PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Auditory Threshold”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,387 records · Page 77Linked to original sources

Thresholds for short-latency auditory-evoked potentials to tones in notched noise in normal-hearing and hearing-impaired subjects.

The thresholds for the short-latency auditory evoked potentials (SLAEPs) to short-duration tones presented in notched-noise masking were evaluated in 20 normal-hearing and 20 hearing-impaired subjects. The differences (dB) between these thresholds (dB nHL) and the pure-tone behavioral thresholds (dB HL) across all 40 subjects were 11.6, 6.1, 6.3 and 0.8 dB for 500, 1,000, 2,000 and 4,000 Hz, respectively. These differences were significantly smaller for the hearing-impaired subjects than for the normal-hearing subjects. Ninety-eight percent of the SLAEP threshold estimations were within 30 dB of the subjects' pure-tone behavioral thresholds and 91% were within 20 dB.

Adolescent↗

Acoustic reflex crossover artifacts in infants and young children.

Crossover artifacts occur when the probe microphone of an impedance instrument directly responds to vibratory-acoustic energy that crosses the skull from the stimulus transducer on the contralateral ear. The resulting meter deflections are subjectively similar to and may be interpreted as actual acoustic reflexes (ARs) by unsuspecting examiners. In this study, infants and young children aged 10 days to 6 years 9 months were fit with earplugs to eliminate the AR and were examined for artifact incidence and threshold. Results indicate a high rate of occurrence of the crossover artifact in the youngest subjects, when probe tones of 220 and 660 Hz were used with stimuli of 500 and 1,000 Hz. Artifact thresholds were found as low as at a 92-dB hearing level, and an inverse relationship was shown between age and artifact incidence and threshold.

Acoustic Impedance Tests↗

Topography of spiral ganglion projections to cochlear nucleus during postnatal development in cats.

A fundamenntal organizational principle of the central auditory system is that virtually all areas are tonotopically organized. However, we know very little about the timing or mechanisms that are responsible for the development of this organization. When cats are born, their auditory nervous systems are extremely immature, and their hearing thresholds are very high. Until postnatal days 7-10 (P7-10), cats have behavioral and physiological thresholds which are near or above the pain threshold for adults and also have poor frequency selectivity. Physiological thresholds for auditory nerve fibers and cochlear nucleus neurons are typically above 100-120 dB SPL (sound pressure level re 20 microPa). Three weeks later (at approximately P31), the sensitivity and frequency discrimination (tuning) of these neurons approximate adult values. This study examines the development of the tonotopic projections from the spiral ganglion to the cochlear nucleus during the period in cat development in which the auditory system undergoes the transition from being essentially nonfunctional to having adult-like function. With the animals heavily anesthetized, the cochleas were surgically exposed in kittens ranging in age from P6 to P45. Focal injections of Neurobiotin (NB) were made into Rosenthal's canal, labeling a small cluster of cells in the spiral ganglion of each cochlea. The projections of these labeled cells were visualized as frequency-specific bands of labeled axons and terminals in all major subdivisions of the cochlear nucleus. The thickness of these bands (i.e., the dimension of the bands orthogonal to the isofrequency representation and across the frequency gradient) were measured and compared to similar projections in adults. As in adult cats, the thickness of the bands varied only slightly with the location of the injection site (frequency representation) over a range of 1-7 mm from the cochlear base (45-13 kHz). Moreover, band thickness did not vary significantly with age. These data indicate that the tonotopic organization of spiral ganglion projections to the cochlear nucleus is as precise in kittens as young as P6 as it is in adults.

Afferent Pathways↗

Growth of loudness in listeners with cochlear hearing losses: recruitment reconsidered.

