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Association of Age Related Macular Degeneration and Age Related Hearing Impairment
PURPOSE: To evaluate the association between age-related macular degeneration (ARMD) and sensory neural hearing impairment (SHI). METHODS: In this case-control study, hearing status of 46 consecutive patients with ARMD were compared with 46 age-matched cases without clinical ARMD as a control group....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4860988/ https://www.ncbi.nlm.nih.gov/pubmed/27195086 http://dx.doi.org/10.4103/2008-322X.180699 |
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author | Ghasemi, Hassan Pourakbari, Malihe Shahidi Entezari, Morteza Yarmohammadi, Mohammad Ebrahim |
author_facet | Ghasemi, Hassan Pourakbari, Malihe Shahidi Entezari, Morteza Yarmohammadi, Mohammad Ebrahim |
author_sort | Ghasemi, Hassan |
collection | PubMed |
description | PURPOSE: To evaluate the association between age-related macular degeneration (ARMD) and sensory neural hearing impairment (SHI). METHODS: In this case-control study, hearing status of 46 consecutive patients with ARMD were compared with 46 age-matched cases without clinical ARMD as a control group. In all patients, retinal involvements were confirmed by clinical examination, fluorescein angiography (FA) and optical coherence tomography (OCT). All participants were examined with an otoscope and underwent audiological tests including pure tone audiometry (PTA), speech reception threshold (SRT), speech discrimination score (SDS), tympanometry, reflex tests and auditory brainstem response (ABR). RESULTS: A significant (P = 0.009) association was present between ARMD, especially with exudative and choroidal neovascularization (CNV) components, and age-related hearing impairment primarily involving high frequencies. Patients had higher SRT and lower SDS against anticipated presbycusis than control subjects. Similar results were detected in exudative, CNV and scar patterns supporting an association between late ARMD with SRT and SDS abnormalities. ABR showed significantly prolonged wave I and IV latency times in ARMD (P = 0.034 and 0.022, respectively). Average latency periods for wave I in geographic atrophy (GA) and CNV, and that for wave IV in drusen patterns of ARMD were significantly higher than controls (P = 0.030, 0.007 and 0.050, respectively). CONCLUSION: The association between ARMD and age-related SHI may be attributed to common anatomical components such as melanin in these two sensory organs. |
format | Online Article Text |
id | pubmed-4860988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48609882016-05-18 Association of Age Related Macular Degeneration and Age Related Hearing Impairment Ghasemi, Hassan Pourakbari, Malihe Shahidi Entezari, Morteza Yarmohammadi, Mohammad Ebrahim J Ophthalmic Vis Res Original Article PURPOSE: To evaluate the association between age-related macular degeneration (ARMD) and sensory neural hearing impairment (SHI). METHODS: In this case-control study, hearing status of 46 consecutive patients with ARMD were compared with 46 age-matched cases without clinical ARMD as a control group. In all patients, retinal involvements were confirmed by clinical examination, fluorescein angiography (FA) and optical coherence tomography (OCT). All participants were examined with an otoscope and underwent audiological tests including pure tone audiometry (PTA), speech reception threshold (SRT), speech discrimination score (SDS), tympanometry, reflex tests and auditory brainstem response (ABR). RESULTS: A significant (P = 0.009) association was present between ARMD, especially with exudative and choroidal neovascularization (CNV) components, and age-related hearing impairment primarily involving high frequencies. Patients had higher SRT and lower SDS against anticipated presbycusis than control subjects. Similar results were detected in exudative, CNV and scar patterns supporting an association between late ARMD with SRT and SDS abnormalities. ABR showed significantly prolonged wave I and IV latency times in ARMD (P = 0.034 and 0.022, respectively). Average latency periods for wave I in geographic atrophy (GA) and CNV, and that for wave IV in drusen patterns of ARMD were significantly higher than controls (P = 0.030, 0.007 and 0.050, respectively). CONCLUSION: The association between ARMD and age-related SHI may be attributed to common anatomical components such as melanin in these two sensory organs. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4860988/ /pubmed/27195086 http://dx.doi.org/10.4103/2008-322X.180699 Text en Copyright: © Journal of Ophthalmic and Vision Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Ghasemi, Hassan Pourakbari, Malihe Shahidi Entezari, Morteza Yarmohammadi, Mohammad Ebrahim Association of Age Related Macular Degeneration and Age Related Hearing Impairment |
title | Association of Age Related Macular Degeneration and Age Related Hearing Impairment |
title_full | Association of Age Related Macular Degeneration and Age Related Hearing Impairment |
title_fullStr | Association of Age Related Macular Degeneration and Age Related Hearing Impairment |
title_full_unstemmed | Association of Age Related Macular Degeneration and Age Related Hearing Impairment |
title_short | Association of Age Related Macular Degeneration and Age Related Hearing Impairment |
title_sort | association of age related macular degeneration and age related hearing impairment |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4860988/ https://www.ncbi.nlm.nih.gov/pubmed/27195086 http://dx.doi.org/10.4103/2008-322X.180699 |
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