Academic Journal

White Matter Tracts of the Auditory Pathways in Experimental Unilateral Ear Canal Atresia.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: White Matter Tracts of the Auditory Pathways in Experimental Unilateral Ear Canal Atresia.
Συγγραφείς: Siegbahn M; Department of Clinical Intervention and Technology, Division of ENT diseases, Karolinska Institute.; Department of Ear and Hearing, Karolinska University Hospital., Kraft Birkne S; Department of Biomedical Engineering and Health Systems, KTH Royal Institute of Technology., Maschio F; Department of Biomedical Engineering and Health Systems, KTH Royal Institute of Technology., Hultcrantz M; Department of Clinical Intervention and Technology, Division of ENT diseases, Karolinska Institute., Engmér Berglin C; Department of Clinical Intervention and Technology, Division of ENT diseases, Karolinska Institute.; Department of Otorhinolaryngology, Sophiahemmet Hospital, Stockholm, Sweden., Moreno R; Department of Biomedical Engineering and Health Systems, KTH Royal Institute of Technology.
Πηγή: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology [Otol Neurotol] 2026 Jul 01; Vol. 47 (6), pp. e868-e874. Date of Electronic Publication: 2026 Apr 15.
Τύπος έκδοσης: Journal Article
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 100961504 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-4505 (Electronic) Linking ISSN: 15317129 NLM ISO Abbreviation: Otol Neurotol Subsets: MEDLINE
Imprint Name(s): Original Publication: Hagerstown, MD : Lippincott Williams & Wilkins, c2001-
Ιατρικοί όροι (MeSH): Auditory Pathways*/pathology , White Matter*/pathology , White Matter*/diagnostic imaging , Ear Canal*/abnormalities , Ear Canal*/surgery , Hearing Loss, Conductive*/pathology , Hearing Loss, Unilateral*, Cochlear Nucleus/pathology ; Inferior Colliculi/pathology ; Ear/abnormalities ; Animals ; Rats ; Disease Models, Animal ; Diffusion Tensor Imaging ; Magnetic Resonance Imaging ; Male ; Diffusion Magnetic Resonance Imaging ; Congenital Abnormalities
Περίληψη: Hypothesis: Congenital unilateral conductive hearing impairment alters auditory white matter tract connections of the brain.
Background: Unilateral conductive hearing loss has negative effects on speech perception in noise and sound localization ability. This study examines auditory white matter tracts in a rat model with surgically induced unilateral ear canal atresia, compared with controls.
Materials and Methods: Twelve-month euthanized rats, 7 with left-sided surgically created ear canal atresia (UCA) and 4 controls, were scanned in a 9.4 T MRI scanner for animal research purposes. Diffusion-weighted images were acquired. Two different methods for probabilistic fiber tracking were used. Fractional anisotropy (FA) was calculated from whole brains and from tracts between defined auditory regions of interest.
Results: Both methods of fiber tracking show significantly higher global FA in rats with UCA. Within-group comparisons in UCA show higher FA on the hearing side between the cochlear nucleus and inferior colliculus, compared with the side of hearing loss, while in controls, there was no asymmetry. Lower FA was also found between the medial geniculate complex and the auditory cortex on the left side than on the right in UCA, in contrast to controls, where there was no difference between the hemispheres.
Conclusion: The asymmetry found in UCA indicates alterations of auditory white matter tracts as a response to asymmetric hearing, partly confirming previous findings in experiments on ferrets.
(Copyright © 2026, Otology & Neurotology, Inc.)
Competing Interests: The authors disclose no conflicts of interest.
References: Lieu JE. Speech-language and educational consequences of unilateral hearing loss in children. Arch Otolaryngol Head Neck Surg 2004;130:524–30.
Lieu JE. Unilateral hearing loss in children: speech-language and school performance. B-ENT 2013;21:107–15.
Kesser BW, Krook K, Gray LC. Impact of unilateral conductive hearing loss due to aural atresia on academic performance in children. Laryngoscope 2013;123:2270–5.
Jose MR, Mondelli MF, Feniman MR, Lopes-Herrera SA. Language disorders in children with unilateral hearing loss: a systematic review. Int Arch Otorhinolaryngol 2014;18:198–203.
