Evidence map›Paper›PMID 34054423›Full record

ArticleFrontiers in neuroscience2021

Comparison of Age-Related Pigmentary Changes in the Auditory and Vestibular Systems Within Mouse and Human Temporal Bones.

Nicholas S Andresen, Sarah Coreas, Dillan F Villavisanis, Amanda M Lauer

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Article in Frontiers in neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Nicholas S AndresenDepartment of Otolaryngology - Head & Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Sarah CoreasDepartment of Otolaryngology - Head & Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Dillan F VillavisanisIcahn School of Medicine at Mount Sinai, New York, NY, United States.
Amanda M LauerDepartment of Otolaryngology - Head & Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

Funding

RESEARCH TRAINING IN OTOLARYNGOLOGYT32DC000027 · NIDCD · JOHNS HOPKINS UNIVERSITY · PI CAREY, JOHN PATRICK · 1989 to 2023
$5.5M
Supplement for temporal bone tissue scanning equipmentR01DC016641 · NIDCD · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI DENT, MICHEAL L, LAUER, AMANDA M. · 2018 to 2022
$2.2M
NIDCD NIH HHS R01 DC016641NIDCD NIH HHS T32 DC000027
6 · The paper itself

Abstract

backgroundMelanin pigmentation is present within the auditory and vestibular systems of the mammalian inner ear and may play a role in maintaining auditory and vestibular function. Melanocytes within the stria vascularis (SV) are necessary for the generation of the endocochlear potential (EP) and decreased EP has been linked to age-related hearing loss. Melanocytes and pigment-containing "dark cells" are present within the vestibular system, but have a less well-defined role. African-American individuals have increased pigmentation within the SV and vestibular system, which is hypothesized to be related to lower rates of age-related hearing loss and vestibular dysfunction. It remains unclear if increased pigmentation confers lifelong protection against hearing loss and vestibular dysfunction.

methodsMouse temporal bones were collected from juvenile (3-4 week) and aged (20-32 months) CBA/CaJ mice. Pediatric and adult human temporal bones from Caucasian or African-American individuals were examined from the Johns Hopkins Temporal Bone Collection. Information regarding Fitzpatrick skin type were unavailable, and self-identified race/ethnicity was used as a proxy. Images were taken using light microscopy at 20× magnification. ImageJ software (v1.53) was used to measure pigment within the SV and vestibular system.

resultsIn mouse temporal bones pigmentation within the SV increased with age, but pigmentation within the vestibular system did not increase with age. In human temporal bones pigmentation within the SV increased with age and pigmentation within the vestibular system increased within the wall of the utricle, but not other regions of the vestibular system. African-American individuals had higher amounts of pigment within the SV and vestibular system, among both pediatric and adult populations.

conclusionStria vascularis pigmentation increases with age in mouse and human temporal bones. Pigmentation within the vestibular system did not increase with age in mouse specimens and only increased within the utricular wall with age in human specimens. Individuals who identified as African-American had higher pigment content within the SV and vestibular system, both as children and as adults. These results highlight how similar age-related pigmentary changes occur in the auditory and vestibular systems across species and underscore the importance of racial/ethnic diversity in human temporal bone studies.

Indexed as

age-related hearing lossauditorycochleamelaninpigmentationvestibular

Identifiers

PMID34054423
PMCPMC8163230

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