Skip to content
2000
Volume 20, Issue 1
  • ISSN: 1573-4056
  • E-ISSN: 1875-6603

Abstract

Background

The neural mechanisms underlying Congenital Sensorineural Hearing Loss (CSNHL) remain elusive.

Objective

This study evaluated the function of the glymphatic system in children with CSNHL compared to normal-hearing children using the DTI-ALPS approach, which utilizes diffusion tensor imaging along the perivascular space.

Methods

Twenty-six children with CSNHL and 30 age- and sex-matched Healthy Controls (HCs) with normal hearing thresholds were recruited. The DTI-ALPS index was calculated for each group. We analyzed the discrepancies in the DTI-ALPS index between patients with CSNHL and healthy controls. Additionally, Spearman's correlation analysis was performed to investigate the relationship between the DTI-ALPS index and age in children with CSNHL.

Results

Significant differences in the DTI-ALPS index were observed between the two groups. Compared with HCs, the DTI-ALPS index in CSNHL patients was significantly lower (1.49388±0.11441 . 1.61402±0.15430, =0.002). In addition, diffusivity along the z-axis in the association fiber (Dzzassoc) index was significantly higher in the CSNHL group than in the HC group (0.00041±0.00006 . 0.00036±0.00004, =0.003). Furthermore, we discovered a noteworthy downward correlation between the DTI-ALPS index and age in children with CSNHL (rho = -0.544, =0.005).

Conclusion

In this present study, glymphatic system activity in CSNHL children was investigated for the first time using the DTI-ALPS index. A significant decrease in glymphatic system function was detected in CSNHL children, which correlated well with age. The DTI-ALPS index could serve as a valuable biomarker for tracking disease progression and treatment in CSNHL and unraveling the neural mechanisms of early hearing deprivation in children with CSNHL.

This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: https://creativecommons.org/licenses/by/4.0/legalcode. This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Loading

Article metrics loading...

/content/journals/cmir/10.2174/0115734056305276240730113140
2024-01-01
2025-06-30
The full text of this item is not currently available.