This article examines how loudness grows with increasing intensity near threshold in five listeners with hearing losses of predominantly cochlear origin. It provides evidence against the pervasive and long-held notion that such listeners show abnormally rapid loudness growth near their elevated thresholds. As in a previous study for listeners with normal hearing, loudness functions near threshold were derived from loudness matches between a pure tone and four- or ten-tone complexes using a simple model of loudness summation. This study assumed that the loudness function had the same form for any component of a complex, but a scale factor that depended on the amount of hearing loss allowed the loudness at threshold to vary with frequency. The best-fitting loudness functions had low-level local exponents [i.e., slopes of the low-level loudness function plotted as log(loudness) versus log(intensity)] that were within the normal range. At 0 dB SL, the average local exponents were 1.26 for the listeners with hearing losses compared with 1.31 for normal listeners, which indicates that loudness near threshold grows at similar rates in normal listeners and listeners with hearing losses. The model also indicated that, on average, the loudness at threshold doubled for every 16 dB of hearing loss. The increased loudness at threshold, together with somewhat enlarged local exponents around 20 dB SL, accounts for the near-normal loudness often obtained for high-SPL tones in listeners with hearing losses. Such loudness functions are consistent with the steep functions shown by classical data on loudness matches between tones for which thresholds are normal and tones for which thresholds are elevated. Thus, the present data indicate that an abnormally large loudness at an elevated threshold is likely to be a better definition of recruitment than the classical definition of it as an abnormally rapid growth of loudness above an elevated threshold.

Adult↗

Encoding of alternating acoustical signals in the medial geniculate body of guinea pigs.

In unanaesthetized guinea pigs 102 single units of the medial geniculate body were recorded under acoustical stimulation with alternating noise and tone impulses. The temporal parameters of the signals were chosen in close relation to psychoacoustical pulsation-threshold measurements. Most units showed a strong interaction between the responses of the non-simultaneously presented signal components (temporal suppression). The phasic part of each impulse-evoked response was more affected by the suppression than the tonic part. Thus, two regions of responsiveness could be verified: a region of pure tonic discharge and a region of tonic and phasic discharge. The borderline between both regions was defined as 'on-threshold'. The temporal suppression effect of the discharge rate did depend on impulse duration, impulse shape, gap duration, and the levels of the signal components. The overall unit-response characteristic-especially the lac of temporal onset information--suggested a close relation between psychoacoustical pulsation threshold and physiological 'on-threshold'.

Acoustic Stimulation↗

Deterioration of hearing function in mice with neural crest defect.

Cochlear potentials were recorded in black-eyed white-mutant mice (strains W/Wv and S1/S1d) during the first months of postnatal life. In these animals melanocytes from the neural crest do not reach the stria vascularis. Hearing thresholds indicated by the compound action potential of the auditory nerve progressively increased. Hearing loss in comparison with the control CBA mice amounted 40 dB six weeks after birth, at eight months practically all mutants were deaf. Endocochlear potential was near zero already in the majority of 6 week-old animals. Abnormalities were observed also in intracellular potentials of the stria vascularis cells which were recorded in vitro and dye-marked. While in marginal cells of CBA mice positive potentials of about 10 mV were recorded, potentials of marginal cells in mutants were near zero. Basal cell potentials were negative in CBA mice (approximately -25 mV) and positive in young mutants (approximately +12 mV). However, in mutants older than 3 months the intracellular potentials of basal cells changed to negativity (approximately -10 mV). The results demonstrate gradual deterioration of hearing function observed in both W/Wv and S1/S1d mutants during first months of the postnatal life. In addition to the dysfunction of stria vascularis, where intermediate cells are missing, also the function of receptors progressively deteriorates.

Action Potentials↗

Effects of high-frequency cue reduction on the comprehension of distorted speech.

Forty-five subjects with sharply sloping sensorineural high-frequency hearing losses were examined for comprehension with a tape containing sentences that had been time-compressed (250 words/min), interrupted, (50 msec on-50 msec off), and masked with speech-spectrum noise (+2 dB S/N) in that order. All subjects yielded normal speech reception thresholds, and generally normal scores on the Northwestern University Auditory Test No. 6. Distorted-speech testing was completed at 40 dB SL. Subjects with losses at 2 kHz and above were able to comprehend only 50, 65, and 68% of compressed, interrupted, and noise-masked sentences, respectively. In contrast, subjects with losses at 3 kHz and above performed poorer than normal controls by 11.3, 12.5, and 8% points respectively, while subjects within normal hearing sensitivity at 3 kHz performed as well as controls (maximum drop of 4.6 points with noise-masking). The multiplicative hypothesis was upheld in that the performance of subjects with severe high-frequency deficiencies was much poorer than one would predict on the basis of what is known about performance on these tests with either filtering alone or other distortions alone. These subjects, most especially those with severe frequency deficiencies, outperformed by up to 29 percentage points the mean scores of groups of normals given the same test items and distortion conditions, but listening through filtering that simulated the hearing loss of subjects in this study. It was suggested that hypacusics with high-frequency hearing losses can learn to use residual cues efficiently and that it is not altogether permissible to model sensorineural high-frequency losses with normal-hearing subjects using frequency filtering.

