Dexamethasone-eluting cochlear implants reduce inflammation and foreign body response in human and murine cochleae

• Published in: Scientific reports Vol. 15; no. 1; pp. 30615 - 16
• Main Authors: Rahman, Muhammad Taifur, Mostaert, Brian J, Eckard, Peter, Fatima, Shakila Mahmuda, Scheperle, Rachel, Razu, Ibrahim, Hunger, Bryce, Olszewski, Rafal T., Gu, Shoujun, Garcia, Cristina L., Khan, Nashwaan Ali, Bennion, Douglas M, Oleson, Jacob, Kirk, Jonathon R., Enke, Ya Lang, Gay, Robert D., Morell, Robert J., Hirose, Keiko, Hoa, Michael, Claussen, Alexander D., Hansen, Marlan R.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 20.08.2025; Nature Publishing Group; Nature Portfolio
• Subjects: 631/250/256; 639/301/54/993; 692/308/575; Acoustics; Animal models; Clinical medicine; Cochlea; Cochlear implants; CX3CR1 protein; Dexamethasone; Electrical impedance; Electrodes; Energy consumption; Foreign bodies; Hearing loss; Hearing protection; Humanities and Social Sciences; Impedance; Inflammation; Macrophages; Middle ear; multidisciplinary; Science; Science (multidisciplinary); Silicones; Software; Transplants & implants
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-025-10739-y

The inflammatory foreign body response (FBR) following cochlear implantation (CI) can negatively impact CI outcomes, including increased electrode impedances. This study aims to investigate the long-term efficacy of dexamethasone-eluting cochlear implant and locally delivered dexamethasone, a potent anti-inflammatory glucocorticoid, on the intracochlear FBR and electrical impedance post-implantation in a murine model. Preliminary impedance data in humans are also provided as a complement to the murine data to illustrate generalizability and reinforce implications related to clinical application. The left ears of CX3CR1 +/GFP Thy1 +/YFP (macrophage-neuron dual reporter) mice were implanted with dexamethasone-eluting cochlear implants (Dex-CI) or standard implant (Standard-CI) while the right ear served as unoperated control. Another group of dual reporter mice was implanted with a standard CI electrode array followed by injection of dexamethasone in the middle ear to mimic current clinical practice (Dex-local). Mouse implants were electrically stimulated with serial measurements of electrical impedance. Human subjects were implanted with either standard or Dex-CI followed by serial impedance measurements. Dex-CI reduced electrical impedance in the murine model and human subjects and inflammatory FBR in the murine model for an extended period. Dex-local in the murine model is ineffective for long-term reduction of FBR and electrode impedance. Our data suggests that dexamethasone-eluting arrays are more effective than the current clinical practice of locally applied dexamethasone in reducing FBR and electrical impedance.