Background The authors reviewed the evidence regarding the existence of age-related declines in central auditory processes and the consequences of any such declines for everyday communication. Purpose This report summarizes the review process and presents its findings. Data Collection and Analysis The authors reviewed 165 articles germane to central presbycusis. Of the 165 articles, 132 articles with a focus on human behavioral measures for either speech or nonspeech stimuli were selected for further analysis. Results For 76 smaller-scale studies of speech understanding in older adults reviewed, the following findings emerged: (1) the three most commonly studied behavioral measures were speech in competition, temporally distorted speech, and binaural speech perception (especially dichotic listening); (2) for speech in competition and temporally degraded speech, hearing loss proved to have a significant negative effect on performance in most of the laboratory studies; (3) significant negative effects of age, unconfounded by hearing loss, were observed in most of the studies of speech in competing speech, time-compressed speech, and binaural speech perception; and (4) the influence of cognitive processing on speech understanding has been examined much less frequently, but when included, significant positive associations with speech understanding were observed. For 36 smaller-scale studies of the perception of nonspeech stimuli by older adults reviewed, the following findings emerged: (1) the three most frequently studied behavioral measures were gap detection, temporal discrimination, and temporal-order discrimination or identification; (2) hearing loss was seldom a significant factor; and (3) negative effects of age were almost always observed. For 18 studies reviewed that made use of test batteries and medium-to-large sample sizes, the following findings emerged: (1) all studies included speech-based measures of auditory processing; (2) 4 of the 18 studies included nonspeech stimuli; (3) for the speech-based measures, monaural speech in a competing-speech background, dichotic speech, and monaural time-compressed speech were investigated most frequently; (4) the most frequently used tests were the Synthetic Sentence Identification (SSI) test with Ipsilateral Competing Message (ICM), the Dichotic Sentence Identification (DSI) test, and time-compressed speech; (5) many of these studies using speech-based measures reported significant effects of age, but most of these studies were confounded by declines in hearing, cognition, or both; (6) for nonspeech auditory-processing measures, the focus was on measures of temporal processing in all four studies; (7) effects of cognition on nonspeech measures of auditory processing have been studied less frequently, with mixed results, whereas the effects of hearing loss on performance were minimal due to judicious selection of stimuli; and (8) there is a paucity of observational studies using test batteries and longitudinal designs. Conclusions Based on this review of ...

This study compared monosyllabic word recognition in quiet, noise, and noise with reverberation for 15 monolingual American English speakers and 12 Spanish-English bilinguals who had learned English prior to 6 years of age and spoke English without a noticeable foreign accent. Significantly poorer word recognition scores were obtained for the bilingual listeners than for the monolingual listeners under conditions of noise and noise with reverberation, but not in quiet. Although bilinguals with little or no foreign accent in their second language are often assumed by their peers, or their clinicians in the case of hearing loss, to be identical in perceptual abilities to monolinguals, the present data suggest that they may have greater difficulty in recognizing words in noisy or reverberant listening environments.

Temporal discrimination was measured using a gap discrimination paradigm for three groups of listeners with normal hearing: (1) ages 18-30, (2) ages 40-52, and (3) ages 62-74 years. Normal hearing was defined as pure-tone thresholds < or = 25 dB HL from 250 to 6000 Hz and < or = 30 dB HL at 8000 Hz. Silent gaps were placed between 1/4-octave bands of noise centered at one of six frequencies. The noise band markers were paired so that the center frequency of the leading marker was fixed at 2000 Hz, and the center frequency of the trailing marker varied randomly across experimental runs. Gap duration discrimination was significantly poorer for older listeners than for young and middle-aged listeners, and the performance of the young and middle-aged listeners did not differ significantly. Age group differences were more apparent for the more frequency-disparate stimuli (2000-Hz leading marker followed by a 500-Hz trailing marker) than for the fixed-frequency stimuli (2000-Hz lead and 2000-Hz trail). The gap duration difference limens of the older listeners increased more rapidly with frequency disparity than those of the other listeners. Because age effects were more apparent for the more frequency-disparate conditions, and gap discrimination was not affected by differences in hearing sensitivity among listeners, it is suggested that gap discrimination depends upon temporal mechanisms that deteriorate with age and stimulus complexity but are unaffected by hearing loss.

Objective The objective of this study was to describe the auditory evoked response to silent gaps for a group of older adults using stimulus conditions identical to those used in psychophysical studies of gap detection. Design The P1-N1-P2 response to the onsets of stimuli (markers) defining a silent gap for within-channel (spectrally identical markers) and across-channel (spectrally different markers) conditions was examined using four perceptually-equated gap durations. Study Sample A group of 24 older adults (mean age = 63 years) with normal hearing or minimal hearing loss participated. Results Older adults exhibited neural activation patterns that were qualitatively different and more frontally oriented than those observed in a previous study (Lister et al., 2007) of younger listeners. Older adults showed longer P2 latencies and larger P1 amplitudes than younger adults, suggesting relatively slower neural travel time and altered auditory inhibition/arousal by irrelevant stimuli. Conclusion Older adults appeared to recruit later-occurring T-complex-like generators for gap processing, compared to earlier-occurring T-complex-like generators by the younger group. Early and continued processing of channel cues with later processing of gap cues may represent the inefficiency of the aging auditory system and may contribute to poor speech understanding in noisy, real-world listening environments.

Objectives-The objective of this study was to describe the cortical evoked response to silent gaps in a group of young adults with normal hearing using stimulus conditions identical to those used in psychophysical studies of gap detection. Specifically, we sought to examine the P1-N1-P2 auditory evoked response to the onsets of stimuli (markers) defining a silent gap for withinchannel (spectrally identical markers) and across-channel (spectrally different markers) conditions using four perceptually-equated gap durations. It was hypothesized that (1) P1, N1, and P2 would be present and consistent for 1st marker (before the gap) onsets; (2) for within-channel markers, P1, N1, and P2 would be present for 2nd marker (after the gap) onsets only when the gap was of a duration equal to or larger than the behaviorally measured gap detection threshold; and (3) for the across-channel conditions, P1, N1, and P2 would be present for 2nd marker onsets regardless of gap duration. This is expected due to the additional cue of frequency change following the gap.Design-Twelve young adults (mean age 26 years) with normal hearing participated. Withinchannel and across-channel gap detection thresholds were determined using an adaptive psychophysical procedure. Next, cortical auditory evoked potentials (P1-N1-P2) were recorded with a 32-channel Neuro-scan™ electroencephalogram system using within-channel and acrosschannel markers identical to those used for the psychophysical task and four perceptually weighted gap durations: (1) individual listener's gap detection threshold; (2) above gap detection threshold; (3) below gap detection threshold; and (4) a 1-ms gap identical to the gap in the standard interval of the psychophysical task. P1-N1-P2 peak latencies and amplitudes were analyzed using repeated-measures analyses of variance. A temporal-spatial principal component analysis was also conducted.Results-The latency of P2 and the amplitude of P1, N1, and P2 were significantly affected by the acoustic characteristics of the 2nd marker as well as the duration of the gap. Larger amplitudes and shorter latencies were generally found for the conditions in which the acoustic cues were most salient (e.g., across-channel markers, 1st markers, large gap durations). Interestingly, the temporal-spatial principal component analysis revealed activity elicited by gap durations equal to gap detection threshold in the latency regions of 167 and 183 ms for temporal-parietal and rightfrontal spatial locations.Address for correspondence: Jennifer Lister, Department of Communication Sciences and Disorders, University of South Florida, 4202 E. Fowler Ave. PCD 1017, Tampa, FL 33620. jlister@cas.usf.edu.. HHS Public Access Author Manuscript Author ManuscriptAuthor Manuscript Author ManuscriptConclusions-The cortical response to a silent gap is unique to specific marker characteristics and gap durations among young adults with normal hearing. Specifically, when the onset of the 2nd marker is perceptually salient, the amplitude of the P1-N1-P2 re...

Ovcs thc lasl century, research in the area of age-related hearing loss has provided a vast mount of knowledge rcgarding agc-related errtlcts on the amatoiny and physiology of the auditory system. As we enter the new millennium, rcscarchers arc bcginning to shirt their attention towards developing nicthods of moduleling the efkcts of ape-related hearing loss arid the development of efficacious intervcnrion slralcgies to meel all of a n individuiil's hearinprelated rehabilitative needs. The purpose of this rcvicw is lo provide a friimework for considering houz the biological aspects of the aging auditory systcm intcract with the nmst co~nnion current therapeutic intervention for age-related hearing loss-the usc of amplification---tind also hou. the biological aspects point to other potential intensention strategies.

