads to problems caused by the discrepancy between the required steep rise edge of stimulus and the frequency specificity of the potentials. Therefore the aim of this study was to evaluate the potential role of the AMFR as a diagnostic tool for the assessment of hearing below 1 kHz. METHODS The threshold of the AMFR was compared to the behavioral threshold in 13 normal hearing subjects and 46 patients with hearing loss. The stimulus used was an amplitude-modulated tone at the carrier frequencies of 0.5 and 1 kHz, a modulation frequency of 40 Hz; the modulation depth was 80%. The introduction of an empiric detectibility criterion based on spectral analysis of the response curve allowed the investigator to minimize the examination time and objectify the interpretation of the response. Additional investigations by means of highpass-masking took place to estimate the frequency specificity of the AMFR. RESULTS The results show a good correspondence of the AMFR threshold to the behavioral threshold. Depending on hearing loss the mean values of differences between AMFR threshold and behavioral threshold are 3 dB - 13 dB. The degree of correspondence was highest in the patients with the most severe hearing loss. An influence of underlying cause of the hearing loss could not be found. Additionally the frequency specificity of the response potential was proven with high-pass masking in normal hearing subjects. Masking with cut-off frequencies above the carrier frequencies had no influence on the response while masking at the carrier frequency resulted in a strong reduction of the response curve. CONCLUSIONS The results show that the 40 Hz-AMFR is a suitable method for the objective frequency-specific assessment of hearing in adults. Problems in the clinical use of the AMFR are caused by the long investigation time and the dependence of the potentials on the state of wakeness.

UI MeSH Term Description Entries
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009464 Neuroma, Acoustic A benign SCHWANNOMA of the eighth cranial nerve (VESTIBULOCOCHLEAR NERVE), mostly arising from the vestibular branch (VESTIBULAR NERVE) during the fifth or sixth decade of life. Clinical manifestations include HEARING LOSS; HEADACHE; VERTIGO; TINNITUS; and FACIAL PAIN. Bilateral acoustic neuromas are associated with NEUROFIBROMATOSIS 2. (From Adams et al., Principles of Neurology, 6th ed, p673) Acoustic Neuroma,Melanocytic Vestibular Schwannoma,Schwannoma, Acoustic,Schwannoma, Vestibular,Acoustic Neuroma, Cerebellopontine Angle,Acoustic Tumor,Angle Tumor,Cerebellopontine Angle Acoustic Neuroma,Cerebellopontine Angle Tumor,Neurilemmoma, Acoustic,Neurilemoma, Acoustic,Neurinoma of the Acoustic Nerve,Neurinoma, Acoustic,Neuroma, Acoustic, Unilateral,Vestibular Schwannoma,Acoustic Neurilemmoma,Acoustic Neurilemmomas,Acoustic Neurilemoma,Acoustic Neurilemomas,Acoustic Neurinoma,Acoustic Neurinomas,Acoustic Neuromas,Acoustic Schwannoma,Acoustic Schwannomas,Acoustic Tumors,Angle Tumor, Cerebellopontine,Angle Tumors,Angle Tumors, Cerebellopontine,Cerebellopontine Angle Tumors,Melanocytic Vestibular Schwannomas,Neurilemmomas, Acoustic,Neurilemomas, Acoustic,Neurinomas, Acoustic,Neuromas, Acoustic,Schwannoma, Melanocytic Vestibular,Schwannomas, Acoustic,Schwannomas, Melanocytic Vestibular,Schwannomas, Vestibular,Tumor, Acoustic,Tumor, Angle,Tumor, Cerebellopontine Angle,Tumors, Acoustic,Tumors, Angle,Tumors, Cerebellopontine Angle,Vestibular Schwannoma, Melanocytic,Vestibular Schwannomas,Vestibular Schwannomas, Melanocytic
D010897 Pitch Discrimination The ability to differentiate sound frequency or pitch. Discrimination, Pitch,Pitch Discriminations
D005260 Female Females
D006313 Hearing Loss, Central Hearing loss due to disease of the AUDITORY PATHWAYS (in the CENTRAL NERVOUS SYSTEM) which originate in the COCHLEAR NUCLEI of the PONS and then ascend bilaterally to the MIDBRAIN, the THALAMUS, and then the AUDITORY CORTEX in the TEMPORAL LOBE. Bilateral lesions of the auditory pathways are usually required to cause central hearing loss. Cortical deafness refers to loss of hearing due to bilateral auditory cortex lesions. Unilateral BRAIN STEM lesions involving the cochlear nuclei may result in unilateral hearing loss. Central Hearing Loss,Cortical Deafness,Deafness, Cortical
D006314 Hearing Loss, Conductive Hearing loss due to interference with the mechanical reception or amplification of sound to the COCHLEA. The interference is in the outer or middle ear involving the EAR CANAL; TYMPANIC MEMBRANE; or EAR OSSICLES. Conductive Hearing Loss
D006319 Hearing Loss, Sensorineural Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM. Deafness Neurosensory,Deafness, Neurosensory,Deafness, Sensoryneural,Neurosensory Deafness,Sensorineural Hearing Loss,Sensoryneural Deafness,Cochlear Hearing Loss,Hearing Loss, Cochlear,Deafnesses, Neurosensory,Deafnesses, Sensoryneural,Neurosensory Deafnesses,Sensoryneural Deafness,Sensoryneural Deafnesses
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths

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