dc.contributor.author
Haider, Haula F.
dc.contributor.author
Flook, Marisa
dc.contributor.author
Aparicio, Mariana
dc.contributor.author
Ribeiro, Diogo
dc.contributor.author
Antunes, Marilia
dc.contributor.author
Szczepek, Agnieszka J. [u.a.]
dc.date.accessioned
2018-06-08T10:27:18Z
dc.date.available
2017-11-28T11:14:38.750Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/20474
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-23777
dc.description.abstract
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.
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit
dc.title
Biomarkers of Presbycusis and Tinnitus in a Portuguese Older Population
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Front. Aging Neurosci. - 9 (2017), Artikel NRr. 346
dcterms.bibliographicCitation.doi
10.3389/fnagi.2017.00346
dcterms.bibliographicCitation.url
http://doi.org/10.3389/fnagi.2017.00346
refubium.affiliation
Charité - Universitätsmedizin Berlin
de
refubium.mycore.fudocsId
FUDOCS_document_000000028566
refubium.note.author
Der Artikel wurde in einer reinen Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000009176
dcterms.accessRights.openaire
open access