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- (Suraj et al., 2023)
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Normal linear and non-linear cochlear mechanisms and efferent system functioning in individuals with misophonia
Status:: #status/Bare-bones-review
Metadata
- Item Type: #journalArticle
- Authors:: Urs Suraj, Kavassery Venkateswaran Nisha, Prashanth Prabhu,
- Date Added: October 18, 2023
- URL: https://link.springer.com/10.1007/s00405-023-08273-6
- DOI: 10.1007/s00405-023-08273-6
- Cite Key: surajNormalLinearNonlinear2023
- Tags:: #Misophonia, #Bare-bones-review-🦴, #audiology, #Efferent-system, #Suppression, #Otoacoustic-emissions, #null-results,
- PDF Attachments
Abstract
| Background/Purpose | Background- • Misophonia not recognized as distinct disorder in DSM-V or ICD-11. • Multifaceted condition involving cognitive, emotional, and sensory processes. • Neuro-audiological model implicates abnormal auditory cortex activity, non-classical pathway, limbic system, and autonomic hyperactivation via classical conditioning. • Hypothesized pathophysiological overlap with tinnitus and hyperacusis. • Tinnitus literature shows abnormal/absent TEOAEs, lower DPOAE amplitudes, and altered MOCB function (hyperresponsive in tinnitus + hyperacusis). Purpose- • Assess linear OHC functioning in misophonia via TEOAEs. • Assess non-linear OHC functioning in misophonia via DPOAEs. • Assess auditory efferent (MOCB) functioning via contralateral suppression of TEOAEs and DPOAEs. |
| Participants/samples | • 40 ears with misophonia (20 participants; 2 male, 18 female). • 37 ears without misophonia (20 participants; 7 male, 13 female). • Age range 18–28 years. • Inclusion: normal hearing (<15 dB HL air/bone), 'A' type tympanogram, present ipsi/contralateral acoustic reflexes at 500/1000 Hz. • Exclusion: hearing loss, otologic deficits, neurological disorders, tinnitus, vestibular migraine, hyperacusis, musical training, hearing aid history. • Misophonia confirmed via Schröder et al. (2013) diagnostic criteria; severity via MAQ (mild and moderate only included). |
| Measures | • Pure-tone audiometry (air and bone conduction). • Tympanometry and acoustic reflexes. • MAQ (severity). • TEOAEs (global amplitude; band amplitudes at 1, 1.5, 2, 3, 4 kHz). • DPOAEs (band amplitudes at 1, 1.5, 2, 3, 4 kHz). • Contralateral suppression for both TEOAEs and DPOAEs. |
| Procedures | • Acoustically treated, electrically shielded room. • TEOAEs: non-linear pulse train clicks ~80 dB peak SPL, 80 μs duration, flat spectrum; reproducibility ≥80% required. • DPOAEs: f2/f1 = 1.22; L1 = 65 dB SPL, L2 = 55 dB SPL. • Contralateral suppression: white noise 50 dB SPL via insert earphone; suppression amplitude = OAE amplitude (no noise) − OAE amplitude (with noise). • ILO V6 system (Otodynamics) for OAE recording. |
| Results | • No group difference in TEOAE absolute amplitudes (global or band-specific). • No group difference in DPOAE absolute amplitudes across frequencies. • No group difference in TEOAE contralateral suppression amplitude at any frequency. • No group difference in DPOAE contralateral suppression amplitude at any frequency. |
| Discussion/Limits | Conclusion- • The findings indicate linear and non-linear OHC functioning is intact in misophonia. • The findings indicate MOCB efferent functioning in misophonia is comparable to controls. • The authors conclude the pathophysiology of misophonia is not related to cochlear or MOCB mechanisms. • The data support a more central locus for misophonia, possibly beyond the brainstem, consistent with prior cortical AEP, MMN, and fMRI evidence (diminished N1, reduced MMN, altered insula/ACC/amygdala/auditory cortex activity, greater ventral attention network connectivity). • The authors conclude misophonia, despite hypothesized overlap with tinnitus and hyperacusis, does not seem to share their peripheral inner ear or efferent involvement. |
| Limitations:: | • Only mild and moderate severity included; severe misophonia not represented. • Cognitive, psychological, and environmental contributors not assessed. |
| Future Directions:: | • Use auditory evoked potentials to probe central auditory processing. • Use functional neuroimaging to investigate central correlates. • Explore additional non-auditory contributors (cognitive, psychological, environmental). - [ ] |
| Relevance:: | • a rare example of published null results. was looking at some audiological things in the context of Misophonia but didn't find any differences between Misophonics and controls. |
Notes
key terms and concepts
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Misophonia – condition characterized by heightened sensitivity and strong emotional reactions to specific sounds; per Schröder et al. (2013), specific sounds (or anticipation of such sounds) immediately evoke feelings of irritation or disgust that escalate anger.
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TEOAEs (Transient Evoked Otoacoustic Emissions) – low level responses produced by OHCs following a brief acoustic stimulus (clicks/tone bursts); index linear OHC functioning.
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DPOAEs (Distortion Product Otoacoustic Emissions) – sounds emitted by OHCs in response to two simultaneous pure tones (f1, f2; f2/f1 = 1.22); index non-linear OHC functioning.
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MOCB (Medial Olivocochlear Bundle) – auditory efferent pathway; assessed via contralateral suppression of OAEs.
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Suppression amplitude – difference in OAE amplitude between conditions with and without contralateral noise stimulation.
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MAQ (Misophonia Assessment Questionnaire) – 21-item severity measure; mild (0–21), moderate (22–42), severe (43–63).
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Sex imbalance
- Misophonia group skewed strongly female (18F/2M); control more balanced (13F/7M). Not addressed analytically.
Severity restriction
- Severe misophonics excluded by recruitment outcome, not design — limits inference about whether peripheral effects might emerge at higher severity.
Tinnitus framing
- Authors lean heavily on tinnitus/hyperacusis as the comparison condition justifying peripheral hypothesis (Knudson et al., 2014 hyperresponsive MOCB in tinnitus+hyperacusis).
contextual statement
In a 2023 study, Suraj attempted to characterize peripheral cochlear and efferent auditory functioning in misophonia by recording TEOAEs, DPOAEs, and contralateral OAE suppression in 40 ears of normal-hearing individuals with mild-to-moderate misophonia and 37 control ears.
zettlekasten
Surja findings of normal audiological functioning in Misophonia