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CDH23 Methylation Status and Presbycusis Risk in Elderly Women
Introduction: Presbycusis, an age-related hearing impairment (ARHI) disease, is the most common cause for HI in adults worldwide. One of the best candidate genes for ARHI susceptibility is Cadherin 23 (CDH23) which encodes stereocilia tip-links of the inner ear sensory hair cell. Although alteration...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090039/ https://www.ncbi.nlm.nih.gov/pubmed/30131691 http://dx.doi.org/10.3389/fnagi.2018.00241 |
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author | Bouzid, Amal Smeti, