Aims: To assess the maturational status of the brainstem auditory pathway in babies with apnoea of prematurity (AOP) at 33-34 weeks of postmenstrual age (PMA), an important time landmark at which AOP is resolved in most cases.
Study Design: Compare brainstem auditory maturation between very preterm babies with AOP and those without AOP (non-AOP) at the same PMA 33-34 weeks to define differences.
Results: The AOP group showed significantly longer latencies of waves III and V latency than the non-AOP group (p < 0.05 and 0.01). The I-V interval in the AOP group was significantly longer than in the non-AOP group (p < 0.001). The same was true for the I-III and III-V intervals (p < 0.001 and 0.05). Wave III amplitude was significantly smaller (p < 0.05), and wave V amplitude was moderately smaller than in the non-AOP. At PMA 33 weeks, waves III and V latencies and all intervals in the AOP group were significantly longer than in the non-AOP group (p < 0.05-0.001). At PMA 34 weeks, these wave latencies and intervals in the AOP group were still significantly longer than in the non-AOP group (p < 0.05-0.01). Wave III amplitude in the AOP group was significantly smaller at both PMA 33 and 34 weeks (p < 0.05 and 0.05).
Conclusions: Brainstem auditory maturation in AOP babies is delayed at PMA 33 weeks, and remains delayed at PMA 34 weeks. These findings highlight the importance of monitoring and adequate intervention strategies during PMA 33-34 weeks in AOP babies.
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http://dx.doi.org/10.1016/j.earlhumdev.2024.106164 | DOI Listing |
Worldwide, congenital deafness and pigmentation disorders impact millions with their diverse manifestations, and among these genetic conditions, mutations in the Microphthalmia-associated transcription factor (MITF: OMIM#156845) gene are notable for their profound effects on melanocyte development and auditory functions. This study reports a novel porcupine model exhibiting spontaneous deafness and pigmentation abnormalities reminiscent of human Waardenburg Syndrome Type 2 (WS2: OMIM#193510). Through phenotypic characterization, including coat color, skin, eye morphology, and auditory brainstem response (ABR) assessments, we identified hypopigmentation and complete deafness in mutant porcupines.
View Article and Find Full Text PDFInt J Pediatr Otorhinolaryngol
December 2024
Hacettepe University, Faculty of Medicine, Department of Opthalmology, Ankara, Turkey.
Aims And Objectives: This study aimed to investigate the presence, type, and severity of hearing losses in individuals with Duane Retraction Syndrome (DRS), and to ascertain if there are anomalies in the auditory pathways at the brainstem level in DRS, believed to arise from aberrant interaction between cranial nerves and brainstem nuclei.
Study Design: Cross-sectional observational study.
Setting: Tertiary referral centre.
Vestn Otorinolaringol
December 2024
St. Petersburg Research Institute of Ear, Throat, Nose and Speech, St. Petersburg, Russia.
Unlabelled: Central auditory disorders (CSD) - this is a violation of the processing of sound stimuli, including speech, above the cochlear nuclei of the brain stem, which is mainly manifested by difficulties in speech recognition, especially in noisy environments. Children with this pathology are more likely to have behavioral problems, impaired auditory, linguistic and cognitive development, and especially difficulties with learning at school.
Objective: To analyze the literature data on the epidemiology of central auditory disorders in school-age children.
Int J Numer Method Biomed Eng
January 2025
Department of Mechanical Science and Bioengineering, Graduate School of Engineering Science, Osaka University, Osaka, Japan.
In a previous study [H. Shintaku et al., Sensors and Actuators A: Physical 158 (2010): 183-192], an artificially developed auditory sensor device showed a frequency selectivity in the range from 6.
View Article and Find Full Text PDFInt J Pediatr Otorhinolaryngol
December 2024
Department of Otorhinolaryngology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
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