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Understanding speech in noisy settings is harder for hearing-impaired (HI) people than for normal-hearing (NH) people, even when speech is audible. This is often attributed to hearing loss altering the neural encoding of temporal and/or spectral speech cues. Here, we investigated whether this difference may also be due to an impaired ability to adapt to background noise. For 25 adult hearing-aid users with sensorineural hearing loss, speech reception thresholds (SRTs) were measured for natural and tone-vocoded words embedded in speech-shaped noise (SSN). The stimuli were preceded or not by a 1-second adapting SSN precursor. Adaptation was calculated as the difference in SRT between the two precursor conditions. Corresponding data for 28 NH listeners were taken from a previously published study. SRTs were worse for HI listeners, confirming that hearing loss diminishes access to speech acoustic cues. Furthermore, noise adaptation was negatively correlated with the age-controlled hearing loss both for natural (rho=-0.56, N = 52, p < 0.001) and vocoded (rho=-0.45, N = 39, p = 0.002) words. Impaired adaptation contributed up to 10% of the SRT loss in HI listeners. We conclude that HI listeners suffer from poorer speech in noise recognition not only because of impaired access to speech acoustic cues but also because they are less able to adapt to background noise.
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http://dx.doi.org/10.1038/s41598-024-80131-9 | DOI Listing |
Mol Genet Genomics
December 2024
ENT Institute and Department of Otorhinolaryngology, Eye & ENT Hospital, Fudan University, 83 Fen Yang Road, Shanghai, 200031, China.
Low-frequency non-syndromic hearing loss (LFNSHL) is a rare auditory disorder affecting frequencies ≤ 2000 Hz. To elucidate its genetic basis, we conducted whole-exome sequencing on nine Chinese families (31 affected individuals) with LFNSHL. Four heterozygous pathogenic variants, including two novel variants, were identified in common LFNSHL-related genes (WFS1, DIAPH1) and less common genes (TNC, EYA4), achieving a 44% genetic diagnosis rate.
View Article and Find Full Text PDFOtolaryngol Head Neck Surg
December 2024
Department of Otolaryngology-Head and Neck Surgery, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Objective: Despite certain studies indicating hearing impairments in individuals with polycystic ovary syndrome (PCOS), the correlation between PCOS and sensorineural hearing loss (SNHL) remains inconclusive. This study aimed to investigate the association between PCOS and SNHL.
Data Sources: A systematic literature search was conducted using PubMed, MEDLINE, EMBASE, and the Cochrane Library from inception to June 24, 2024.
Ear Nose Throat J
December 2024
Department of Otorhinolaryngology-Head and Neck Surgery, College of Medicine, Jeonbuk National University, Jeonju, Republic of Korea.
Pituitary macroadenomas are benign neoplasms that can cause a range of symptoms due to a mass effect on surrounding structures. This case report describes a 51-year-old male presenting with progressive bilateral hearing impairment and significant deterioration in speech discrimination over several years. Examination revealed normal tympanic membranes and no neurological deficits, while pure tone audiometry indicated mild to moderate sensorineural hearing loss.
View Article and Find Full Text PDFLancet Reg Health West Pac
December 2024
School of Biomedical Convergence Engineering, College of Information and Biomedical Engineering, Pusan National University, Yangsan, South Korea.
Background: Little is known about the impact of PM on people with disabilities. We aimed to explore the association between PM and hospitalization via the emergency department (ED admission) among people with disabilities, together with the attributable ED admission cases and costs.
Methods: We applied a time-stratified case-crossover design adjusting ozone, holiday, and temperature using seven years (2015-2021) of claim-based data on ED admissions from the Korean National Health Insurance Database.
World J Clin Oncol
December 2024
Department of Pathology, Peking University People's Hospital, Beijing 100044, China.
Background: Primary squamous cell carcinoma (SCC) of the middle ear is rare, with non-keratinizing basaloid types being exceptionally uncommon. Distinguishing these cancers, often caused by viral factors (, human papillomavirus or Epstein-Barr virus), or specific genetic alterations (, bromodomain-containing protein 4-nuclear protein in or gene fused with FLI chromosomal rearrangement), from other cranial conditions, is difficult. The recently identified DEK::AFF2 non-keratinizing SCC (NKSCC) is a novel subtype, fitting the World Health Organization classification of head and neck neoplasms.
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