Deep Phenotyping of Hearing Instability Disorders: Cohort Establishment, Biomarker Identification, Development of Novel Phenotyping Measures, and Discovery of Therapeutic Targets
Purpose
Background: Disorders of hearing instability (HI) are poorly characterized and ineffectively treated. HI can cause fluctuations in hearing thresholds and speech understanding. Researchers want to use a specialized form of magnetic resonance imaging (MRI) and blood tests to learn more about HI. Objective: To characterize a cohort of people with HI and to correlate HI with other data, including hearing evaluations, as well as radiologic and immunologic biomarkers of inflammation over time. Eligibility: Adults ages 18-80 who have symptoms consistent with possible HI. Design: Participants will be screened with a medical and hearing history and medical record review. Participants will have physical exams. Their head and neck will be examined. They will have blood drawn. Participants will have hearing tests. They will wear headphones or foam earplugs. They will listen to different tones. They may describe what they hear. Participants will have balance tests. They will wear goggles as they watch moving lights or while cold or warm air is blown into their ears. They will sit in a spinning chair in a quiet, dark booth. From a reclining position, they will raise their head while clicking sounds are played into their ears. Participants will have MRIs of the inner ear and brain. The MRI scanner is a metal cylinder surrounded by a strong magnetic field. During the MRIs, participants will lie on a table that slides in and out of the scanner. Soft padding or a coil will be placed around their head. They will get a contrast agent through an intravenous catheter. Participation will last up to 15 months. ...
Conditions
- Meniere's Disease
- Enlarged Vestibular Aqueduct Syndrome
- Autoimmune Inner Ear Disease
Eligibility
- Eligible Ages
- Between 18 Years and 80 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- Yes
Criteria
- NCLUSION CRITERIA:
Affected Adults
In order to be eligible to participate in this study as a subject with HI, an individual
must meet all of the following criteria:
1. Provision of signed and dated informed consent.
2. Stated willingness to comply with all study procedures and availability for the
duration of the study
3. All genders, aged 18-80 years
Diagnosed with hearing instability, defined as documented hearing instability on
serial audiometry with sensorineural hearing loss (SNHL) greater than 30 dB HL at
one or more frequencies on at least one hearing test. Inclusion will require
documentation of clinically significant change in hearing (either worsening or
improvement) between at least 2 hearing tests or documentation of a sudden change in
hearing. Clinically significant change in hearing will be defined by a change of10
dB at any three frequencies, 15 dB at any two frequencies, or at least 20 dB at one
frequency. A sudden change in hearing will be defined as at least a 30 dB difference
at 3 consecutive frequencies in the affected ear as compared to the contralateral
ear.
4. No air-bone gaps in excess of 10 dB for 500-4000 Hz indicative of conductive HL in
at least 1 ear.
5. For females of reproductive potential: Negative pregnancy test at start of study
Unaffected Adults
In order to be eligible to participate in this study as a healthy volunteer, an
individual must meet all of the following criteria:
1. Provision of signed and dated informed consent.
2. Stated willingness to comply with all study procedures and availability for the
duration of the study
3. All genders, aged 18-80 years
4. No air-bone gaps in excess of 10 dB for 500-4000Hz indicative of conductive HL in at
least one ear.
5. Normal middle ear function as indicated by normal 226 Hz tympanograms bilaterally,
defined as middle ear pressure between plus minus 100 decaPascals, and peak
compensated static compliance between 0.3-1.8 milliliters
6. For females of reproductive potential: Negative pregnancy test at start of study
EXCLUSION CRITERIA:
Affected and unaffected individuals who meet any of the following criteria will be
excluded from participation in this study:
1. Presence of non-MRI compatible devices (cardiac pacemaker, meta<specific devices
(e.g., cardiac pacemaker)
2. Pregnancy or lactation
3. Known allergic reactions to gadolinium
4. Febrile illness within 2 weeks that could affect immune profiling*
5. Evidence of active outer or middle ear disease or anomaly (e.g. otitis media,
stenotic ear canal, otorrhea)
6. History of chronic, as defined by fluid in the middle ear for more than 4 months, or
recurrent otitis media, as defined by more than 4 episodes of acute otitis media in
one year.
