# Etiology-Driven Personalized Cochlear Implantation: Implications for Electrode Choice, Timing, and Outcomes

**Authors:** Chang-Hee Kim, Byung Yoon Choi

PMC · DOI: 10.3390/jpm16030130 · 2026-02-28

## TL;DR

This paper argues that cochlear implantation should be personalized based on the cause of hearing loss to improve outcomes.

## Contribution

The paper introduces the concept of etiology-driven personalization in cochlear implantation decisions.

## Key findings

- Etiology impacts neural survival, cochlear anatomy, and auditory plasticity, affecting implant outcomes.
- Tailoring implant strategies to specific causes of hearing loss may reduce variability in patient outcomes.
- Cochlear implantation should be considered a precision intervention rather than a uniform procedure.

## Abstract

Background/Objectives: A Cochlear implantation (CI) is well-established auditory rehabilitation for severe to profound sensorineural hearing loss (SNHL), yet outcomes vary widely among implantees. Even with advancements in surgical methods and device technology, CI is still commonly applied as a generally uniform procedure, with limited attention to the underlying cause of SNHL. This review aims to summarize current evidence supporting etiology-based personalization of CI and to examine how etiology influences electrode selection, implantation timing, and clinical outcomes. Methods: We reviewed clinical and translational studies focusing on congenital cytomegalovirus infection, genetic hearing loss, cochlear nerve deficiency, and inner-ear malformations, emphasizing how etiology influences cochlear anatomy, neural integrity, and CI outcomes. Results: Etiology significantly affects neural survival, cochlear anatomy, and auditory plasticity, all of which influence optimal electrode design, insertion strategy, and timing of CI. Tailoring CI approaches to specific etiologies may help explain the substantial variability in outcomes observed in both children and adults. Conclusions: CI should be viewed as a precision-based intervention rather than a uniform treatment. Integrating etiology into clinical decision-making is essential for advancing truly personalized CI.

## Linked entities

- **Diseases:** sensorineural hearing loss (MONDO:0010576)

## Full-text entities

- **Genes:** COCH (cochlin) [NCBI Gene 1690] {aka COCH-5B2, COCH5B2, DFNA9, DFNB110}, POU3F4 (POU class 3 homeobox 4) [NCBI Gene 5456] {aka BRAIN-4, BRN-4, BRN4, DFN3, DFNX2, OCT-9}, SLC26A4 (solute carrier family 26 member 4) [NCBI Gene 5172] {aka DFNB4, EVA, PDS, TDH2B}, GJB2 (gap junction protein beta 2) [NCBI Gene 2706] {aka BAPS, CX26, DFNA3, DFNA3A, DFNB1, DFNB1A}, PCDH15 (protocadherin related 15) [NCBI Gene 65217] {aka CDHR15, DFNB23, USH1F}, KCNQ4 (potassium voltage-gated channel subfamily Q member 4) [NCBI Gene 9132] {aka DFNA2, DFNA2A, KV7.4}, OTOF (otoferlin) [NCBI Gene 9381] {aka AUNB1, DFNB6, DFNB9, FER1L2, NSRD9}
- **Diseases:** Otosclerosis (MESH:D010040), sensory disorders (MESH:D012678), SNHL (MESH:D006319), IP I-III (MESH:C538435), apical trauma (MESH:D014947), Meniere's disease (MESH:D008575), hearing decline (MESH:D060825), Congenital infections (MESH:D007239), inner ear inflammation (MESH:D010031), IP (MESH:C536298), HL (MESH:C538324), synaptic or neural dysfunction (MESH:C536122), neural canal stenosis (MESH:D003251), Labyrinthitis ossificans (MESH:D007762), IEMs (MESH:D007759), cognitive decline (MESH:D003072), prolonged auditory deprivation (MESH:D008133), CI (MESH:D015834), CND (MESH:C535376), congenital (MESH:D008209), ANSD (MESH:D006311), cCMV (MESH:D003586), X-linked anomaly (MESH:C564433), ossification (MESH:C562735), VS (MESH:D009464), Disorders (MESH:D009358), central nervous system abnormalities (MESH:D063647), DFNB9 (MESH:C563396), auditory deprivation (MESH:D012892), residual hearing (MESH:D018365), middle ear disease (MESH:D010033), COCH-related disease (MESH:D000077733), aplasia (MESH:C536482), meningitis (MESH:D008580), OTOF-related auditory neuropathy (MESH:C538268), fibrosis (MESH:D005355), Deafness (MESH:D003638), presbycusis (MESH:D011304), CSF leak (MESH:D002559), age-related hearing loss (MESH:D010024), cochlear nerve deficiency (MESH:D000160), related (MESH:D019973), Malformations (MESH:C564254), impaired communication (MESH:D003147), Hearing Loss (MESH:D034381), neural degeneration (MESH:D009410), auditory pathway abnormalities (MESH:D001304), spiral ganglion degeneration (MESH:D050723), inflammation (MESH:D007249)
- **Chemicals:** luminal (MESH:D010634), hyaluronic acid (MESH:D006820), dexamethasone (MESH:D003907)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** m.1555A > G, p.Pro51Ser, m.3243A > G, p.V37I

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Source: https://tomesphere.com/paper/PMC13027404