Adult↗

High-frequency hearing thresholds in young adults using a commercially available audiometer.

Test and re-test high-frequency (10-20 kHz) thresholds were obtained for 200 ears of 100 normally hearing (0.25-8 kHz) young adults (18-28 years old) using a Beltone 2000 audiometer and Sennheiser HD 250 earphones referenced to sound pressure levels developed in a Bruel and Kjaer flat-plate coupler. Normative high-frequency thresholds could not be recommended for clinical use due to the very large intersubject threshold variability. This occurred even though test versus re-test thresholds were not significantly different (p greater than 0.05) at any frequency. However, comparisons of the test minus re-test threshold for individual ears were within a clinically acceptable range of +/- 10 dB for at least 95% of the ears at each frequency. Future research should concern intrasubject threshold reliability and variability rather than specifying intersubject normative thresholds.

Adolescent↗

Comparison of continuous and pulsed stimuli in contralateral acoustic reflex threshold measurements.

Continuous pure-tone stimuli are traditionally used for contralateral acoustic reflex threshold (ART) testing. The GSI-33 middle ear analyzer provides an option of pulsed stimuli for contralateral ART testing. This study compared ARTs for the steady and the pulsed stimuli for 100 ears. Lower ARTs were consistently obtained with the continuous rather than the pulsed stimulus for more than 90% of the thresholds.

Acoustic Stimulation↗

A further examination of the use of the stapedius reflex in the diagnosis of acoustic neuroma.

Criteria proposed by ANDERSON et al. for the diagnosis of early acoustic neuromas using the acoustic stapedius reflex were examined. Populations of normal hearers and subjects with sensorineural hearing losses were studied and yielded high false-positive detection rates by the threshold criteria. It is suggested that the threshold asymmetry of the reflex may be more useful than the absolute threshold.

Acoustic Stimulation↗

Mechanisms of increased sensitivity to noise and light in migraine headache.

To determine whether phonophobia is a manifestation of loudness recruitment, the hearing and auditory discomfort thresholds to an 8000 Hz tone were measured during the headache-free interval and again during an attack of migraine in 16 migraine sufferers. The visual discomfort threshold was also determined. For comparison, measures were taken in 16 non-headache controls of similar age and sex distribution. Auditory and visual discomfort thresholds decreased substantially during attacks of migraine. Increases (three subjects) or decreases (three subjects) in hearing threshold during attacks of migraine were significantly greater than the variation recorded in control subjects from Session 1 to Session 2. The findings do not support the view that phonophobia in migraine is a manifestation of loudness recruitment, although cochlear disturbances might mediate hearing loss in some cases. Disruption of central sensory processing mechanisms during migraine could increase sensitivity to quiet sounds, and contribute to phono- and photophobia.

Adult↗

Topographic representation of auditory space in the superior colliculus of adult ferrets after monaural deafening in infancy.