Objective: Cortical auditory evoked potentials, including mismatch negativity (MMN) and P3a to pure tones, harmonic complexes, and speech syllables, were examined across groups of trained musicians and nonmusicians. Because of the extensive formal and informal auditory training received by musicians throughout their lifespan, it was predicted that these electrophysiological indicators of preattentive pitch discrimination and involuntary attention change would distinguish musicians from nonmusicians and provide insight regarding the influence of auditory training and experience on central auditory function.Design: A total of 102 (67 trained musicians, 35 nonmusicians) righthanded young women with normal hearing participated in three auditory stimulus conditions: pure tones (25 musicians/15 nonmusicians), harmonic tones (42 musicians/20 nonmusicians), and speech syllables (26 musicians/15 nonmusicians). Pure tone and harmonic tone stimuli were presented in multideviant oddball paradigms designed to elicit MMN and P3a. Each paradigm included one standard and two infrequently occurring deviants. For the pure tone condition, the standard pure tone was 1000 Hz, and the two deviant tones differed in frequency from the standard by either 1.5% (1015 Hz) or 6% (1060 Hz). The harmonic tone complexes were digitally created and contained a fundamental frequency (F0) and three harmonics. The amplitude of each harmonic was divided by its harmonic number to create a natural amplitude contour in the frequency spectrum. The standard tone was G4 (F0 ϭ 392 Hz), and the two deviant tones differed in fundamental frequency from the standard by 1.5% (F0 ϭ 386 Hz) or 6% (F0 ϭ 370 Hz). The fundamental frequencies of the harmonic tones occur within the average female vocal range. The third condition to elicit MMN and P3a was designed for the presentation of speech syllables (/ba/ and /da/) and was structured as a traditional oddball paradigm (one standard/one infrequent deviant). Each speech stimulus was presented as a standard and a deviant in separate blocks. P1-N1-P2 was elicited before each oddball task by presenting each auditory stimulus alone in single blocks. All cortical auditory evoked potentials were recorded in a passive listening condition.Results: Incidental findings revealed that musicians had longer P1 latencies for pure tones and smaller P1 amplitudes for harmonic tones than nonmusicians. There were no P1 group differences for speech stimuli. Musicians compared with nonmusicians had shorter MMN latencies for all deviances (harmonic tones, pure tones, and speech). Musicians had shorter P3a latencies to harmonic tones and speech but not to pure tones. MMN and P3a amplitude were modulated by deviant frequency but not by group membership. Conclusions:Formally trained musicians compared with nonmusicians showed more efficient neural detection of pure tones and harmonic tones; demonstrated superior auditory sensory-memory traces for acoustic features of pure tones, harmonic tones, and speech; and revealed enhanced sensitivity to...

Deficits in temporal resolution and/or the precedence effect may underlie part of the speech understanding difficulties experienced by older listeners in degraded acoustic environments. In a previous investigation, R. Roberts and J. Lister (2004) identified a positive correlation between measures of temporal resolution and the precedence effect, specifically across-channel gap detection (as measured dichotically) and fusion. Across-channel gap detection may also be measured using frequency-disparate markers. Thus, the present investigation was designed to determine if the relation is specific to dichotic gap detection or may generalize to all types of across-channel gap detection. Gap-detection thresholds (GDTs) for fixed-frequency and frequency-disparate markers and lag-burst thresholds (LBTs) were measured for 3 groups of listeners: young with normal hearing sensitivity (YNH), older with normal hearing sensitivity (ONH), and older with sensorineural hearing loss (OIH). Also included were conditions of diotic and dichotic GDT. Largest GDTs were measured for the frequency-disparate markers, whereas largest LBTs were measured for the fixed-frequency markers. ONH and OIH listeners exhibited larger frequency-disparate and dichotic GDTs than YNH listeners. Listener age and hearing loss appeared to influence temporal resolution for frequency-disparate and dichotic stimuli, which is potentially important for the resolution of timing cues in speech. Age and hearing loss did not significantly influence fusion as measured by LBTs. Within each participant group, most GDTs and LBTs were positively, but not significantly, correlated. For all participants combined, across-channel GDTs and LBTs were positively and significantly correlated. This suggests that the 2 tasks may rely on a common across-channel temporal mechanism.