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Biomarkers of Presbycusis and Tinnitus in a Portuguese Older Population
Introduction: Presbycusis or age-related hearing loss (ARHL) is a ubiquitous health problem. It is estimated that it will affect up to 1.5 billion people by 2025. In addition, tinnitus occurs in a large majority of cases with presbycusis. Glutamate metabotropic receptor 7 (GRM7) and N-acetyltransfer...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5672025/ https://www.ncbi.nlm.nih.gov/pubmed/29163129 http://dx.doi.org/10.3389/fnagi.2017.00346 |
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author | Haider, Haúla F. Flook, Marisa Aparicio, Mariana Ribeiro, Diogo Antunes, Marilia Szczepek, Agnieszka J. Hoare, Derek J. Fialho, Graça Paço, João C. Caria, Helena |
author_facet | Haider, Haúla F. Flook, Marisa Aparicio, Mariana Ribeiro, Diogo Antunes, Marilia Szczepek, Agnieszka J. Hoare, Derek J. Fialho, Graça Paço, João C. Caria, Helena |
author_sort | Haider, Haúla F. |
collection | PubMed |
description | Introduction: Presbycusis or age-related hearing loss (ARHL) is a ubiquitous health problem. It is estimated that it will affect up to 1.5 billion people by 2025. In addition, tinnitus occurs in a large majority of cases with presbycusis. Glutamate metabotropic receptor 7 (GRM7) and N-acetyltransferase 2 (NAT2) are some of the genetic markers for presbycusis. Objectives: To explore patterns of hearing loss and the role of GRM7 and NAT2 as possible markers of presbycusis and tinnitus in a Portuguese population sample. Materials and Methods: Tonal and speech audiometry, tinnitus assessment, clinical interview, and DNA samples were obtained from patients aged from 55 to 75 with or without tinnitus. GRM7 analysis was performed by qPCR. Genotyping of single nucleotide polymorphisms (SNPs) in NAT2 was performed by PCR amplification followed by Sanger sequencing or by qPCR. Results: We screened samples from 78 individuals (33 men and 45 women). T allele at GRM7 gene was the most observed (60.3% T/T and 33.3% A/T). Individuals with a T/T genotype have a higher risk for ARHL and 33% lower risk for tinnitus, compared to individuals with A/A and A/T genotype, respectively. Being a slow acetylator (53%) was the most common NAT2 phenotype, more common in men (55.8%). Intermediate acetylator was the second most common phenotype (35.9%) also more frequent in men (82.6%). Noise exposed individuals and individuals with ‘high frequency’ hearing loss seem to have a higher risk for tinnitus. Our data suggests that allele AT of GRM7 can have a statistically significant influence toward the severity of tinnitus. Conclusion: For each increasing year of age the chance of HL increases by 9%. The risk for ARHL was not significantly associated with GRM7 neither NAT2. However, we cannot conclude from our data whether the presence of T allele at GRM7 increases the odds for ARHL or whether the A allele has a protective effect. Genotype A/T at GRM7 could potentially be considered a biomarker of tinnitus severity. This is the first study evaluating the effect of GRM7 and NAT2 gene in tinnitus. |
format | Online Article Text |
id | pubmed-5672025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56720252017-11-21 Biomarkers of Presbycusis and Tinnitus in a Portuguese Older Population Haider, Haúla F. Flook, Marisa Aparicio, Mariana Ribeiro, Diogo Antunes, Marilia Szczepek, Agnieszka J. Hoare, Derek J. Fialho, Graça Paço, João C. Caria, Helena Front Aging Neurosci Neuroscience Introduction: Presbycusis or age-related hearing loss (ARHL) is a ubiquitous health problem. It is estimated that it will affect up to 1.5 billion people by 2025. In addition, tinnitus occurs in a large majority of cases with presbycusis. Glutamate metabotropic receptor 7 (GRM7) and N-acetyltransferase 2 (NAT2) are some of the genetic markers for presbycusis. Objectives: To explore patterns of hearing loss and the role of GRM7 and NAT2 as possible markers of presbycusis and tinnitus in a Portuguese population sample. Materials and Methods: Tonal and speech audiometry, tinnitus assessment, clinical interview, and DNA samples were obtained from patients aged from 55 to 75 with or without tinnitus. GRM7 analysis was performed by qPCR. Genotyping of single nucleotide polymorphisms (SNPs) in NAT2 was performed by PCR amplification followed by Sanger sequencing or by qPCR. Results: We screened samples from 78 individuals (33 men and 45 women). T allele at GRM7 gene was the most observed (60.3% T/T and 33.3% A/T). Individuals with a T/T genotype have a higher risk for ARHL and 33% lower risk for tinnitus, compared to individuals with A/A and A/T genotype, respectively. Being a slow acetylator (53%) was the most common NAT2 phenotype, more common in men (55.8%). Intermediate acetylator was the second most common phenotype (35.9%) also more frequent in men (82.6%). Noise exposed individuals and individuals with ‘high frequency’ hearing loss seem to have a higher risk for tinnitus. Our data suggests that allele AT of GRM7 can have a statistically significant influence toward the severity of tinnitus. Conclusion: For each increasing year of age the chance of HL increases by 9%. The risk for ARHL was not significantly associated with GRM7 neither NAT2. However, we cannot conclude from our data whether the presence of T allele at GRM7 increases the odds for ARHL or whether the A allele has a protective effect. Genotype A/T at GRM7 could potentially be considered a biomarker of tinnitus severity. This is the first study evaluating the effect of GRM7 and NAT2 gene in tinnitus. Frontiers Media S.A. 2017-11-01 /pmc/articles/PMC5672025/ /pubmed/29163129 http://dx.doi.org/10.3389/fnagi.2017.00346 Text en Copyright © 2017 Haider, Flook, Aparicio, Ribeiro, Antunes, Szczepek, Hoare, Fialho, Paço and Caria. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Haider, Haúla F. Flook, Marisa Aparicio, Mariana Ribeiro, Diogo Antunes, Marilia Szczepek, Agnieszka J. Hoare, Derek J. Fialho, Graça Paço, João C. Caria, Helena Biomarkers of Presbycusis and Tinnitus in a Portuguese Older Population |
title | Biomarkers of Presbycusis and Tinnitus in a Portuguese Older Population |
title_full | Biomarkers of Presbycusis and Tinnitus in a Portuguese Older Population |
title_fullStr | Biomarkers of Presbycusis and Tinnitus in a Portuguese Older Population |
title_full_unstemmed | Biomarkers of Presbycusis and Tinnitus in a Portuguese Older Population |
title_short | Biomarkers of Presbycusis and Tinnitus in a Portuguese Older Population |
title_sort | biomarkers of presbycusis and tinnitus in a portuguese older population |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5672025/ https://www.ncbi.nlm.nih.gov/pubmed/29163129 http://dx.doi.org/10.3389/fnagi.2017.00346 |
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