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Tinnitus and tinnitus disorder: Genetic, neurobiological, and clinical differentiation
Journal article   Open access   Peer reviewed

Tinnitus and tinnitus disorder: Genetic, neurobiological, and clinical differentiation

Dirk De Ridder, Tobias Kleinjung, Jae-Jin Song, Divya Adhia, Matt Hall, Anusha Yasoda-Mohan, Sven Vanneste, Alain Londero, Nathan Weisz, Winfred Schlee, …
iScience, Vol.29(6), 116080
03/06/2026
Handle:
https://hdl.handle.net/10523/51322

Abstract

behavioral neuroscience clinical neuroscience genetics psychiatry
Tinnitus is the conscious perception of sound in the absence of an external acoustic source. When accompanied by emotional distress, cognitive dysfunction, or autonomic arousal leading to behavioral and functional impairment, it is termed “tinnitus disorder.” This perspective synthesizes genetic, epidemiological, and neuroimaging evidence supporting the distinction between tinnitus and tinnitus disorder. Genetic studies indicate that tinnitus is linked to multiple common variants of small effect size, whereas tinnitus disorder involves rarer variants exerting larger effects. Epidemiologically, hearing loss is the primary risk factor for tinnitus, whereas personality traits like neuroticism, mood, and sleep disturbances predict tinnitus disorder. Neuroimaging identifies three interrelated neural pathways: a lateral “loudness” pathway, a descending “inhibitory” pathway, and a medial “distress” pathway that is specifically activated in tinnitus disorder, providing a neural basis for tinnitus related suffering. Future needs include the establishment of standardized diagnostic criteria and a severity grading system of tinnitus disorder.
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Published (Version of record) Open Access CC BY V4.0
url
https://doi.org/10.1016/j.isci.2026.116080View
Published (Version of record) Open CC BY V4.0

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