Genetic architecture distinguishes tinnitus from hearing loss.
Royce E CliffordAdam X MaihoferChris ChatzinakosJonathan R I ColemanNikolaos P DaskalakisMarianna GasperiKelleigh HoganElizabeth A MikitaMurray B SteinCatherine TcheandjieuFrancesca TeleseYanning ZuoAllen F RyanCaroline M NievergeltPublished in: Nature communications (2024)
Tinnitus is a heritable, highly prevalent auditory disorder treated by multiple medical specialties. Previous GWAS indicated high genetic correlations between tinnitus and hearing loss, with little indication of differentiating signals. We present a GWAS meta-analysis, triple previous sample sizes, and expand to non-European ancestries. GWAS in 596,905 Million Veteran Program subjects identified 39 tinnitus loci, and identified genes related to neuronal synapses and cochlear structural support. Applying state-of-the-art analytic tools, we confirm a large number of shared variants, but also a distinct genetic architecture of tinnitus, with higher polygenicity and large proportion of variants not shared with hearing difficulty. Tissue-expression analysis for tinnitus infers broad enrichment across most brain tissues, in contrast to hearing difficulty. Finally, tinnitus is not only correlated with hearing loss, but also with a spectrum of psychiatric disorders, providing potential new avenues for treatment. This study establishes tinnitus as a distinct disorder separate from hearing difficulties.
Keyphrases
- hearing loss
- genome wide
- copy number
- systematic review
- healthcare
- magnetic resonance
- gene expression
- dna methylation
- magnetic resonance imaging
- computed tomography
- climate change
- quality improvement
- genome wide association study
- genome wide identification
- human health
- subarachnoid hemorrhage
- genome wide association