Brookhouser PE, Worthington DW, Kelly WJ. Unilateral hearing loss in children. Laryngoscope 1991;101(12 pt 1):1264–72.
Liu Q, Wang Y, Yang T, et al. Poor speech recognition, sound localization and reorganization of brain activity in children with unilateral microtia-atresia. Brain Imaging Behav 2022;16:78–90.
Siegbahn M, Engmer Berglin C, Hultcrantz M, Asp F. Adults with unilateral congenital ear canal atresia - sound localization ability and recognition of speech in competing speech in unaided condition. Acta Otolaryngol 2021;141:689–94.
Rosenhall U. The influence of hearing loss on directional hearing. Scand Audiol 1985;14:187–9.
Agterberg MJ, Hol MK, Cremers CW, Mylanus EA, van Opstal J, Snik AF. Conductive hearing loss and bone conduction devices: restored binaural hearing? Adv Otorhinolaryngol 2011;71:84–91.
Kumpik DP, King AJ. A review of the effects of unilateral hearing loss on spatial hearing. Hear Res 2019;372:17–28.
Kelly JB, Judge PW, Fraser IH. Development of the auditory orientation response in the albino rat (Rattus norvegicus). J Comp Psychol 1987;101:60–66.
Coleman J, O’Connor P. Effects of monaural and binaural sound deprivation on cell development in the anteroventral cochlear nucleus of rats. Exp Neurol 1978;64:553–66.
Webster DB. Auditory neuronal sizes after a unilateral conductive hearing loss. Exp Neurol 1983;79:130–40.
Woolf NK, Sharp FR, Davidson TM, Ryan AF. Cochlear and middle ear effects on metabolism in the central auditory pathway during silence: a 2-deoxyglucose study. Brain Res 1983;274:119–27.
Tucci DL, Cant NB, Durham D. Effects of conductive hearing loss on gerbil central auditory system activity in silence. Hear Res 2001;155(1-2):124–32.
Tucci DL, Cant NB, Durham D. Conductive hearing loss results in a decrease in central auditory system activity in the young gerbil. Laryngoscope 1999;109:1359–71.
Moore DR, Hutchings ME, King AJ, Kowalchuk NE. Auditory brain stem of the ferret: some effects of rearing with a unilateral ear plug on the cochlea, cochlear nucleus, and projections to the inferior colliculus. J Neurosci 1989;9:1213–22.
Vale C, Juiz JM, Moore DR, Sanes DH. Unilateral cochlear ablation produces greater loss of inhibition in the contralateral inferior colliculus. Eur J Neurosci 2004;20:2133–40.
Hsu WC, Tzen KY, Huy PT, Duet M, Yeh TH. An animal model of central auditory pathway imaging in the rat brain by high resolution small animal positron emission tomography. Acta Otolaryngol 2009;129:423–8.
Popescu MV, Polley DB. Monaural deprivation disrupts development of binaural selectivity in auditory midbrain and cortex. Neuron 2010;65:718–31.
Liu J, Huang X, Zhang J. Unilateral conductive hearing loss disrupts the developmental refinement of binaural processing in the rat primary auditory cortex. Front Neurosci 2021;15:762337.
Baliyan V, Das CJ, Sharma R, Gupta AK. Diffusion weighted imaging: technique and applications. World J Radiol 2016;8:785–98.
Beaulieu C. The basis of anisotropic water diffusion in the nervous system - a technical review. NMR Biomed Nov-Dec 2002;15(7-8):435–55.
Mandonnet E, Sarubbo S, Petit L. The nomenclature of human white matter association pathways: proposal for a systematic taxonomic anatomical classification. Front Neuroanat 2018;12:94.
Zanin J, Dhollander T, Farquharson S, Rance G, Connelly A, Nayagam BA. Review: Using diffusion-weighted magnetic resonance imaging techniques to explore the microstructure and connectivity of subcortical white matter tracts in the human auditory system. Hear Res 2019;377:1–11.
Glendenning KK, Masterton RB. Comparative morphometry of mammalian central auditory systems: variation in nuclei and form of the ascending system. Brain Behav Evol 1998;51:59–89.