References

  1. ShaveS. BottiC. KwongK. Congenital sensorineural hearing loss.Pediatr. Clin. North Am.202269222123410.1016/j.pcl.2021.12.00635337535
    [Google Scholar]
  2. TwomeyT. PriceC.J. WatersD. MacSweeneyM. The impact of early language exposure on the neural system supporting language in deaf and hearing adults.Neuroimage202020911641110.1016/j.neuroimage.2019.11641131857205
    [Google Scholar]
  3. BavelierD. TomannA. HuttonC. MitchellT. CorinaD. LiuG. NevilleH. Visual attention to the periphery is enhanced in congenitally deaf individuals.J. Neurosci.20002017RC9310.1523/JNEUROSCI.20‑17‑j0001.200010952732
    [Google Scholar]
  4. FiguerasB. EdwardsL. LangdonD. Executive function and language in deaf children.J. Deaf Stud. Deaf Educ.200813336237710.1093/deafed/enm06718252699
    [Google Scholar]
  5. BruceM. BellM.A. Vocabulary and executive functioning: A scoping review of the unidirectional and bidirectional associations across early childhood.Hum. Development202266316718710.1159/00052496436164662
    [Google Scholar]
  6. RasmussenM.K. MestreH. NedergaardM. The glymphatic pathway in neurological disorders.Lancet Neurol.201817111016102410.1016/S1474‑4422(18)30318‑130353860
    [Google Scholar]
  7. BeschornerN. NedergaardM. Glymphatic system dysfunction in neurodegenerative diseases.Curr. Opin. Neurol.202437218218810.1097/WCO.000000000000125238345416
    [Google Scholar]
  8. CiureaA.V. MohanA.G. Covache-BusuiocR.A. CostinH.P. SaceleanuV.M. The brain’s glymphatic system: Drawing new perspectives in neuroscience.Brain Sci.2023137100510.3390/brainsci1307100537508938
    [Google Scholar]
  9. CuiW. WangS. ChenB. FanG. White matter structural network alterations in congenital bilateral profound sensorineural hearing loss children: A graph theory analysis.Hear. Res.202242210852110.1016/j.heares.2022.10852135660126
    [Google Scholar]
  10. ParkK.H. ChungW.H. KwonH. LeeJ.M. Evaluation of cerebral white matter in prelingually deaf children using diffusion tensor imaging.BioMed Res. Int.201820181710.1155/2018/679539729511689
    [Google Scholar]
  11. JiangM. WenZ. LongL. WongC.W. YeN. ZeeC. ChenB.T. Assessing cerebral white matter microstructure in children with congenital sensorineural hearing loss: A tract-based spatial statistics study.Front. Neurosci.20191359710.3389/fnins.2019.0059731293368
    [Google Scholar]
  12. YangT. LiuQ. FanX. HouB. WangJ. ChenX. Altered regional activity and connectivity of functional brain networks in congenital unilateral conductive hearing loss.Neuroimage Clin.20213210281910.1016/j.nicl.2021.10281934537683
    [Google Scholar]
  13. CuiW. WangS. ChenB. FanG. Altered functional network in infants with profound bilateral congenital sensorineural hearing loss: A graph theory analysis.Front. Neurosci.20221581083310.3389/fnins.2021.81083335095404
    [Google Scholar]
  14. GuoP. LangS. JiangM. WangY. ZengZ. WenZ. LiuY. ChenB.T. Alterations of regional homogeneity in children with congenital sensorineural hearing loss: A resting-state fMRI study.Front. Neurosci.20211567891010.3389/fnins.2021.67891034690668
    [Google Scholar]
  15. XuK. ZhangJ. XingC. XuX. YinX. WuY. ChenX. ChenY.C. Evaluation of glymphatic system activity by diffusion tensor image analysis along the perivascular space in presbycusis.CNS Neurosci. Ther.2024303e1445810.1111/cns.1445837680170
    [Google Scholar]
  16. TaokaT. MasutaniY. KawaiH. NakaneT. MatsuokaK. YasunoF. KishimotoT. NaganawaS. Evaluation of glymphatic system activity with the diffusion MR technique: Diffusion tensor image analysis along the perivascular space (DTI-ALPS) in Alzheimer’s disease cases.Jpn. J. Radiol.201735417217810.1007/s11604‑017‑0617‑z28197821
    [Google Scholar]
  17. NaganawaS. TaokaT. ItoR. KawamuraM. The glymphatic system in humans: Investigations with magnetic resonance imaging.Invest. Radiol.202459111210.1097/RLI.000000000000096936897826
    [Google Scholar]
  18. LiangT. ChangF. HuangZ. PengD. ZhouX. LiuW. Evaluation of glymphatic system activity by diffusion tensor image analysis along the perivascular space (DTI-ALPS) in dementia patients.Br. J. Radiol.20239611462022031510.1259/bjr.2022031537066824
    [Google Scholar]
  19. ButlerT. ZhouL. OzsahinI. WangX.H. GarettiJ. ZetterbergH. BlennowK. JamisonK. de LeonM.J. LiY. KuceyeskiA. ShahS.A. Glymphatic clearance estimated using diffusion tensor imaging along perivascular spaces is reduced after traumatic brain injury and correlates with plasma neurofilament light, a biomarker of injury severity.Brain Commun.202353fcad13410.1093/braincomms/fcad13437188222
    [Google Scholar]
  20. QinY. LiX. QiaoY. ZouH. QianY. LiX. ZhuY. HuoW. WangL. ZhangM. DTI-ALPS: An MR biomarker for motor dysfunction in patients with subacute ischemic stroke.Front. Neurosci.202317113239310.3389/fnins.2023.113239337065921
    [Google Scholar]
  21. YehF.C. Shape analysis of the human association pathways.Neuroimage202022311732910.1016/j.neuroimage.2020.11732932882375
    [Google Scholar]
  22. LomberS.G. MeredithM.A. KralA. Cross-modal plasticity in specific auditory cortices underlies visual compensations in the deaf.Nat. Neurosci.201013111421142710.1038/nn.265320935644
    [Google Scholar]
  23. WangH.F. ZhangW. RollsE.T. LiY. WangL. MaY.H. KangJ. FengJ. YuJ.T. ChengW. Alzheimer’s Disease Neuroimaging Initiative.Hearing impairment is associated with cognitive decline, brain atrophy and tau pathology.EBioMedicine20228610433610.1016/j.ebiom.2022.10433636356475
    [Google Scholar]
  24. IshidaK. YamadaK. NishiyamaR. HashimotoT. NishidaI. AbeY. YasuiM. IwatsuboT. Glymphatic system clears extracellular tau and protects from tau aggregation and neurodegeneration.J. Exp. Med.20222193e2021127510.1084/jem.2021127535212707
    [Google Scholar]
  25. BuccellatoF.R. D’AncaM. SerpenteM. ArighiA. GalimbertiD. The role of glymphatic system in alzheimer’s and parkinson’s disease pathogenesis.Biomedicines2022109226110.3390/biomedicines1009226136140362
    [Google Scholar]
  26. BakkerE.N.T.P. BacskaiB.J. Arbel-OrnathM. AldeaR. BedussiB. MorrisA.W.J. WellerR.O. CarareR.O. Lymphatic clearance of the brain: Perivascular, paravascular and significance for neurodegenerative diseases.Cell. Mol. Neurobiol.201636218119410.1007/s10571‑015‑0273‑826993512
    [Google Scholar]
  27. LiY. BoothJ.R. PengD. ZangY. LiJ. YanC. DingG. Altered intra- and inter-regional synchronization of superior temporal cortex in deaf people.Cereb. Cortex20132381988199610.1093/cercor/bhs185
    [Google Scholar]
  28. SadatoN. YamadaH. OkadaT. YoshidaM. HasegawaT. MatsukiK.I. YonekuraY. ItohH. Age-dependent plasticity in the superior temporal sulcus in deaf humans: A functional MRI study.BMC Neurosci.2004515610.1186/1471‑2202‑5‑5615588277
    [Google Scholar]
  29. FriedmannN. RusouD. Critical period for first language: The crucial role of language input during the first year of life.Curr. Opin. Neurobiol.201535273410.1016/j.conb.2015.06.00326111432
    [Google Scholar]
/content/journals/cmir/10.2174/0115734056305276240730113140
Loading
/content/journals/cmir/10.2174/0115734056305276240730113140
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test