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DOI: 10.1055/s-0044-1791809
Diffusion Tensor Imaging of the Auditory Pathway in Prelingual Deaf Children in Comparison to Normal Hearing Children in the 1 to 7 Years of Age Group

Abstract
Objective This article aims to determine the microstructural alterations in the auditory pathway in prelingual deaf children using diffusion tensor imaging (DTI)-derived parameters—fractional anisotropy (FA) and apparent diffusion coefficient (ADC), and secondarily to evaluate these changes in rubella and cytomegalovirus (CMV) positive cases.
Materials and Methods A consecutive series of consenting deaf and normal children between 1 and 7 years of age, forming the case and control groups, respectively, underwent DTI, audiological tests, and testing for rubella, CMV, and toxoplasma infections. FA and ADC were measured at four locations bilaterally: lateral lemniscus (LL), inferior colliculus, medial geniculate body, and auditory cortex (AC).
Result The mean ADC values were higher and the mean FA values were lower in cases (19 males, 21 females, mean age 2.65 years) than the controls (21 males, 19 females, mean age 4.63 years) at all eight sites. Sixteen (40%), 17 (42.5%), and 7 (17.5%) cases had severe, severe to profound, and profound hearing loss, respectively, the FA and ADC values being significantly different for LL. For rubella and CMV immunoglobulin G, 20/40and 17/40 cases were positive, respectively, 11 for both, and none for toxoplasma. Significant decrease in FA was seen at LL and AC in rubella/CMV positive cases.
Conclusion Microstructural changes are seen throughout the auditory pathway in prelingual deaf children, especially with rubella and/or CMV positive status. Further studies may pave the path to segregate out patient groups potentially more responsive to cochlear implant.
Keywords
diffusion tensor imaging - prelingual deafness - auditory pathway - fractional anisotropy - apparent diffusion coefficientData Availability
The essential data pertaining to the study are attached in the [Supplementary File S1] (available in the online version).
Ethical Approval
This study was performed according to the Declaration of Helsinki, and after obtaining approval from the Institute Ethics Committee.
Publication History
Article published online:
24 October 2024
© 2024. Indian Radiological Association. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 Kral A, Sharma A. Developmental neuroplasticity after cochlear implantation. Trends Neurosci 2012; 35 (02) 111-122
- 2 Campbell R, MacSweeney M, Woll B. Cochlear implantation (CI) for prelingual deafness: the relevance of studies of brain organization and the role of first language acquisition in considering outcome success. Front Hum Neurosci 2014; 8: 834
- 3 Shaikh S, Kumar A, Bansal A. Diffusion tensor imaging: an overview. Neurol India 2018; 66 (06) 1603-1611
- 4 Wu CM, Ng SH, Wang JJ, Liu TC. Diffusion tensor imaging of the subcortical auditory tract in subjects with congenital cochlear nerve deficiency. AJNR Am J Neuroradiol 2009; 30 (09) 1773-1777
- 5 Miao W, Li J, Tang M. et al. Altered white matter integrity in adolescents with prelingual deafness: a high-resolution tract-based spatial statistics imaging study. AJNR Am J Neuroradiol 2013; 34 (06) 1264-1270
- 6 Huang L, Zheng W, Wu C. et al. Diffusion tensor imaging of the auditory neural pathway for clinical outcome of cochlear implantation in pediatric congenital sensorineural hearing loss patients. PLoS One 2015; 10 (10) e0140643
- 7 Chang Y, Lee SH, Lee YJ. et al. Auditory neural pathway evaluation on sensorineural hearing loss using diffusion tensor imaging. Neuroreport 2004; 15 (11) 1699-1703
- 8 Lin Y, Wang J, Wu C, Wai Y, Yu J, Ng S. Diffusion tensor imaging of the auditory pathway in sensorineural hearing loss: changes in radial diffusivity and diffusion anisotropy. J Magn Reson Imaging 2008; 28 (03) 598-603
- 9 Jiang M, Wen Z, Long L. et al. Assessing cerebral white matter microstructure in children with congenital sensorineural hearing loss: a tract-based spatial statistics study. Front Neurosci 2019; 13: 597
- 10 Park KH, Chung WH, Kwon H, Lee JM. Evaluation of cerebral white matter in prelingually deaf children using diffusion tensor imaging. BioMed Res Int 2018; 2018: 6795397
- 11 Shepherd RK, Hardie NA. Deafness-induced changes in the auditory pathway: implications for cochlear implants. Audiol Neurootol 2001; 6 (06) 305-318
- 12 Leuridan E, Van Damme P. Passive transmission and persistence of naturally acquired or vaccine-induced maternal antibodies against measles in newborns. Vaccine 2007; 25 (34) 6296-6304
- 13 Leuridan E, Hens N, Hutse V, Aerts M, Van Damme P. Kinetics of maternal antibodies against rubella and varicella in infants. Vaccine 2011; 29 (11) 2222-2226
- 14 Kiliç A, Altinkaynak S, Ertekin V, Inandi T. The duration of maternal measles antibodies in children. J Trop Pediatr 2003; 49 (05) 302-305
- 15 Niewiesk S. Maternal antibodies: clinical significance, mechanism of interference with immune responses, and possible vaccination strategies. Front Immunol 2014; 5: 446
- 16 Nijman J, Gunkel J, de Vries LS. et al. Reduced occipital fractional anisotropy on cerebral diffusion tensor imaging in preterm infants with postnatally acquired cytomegalovirus infection. Neonatology 2013; 104 (02) 143-150
- 17 van der Voorn JP, Pouwels PJ, Vermeulen RJ, Barkhof F, van der Knaap MS. Quantitative MR imaging and spectroscopy in congenital cytomegalovirus infection and periventricular leukomalacia suggests a comparable neuropathological substrate of the cerebral white matter lesions. Neuropediatrics 2009; 40 (04) 168-173
- 18 Xia W, Yan H, Zhang Y. et al. Congenital human cytomegalovirus infection inducing sensorineural hearing loss. Front Microbiol 2021; 12: 649690
- 19 Cohen BE, Durstenfeld A, Roehm PC. Viral causes of hearing loss: a review for hearing health professionals. Trends Hear 2014; 18: 2331216514541361