Geal-Dor M, Freeman S, Li G, Sohmer H. Development of hearing in neonatal rats: air and bone conducted ABR thresholds. Hear Res 1993;69(1-2):236–42.
McGinn M, Chole R, Henry K. Cholesteatoma induction. Consequences of external auditory canal ligation in gerbils, cats, hamsters, guinea pigs, mice and rats. Acta Otolaryngol 1984;97(3-4):297–304.
Rohlfing T. User Guide to the Computational Morphometry Toolkit. Version 1.20. Neuroscience Program, SRI International; 2011. Accessed October 1, 2020. https://www.nitrc.org/docman/view.php/212/708/UserGuideCMTK.pd.
Woolrich MW, Jbabdi S, Patenaude B, et al. Bayesian analysis of neuroimaging data in FSL. Neuroimage 2009;45(suppl 1):S173–86.
Yushkevich PA, Piven J, Hazlett HC, et al. User-guided 3D active contour segmentation of anatomical structures: significantly improved efficiency and reliability. Neuroimage 2006;31:1116–28.
George P, Watson C. The rat brain in stereotaxic coordinates, 4 edn. Elsevier; 1998.
Malmierca MS. The structure and physiology of the rat auditory system: an overview. Int Rev Neurobiol 2003;56:147–211.
Jenkinson M, Bannister P, Brady M, Smith S. Improved optimization for the robust and accurate linear registration and motion correction of brain images. Neuroimage 2002;17:825–41.
Shamir I, Assaf Y. Tutorial: a guide to diffusion MRI and structural connectomics. Nat Protoc 2025;20:317–35.
Piekarski DJ, Zahr NM, Zhao Q, et al. White matter microstructural integrity continues to develop from adolescence to young adulthood in mice and humans: same phenotype, different mechanism. Neuroimage Rep 2023;3:100179.
Tournier JD, Smith R, Raffelt D, et al. MRtrix3: a fast, flexible and open software framework for medical image processing and visualisation. Neuroimage 2019;202:116137.
Frigo M, Deslauriers-Gauthier S, Parker D, et al. Diffusion MRI tractography filtering techniques change the topology of structural connectomes. J Neural Eng 2020;17:10.1088.
Hain A, Jorgens D, Moreno R. Randomized iterative spherical-deconvolution informed tractogram filtering. Neuroimage 2023;278:120248.
Jörgens D, Descoteaux M, Moreno R. Challenges for Tractogram Filtering. In: Özarslan, E, Schultz, T, Zhang, E, Fuster, A. eds. Anisotropy Across Fields and Scales. Mathematics and Visualization. Springer, Cham. 2021. Accessed Febryary 11, 2021. https://doi.org/10.1007/978-3-030-56215-1_7.
Moseley ME, Cohen Y, Kucharczyk J, et al. Diffusion-weighted MR imaging of anisotropic water diffusion in cat central nervous system. Radiology 1990;176:439–45.
Shatil AS, Uddin MN, Matsuda KM, Figley CR. Quantitative ex vivo MRI changes due to progressive formalin fixation in whole human brain specimens: longitudinal characterization of diffusion, relaxometry, and myelin water fraction measurements at 3T. Front Med (Lausanne) 2018;5:31.
Wei J, Zhong W, Xiao C, Liu Y, Song C, Xiao Z. Selectivity of monaural synaptic inputs underlying binaural auditory information integration in the central nucleus of inferior colliculus. Front Cell Neurosci 2018;12:303.
Ono M, Oliver DL. The balance of excitatory and inhibitory synaptic inputs for coding sound location. J Neurosci 2014;34:3779–92.
Liu Y, Li Y, Peng Y, Yu H, Xiao Z. Bilateral interactions in the mouse dorsal inferior colliculus enhance the ipsilateral neuronal responses and binaural hearing. Front Physiol 2022;13:854077.
Clopton BM, Silverman MS. Changes in latency and duration of neural responding following developmental auditory deprivation. Exp Brain Res 1978;32:39–47.
Silverman MS, Clopton BM. Plasticity of binaural interaction. I. Effect of early auditory deprivation. J Neurophysiol 1977;40:1266–74.
Stuermer IW, Scheich H. Early unilateral auditory deprivation increases 2-deoxyglucose uptake in contralateral auditory cortex of juvenile Mongolian gerbils. Hear Res 2000;146(1-2):185–99.