1. We have investigated the role of monaural cues provided by the outer ear in the construction of a map of auditory space in the superior colliculus. Single-unit recordings were made from the superior colliculus of adult ferrets that were deprived of binaural inputs by surgically ablating the ipsilateral cochlea on postnatal day 21 or 24. 2. The spatial response properties of auditory units in the deeper layers of this nucleus were studied using white-noise bursts presented under free-field conditions in an anechoic chamber. The thresholds of the units recorded in the monaural ferrets were not significantly different from those recorded in the superior colliculus of normal adult ferrets. In both groups the unit thresholds varied by 30-50 dB in each region of the superior colliculus. 3. In normal and monaural ferrets the elevation tuning tended to be sharper than the azimuth tuning. At sound levels of approximately 10 dB above threshold the auditory units recorded in both groups of animals were tuned to a specific region of space that was restricted in azimuth and elevation. The spatial location at which the maximum response was obtained (auditory best position) varied topographically in azimuth along the rostrocaudal axis of the nucleus and in elevation along the mediolateral axis. 4. The azimuthal distribution of best positions associated with each recording location in the superior colliculus of the monaural ferrets and the alignment between this dimension of the auditory map and that of the visual map in the overlying superficial layers were no different from those found at corresponding near-threshold sound levels in normal ferrets. 5. Elevation spatial selectivity was examined in a smaller sample of units. Although elevation best positions shifted downward from the medial to the lateral side of the nucleus in both normal and monaural ferrets, we found that the topography of the auditory representation and its alignment with the visual representation were statistically different in the two groups of animals. 6. Increasing the sound level does not affect the representation of auditory space in normal ferrets. However, when the stimulus level presented to monoaural ferrets was increased, the receptive fields either expanded so that the responses were no longer tuned to any particular region of space, or the responses remained tuned but exhibited a marked shift in the value of the best position.(ABSTRACT TRUNCATED AT 400 WORDS)

Acoustic Stimulation↗

Recoveries of whole-nerve AP thresholds, amplitudes and tuning curves in gerbils following noise exposure.

The recoveries of whole-nerve action potential (AP) thresholds, AP amplitudes and AP tuning curves in gerbils were monitored following two weeks of exposure to band-pass noise at 85 dBA. Recordings were made by means of electrodes chronically implanted in the subjects' bullas. The noise exposure caused threshold elevations in all of our subjects, with the greatest shifts occurring an octave or more above the 2 kHz upper cutoff frequency of the noise. The magnitudes of the shifts varied greatly (up to 26 dB) across subjects. Thresholds of animals with the smallest initial loss of sensitivity returned to pre-exposure values within 16 days, while those of animals with greater initial losses remained elevated beyond 16 days. AP amplitudes and AP tuning curves (APTCs) were most affected at frequencies where the initial threshold shifts were greatest. At these frequencies AP amplitudes were reduced, and APTCs showed broadened tips, reduced tip-to-tail ratios, and in some cases a shift in the frequency of the tip. These effects did not necessarily reverse with threshold recovery, suggesting that AP amplitudes and AP tuning curves are more sensitive indices of acoustic injury than are AP thresholds.

Action Potentials↗

Cubic distortion product otoacoustic emissions in young and aged chinchillas exposed to low-frequency noise.

The aim of this study was to examine susceptibility to noise-induced hearing loss in animals with and without age-related hearing loss (AHL), using cubic distortion product otoacoustic emissions (CDPs) to assess the functional status of the outer hair cell (OHC) system. Subjects were young (< or = 3-yr-old) and aged (10- to 15-yr-old) chinchillas. CDP thresholds and input/output (I/O) functions were measured before and after exposure to 95 dB or 106 dB SPL low-frequency noise. The results indicate that (a) aging in the chinchilla is associated with significant elevations of CDP thresholds and depression of CDP I/O functions, (b) noise exposures cause equivalent CDP threshold elevations and amplitude reductions in young animals with normal hearing and older animals with AHL, and (c) CDP threshold and amplitude measures provide information that complements evoked potentials measured from the auditory midbrain.

Aging↗

Age-dependent changes in susceptibility to ototoxic hearing loss.

Several species undergo age-dependent changes in susceptibility to noise-induced and drug-induced hearing loss. In this experiment 18-day-old mice were given 200 mg/kg kanamycin plus varying doses of bumetanide (20, 30 or 40 mg/kg). Thresholds of the scalp-recorded compound action potential of the auditory nerve indicated that diuretic doses of 30 and 40 mg/kg produced significant loss of hearing sensitivity. Thirty-eight-day-old mice were then treated with 200 mg/kg kanamycin plus 40 mg/kg bumetanide and demonstrated no loss of hearing sensitivity. These results confirm the existence of age-dependent changes in susceptibility to ototoxic hearing loss in mice. Furthermore, the treatment, consisting of two injections on the same day, offers promise as a means of defining the critical period of susceptibility in greater detail than has been possible with aminoglycosides alone.

Aging↗