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1.
Sci Rep ; 14(1): 18344, 2024 08 07.
Artigo em Inglês | MEDLINE | ID: mdl-39112560

RESUMO

To evaluate the genetics of chronic nonsuppurative otitis media (OM). We performed a genome-wide association study of 429,599 individuals included in the FinnGen study using three different case definitions: combined chronic nonsuppurative OM (7034 cases) (included serous and mucous chronic OM), mucous chronic OM (5953 cases), and secretory chronic OM (1689 cases). Individuals without otitis media were used as controls (417,745 controls). We used immunohistochemistry (IHC) of the murine middle ear to evaluate the expression of annexin A13. Four loci were significantly associated (p < 1.7 × 10-8) with nonsuppurative OM. Three out of the four association signals included missense variants in genes that may play a role in otitis media pathobiology. According to our subtype-specific analyses, one novel locus, located near ANXA13, was associated with secretory OM. Three loci (near TNFRSF13B, GAS2L2, and TBX1) were associated with mucous OM. Immunohistochemistry of murine middle ear samples revealed annexin A13 expression at the apical pole of the Eustachian tube epithelium as well as variable intensity of the secretory cells of the glandular structure in proximity to the Eustachian tube. We demonstrated that secretory and mucous OM have distinct and shared genetic associations. The association of GAS2L2 with ciliary epithelium function and the pathogenesis of dysfunctional mucosa in mucous OM is suggested. The abundant expression of annexin A13 in the Eustachian tube epithelium, along with its role in apical transport for the binding and transfer of phospholipids, indicates the role of annexin A13 and phospholipids in Eustachian tube dysfunction.


Assuntos
Anexinas , Estudo de Associação Genômica Ampla , Otite Média , Animais , Anexinas/genética , Anexinas/metabolismo , Humanos , Camundongos , Otite Média/genética , Otite Média/metabolismo , Otite Média/patologia , Feminino , Masculino , Orelha Média/metabolismo , Orelha Média/patologia , Polimorfismo de Nucleotídeo Único , Predisposição Genética para Doença , Tuba Auditiva/patologia , Tuba Auditiva/metabolismo
2.
Cochlear Implants Int ; 21(3): 153-159, 2020 05.
Artigo em Inglês | MEDLINE | ID: mdl-32160829

RESUMO

Objectives: To investigate the effect of fixed and adaptive microphone directionality on speech reception threshold (SRT) in noise when compared to omnidirectional mode in unilateral cochlear-implant (CI) use for three different CI systems.Methods: Twenty-four CI recipients with bilateral severe-to-profound hearing loss participated in the study. Eight recipients of each CI system were enrolled, and their SRT in noise was measured when the speech and noise signals were co-located in the front to serve as a baseline. The acute effect of different microphone directionalities on SRT in noise was measured with the noise emanating at 90° in the horizontal plane from the side of the CI sound processor (S0NCI).Results: When compared to the baseline condition, the individual data revealed fairly similar patterns within each CI system. In the S0NCI condition, the average improvement in SRT in noise for fixed and adaptive directionalities over the omnidirectional mode was statistically significant and ranged from 1.2 to 6.0 dB SNR and from 3.7 to 12.7 dB SNR depending on the CI system, respectively.Discussion: Directional microphones significantly improve SRT in noise for all three CI systems. However, relatively large differences were observed in the directional microphone efficacy between CI systems.


Assuntos
Implante Coclear/instrumentação , Implantes Cocleares , Surdez/psicologia , Desenho de Prótese/psicologia , Percepção da Fala/fisiologia , Adulto , Surdez/cirurgia , Feminino , Humanos , Masculino , Teste de Materiais , Pessoa de Meia-Idade , Ruído , Período Pós-Operatório , Teste do Limiar de Recepção da Fala
3.
Acta Otolaryngol ; 136(10): 1035-40, 2016 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-27121373

RESUMO

OBJECTIVES: The aim of the study was to develop a reliable and easily accessible screening test for primary detection of hearing impairment. METHODS: Digits 0-9 were used to form quasirandom digit triplets. First, digit specific intelligibility functions and speech recognition thresholds (SRTs) were determined. To homogenize the test material digits with steep intelligibility function slopes were chosen and level correction up to ±2 dB were applied to the digits as needed. Evaluation measurements were performed to check for systematic differences in intelligibility between the test lists and to obtain normative reference function for normal-hearing listeners. RESULTS: The mean SRT and the final slope of the test lists were -10.8 ± 0.1 dB signal-to-noise ratio (SNR) and 21.7 ± 1.8%/dB, respectively (measurements at constant level; inter-list variability). The mean SRT and slope of the test subjects were -10.8 ± 0.5 dB SNR and 23.4 ± 5.2%/dB (measurements at constant level; inter-subject variability). The mean SRT for normal-hearing young adults for a single adaptive measurement is -9.8 ± 0.9 dB SNR. CONCLUSION: The Finnish digit triplet test is the first self-screening hearing test in the Finnish language. It was developed according to current standards, and it provides reliable and internationally comparable speech intelligibility measurements.


Assuntos
Perda Auditiva/diagnóstico , Programas de Rastreamento/métodos , Adolescente , Adulto , Voluntários Saudáveis , Testes Auditivos , Humanos , Padrões de Referência , Adulto Jovem
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