Hutson KA, Durham D, Imig T, Tucci DL. Consequences of unilateral hearing loss: cortical adjustment to unilateral deprivation. Hear Res 2008;237(1-2):19–31.
Hackett TA. Information flow in the auditory cortical network. Hear Res 2011;271(1-2):133–46.
Kimura A, Imbe H, Donishi T. Efferent connections of an auditory area in the caudal insular cortex of the rat: anatomical nodes for cortical streams of auditory processing and cross-modal sensory interactions. Neuroscience 2010;166:1140–57.
Tao C, Zhang G, Zhou C, et al. Diversity in excitation-inhibition mismatch underlies local functional heterogeneity in the rat auditory cortex. Cell Rep 2017;19:521–31.
Jankowski MM, Karayanni M, Harpaz M, Polterovich A, Nelken I. A rapid anterior auditory processing stream through the insulo-parietal auditory field in the rat. J Neurosci 2025;45:e2382242025.
Games KD, Winer JA. Layer V in rat auditory cortex: projections to the inferior colliculus and contralateral cortex. Hear Res 1988;34:1–25.
Bajo VM, Nodal FR, Moore DR, King AJ. The descending corticocollicular pathway mediates learning-induced auditory plasticity. Nat Neurosci 2010;13:253–60.
Druga R, Syka J, Rajkowska G. Projections of auditory cortex onto the inferior colliculus in the rat. Physiol Res 1997;46:215–22.
Doucet JR, Molavi DL, Ryugo DK. The source of corticocollicular and corticobulbar projections in area Te1 of the rat. Exp Brain Res 2003;153:461–6.
Gordon K, Henkin Y, Kral A. Asymmetric hearing during development: the aural preference syndrome and treatment options. Pediatrics 2015;136:141–53.
Tillein J, Hubka P, Kral A. Monaural congenital deafness affects aural dominance and degrades binaural processing. Cereb Cortex 2016;26:1762–77.
Hubka P, Schmidt L, Tillein J, et al. Dissociated representation of binaural cues in single-sided deafness: implications for cochlear implantation. J Neurosci 2024;44:e1653232024.
Gordon KA, Deighton MR, Abbasalipour P, Papsin BC. Perception of binaural cues develops in children who are deaf through bilateral cochlear implantation. PLoS ONE 2014;9:e114841.
Vicente LC, Polonenko MJ, Gordon KA, Silva L, Costa OA, Alvarenga KF. Effects of sequential bilateral cochlear implantation in children: evidence from speech-evoked cortical potentials and tests of speech perception. Audiol Neurootol 2022;27:282–96.
Priwin C, Jonsson R, Magnusson L, Hultcrantz M, Granstrom G. Audiological evaluation and self-assessed hearing problems in subjects with single-sided congenital external ear malformations and associated conductive hearing loss. Int J Audiol 2007;46:162–71.
Kesser BW, Cole ED, Gray LC. Emergence of binaural summation after surgical correction of unilateral congenital aural atresia. Otol Neurotol 2016;37:499–503.
Viehweg R, Campbell RA. Localization difficulty in monaurally impaired listeners. Ann Otol Rhinol Laryngol 1960;69:622–34.
Kunst SJ, Leijendeckers JM, Mylanus EA, Hol MK, Snik AF, Cremers CW. Bone-anchored hearing aid system application for unilateral congenital conductive hearing impairment: audiometric results. Otol Neurotol 2008;29:2–7.
Siegbahn M, Engmer Berglin C, Moreno R. Automatic segmentation of the core of the acoustic radiation in humans. Front Neurol 2022;13:934650.
Grant Information: FoUI-988066 ALF
Contributed Indexing: Keywords: Central auditory pathways; MRI; Rats; Unilateral hearing loss
SCR Disease Name: Aural Atresia, Congenital
Entry Date(s): Date Created: 20260415 Date Completed: 20260612 Latest Revision: 20260612
Update Code: 20260613
DOI: 10.1097/MAO.0000000000004916
PMID: 41981746
Βάση Δεδομένων: MEDLINE
Περιγραφή
ISSN:1537-4505
DOI:10.1097/MAO.0000000000004916