7. Current PE tubes
8. Bilateral profound (Pure tone average (PTA) > 90 dB HL) sensorineural hearing loss
9. History or diagnosis of a central nervous system disorder, including but not limited
to:
1. Intracranial tumors
2. Cerebrovascular disease
3. Degenerative CNS disorder
4. CNS trauma
5. Encephalitis
6. Meningitis
10. Unable to discontinue medications that can interfere with vestibular test results
for the 48 hours immediately preceding a vestibular study session. These include any
and all anti-dizziness medications (such as Antivert), alcohol, caffeine,
prescription pain medications (such as Percocet), prescription headache medications
(such as Imitrex), sleeping pills (such as Ambien), anti-seizure medications (such
as Topamax), and/or antihistamines (such as Benadryl).
11. Current diagnosis from the Diagnostic and Statistical Manual of Mental Disorders
(DSM IV) of schizophrenia, bipolar disorder, or psychosis.
12. Unstable intercurrent illness that in the judgment of the PI could prevent or
confound collection of data.
Prospective study subjects who are cognitively impaired and lack consent capacity, will
not be enrolled.
*Participants suspected of having COVID-19 will be moved to the designated COVID-19 unit
and tested for SARS CoV-2 and Respiratory Pathogen Panel per guidance from NIH CC
Clinical Practice Safety Guidelines. Possible COVID-19 infections identified by phone
screen will not be eligible for study protocol until infection resolved.
Study Design
- Phase
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
| 1/All Patients | Documented hearing instability |
Recruiting Locations
Bethesda, Maryland 20892
For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR)
800-411-1222
prpl@cc.nih.gov
More Details
- Status
- Recruiting
- Sponsor
- National Institute on Deafness and Other Communication Disorders (NIDCD)
Detailed Description
Study Description: Disorders of hearing instability remain poorly characterized, phenotyped and ineffectively treated, and may result in sudden changes in hearing. These disorders include, but are not limited to, sudden sensorineural hearing loss (SSNHL) as well as hearing fluctuation, including, but not limited to, autoimmune inner ear disease (AIED), Meniere s disease (MD) and enlarged vestibular aqueduct syndrome (EVAS). While this group of disorders is likely to be clinically and etiologically heterogeneous, a common feature is fluctuation of hearing thresholds and speech understanding as measured by word recognition scores (WRS). This protocol seeks to ascertain a cohort of patients with hearing fluctuation to correlate these main phenotypic features with other phenomic data including audiometric indicators of endolymphatic hydrops as well as radiologic and immunologic biomarkers of inflammation over time. The overall hypothesis is that phenomic data will enable stratification of the phenotype of patients with hearing instability disorders. Healthy volunteers will be recruited to establish the normative range of endolymph and perilymph on contrast-enhanced delayed FLAIR MRI to allow for quantitative computational analysis of contrastenhanced delayed FLAIR MRI images. Objectives: Primary objective: To develop a cohort of patients with hearing instability (HI). Secondary objectives: 1. To correlate evidence of HI with changes in phase-shift distortion product otoacoustic emissions (DPOAEs). 2. To compare phase-shift DPOAEs to existing measures of auditory function including word recognition score (WRS), standard DPOAEs, and electrocochleography (ECochG) over time. 3. To compare phase-shift DPOAEs to vestibular measures including cervical and ocular vestibular evoked myogenic potentials (VEMPs) over time. 4. To correlate auditory and vestibular indicators of hearing instability and endolymphatic hydrops (EH) on MRI with quantitative differences in immunologic markers of inflammation over time. 5. Establish the normative range of endolymph and perilymph volume on contrast-enhanced delayed FLAIR MRI to allow for quantitative computational analysis of contrast-enhanced delayed FLAIR MRI images Exploratory objective: 1. To stratify patients with hearing instability (HI) by differences in cytokine levels, which will inform the identification of clinical subtypes of HI and potentially identify therapeutic targets for future treatment with targeted agents. 2. To perform transcriptional and immunoprofiling of PBMCs at time points associated with hearing fluctuation from phenotyped patient cohorts. Endpoints: Primary Endpoint: Identification of phenomic features associated with HI. Secondary Endpoint: (1) Identification of a variety of phenomic features of patients with HI that allow assignment to clinical subdivisions. Exploratory Endpoints 1. Identification of potential targets for therapeutics based on longitudinal immune/transcriptional profiling of patients with hearing instability. 2. Identification of subtype-specific immune cell distributions 3. Identification of immune profiles as well as immune cell transcriptional profiles related to hearing fluctuation