Cochlear Implantation in Patients with Mitochondrial Gene Mutation: Decline in Speech Perception in Retrospective Long-Term Follow-Up Study.
Kai KanemotoAkinori KashioErika OgataYusuke AkamatsuHajime KoyamaTsukasa UranakaYujiro HoshiShinichi IwasakiTatsuya YamasobaPublished in: Life (Basel, Switzerland) (2022)
Clinical evidence of the effectiveness of cochlear implantation for hearing loss with mitochondrial DNA mutation is limited. Most reports have only described short-term postoperative speech perception, which may not reflect the limitations of cochlear implantation caused by progressive retrocochlear dysfunction. The present study aimed to investigate long-term speech perception after cochlear implantation in patients with severe to profound hearing loss associated with mitochondrial DNA mutation. A retrospective chart review was performed on patients with mitochondrial DNA mutation who had undergone cochlear implantation at the Department of Otolaryngology and Head and Neck Surgery at the University of Tokyo Hospital. We extracted data on causative mutations, clinical types, clinical course, perioperative complications, and short-term and long-term postoperative speech perception. Nine patients with mitochondrial DNA mutation underwent cochlear implantation. The mean observation period was 5.5 ± 4.2 years (range, 1-13 years), and seven patients were followed for more than 3 years. Two of the seven patients who initially showed good speech perception exhibited deterioration during long-term follow-up. The absence of an acute progression of cognitive decline in patients, showing a gradual decrease in speech perception, suggests that the deterioration of speech perception was caused by progressive retrocochlear degeneration. Although most patients with mitochondrial DNA mutation maintained good speech perception for more than 3 years after cochlear implantation, retrocochlear degeneration could cause the deterioration of speech perception during long-term follow-up.
Keyphrases
- mitochondrial dna
- hearing loss
- copy number
- end stage renal disease
- cognitive decline
- patients undergoing
- chronic kidney disease
- newly diagnosed
- ejection fraction
- randomized controlled trial
- multiple sclerosis
- systematic review
- genome wide
- healthcare
- oxidative stress
- minimally invasive
- peritoneal dialysis
- mild cognitive impairment
- dna methylation
- machine learning
- emergency department
- risk factors
- autism spectrum disorder
- drug induced
- intensive care unit
- early onset
- gene expression
- liver failure
- big data
- acute coronary syndrome
- data analysis
- tertiary care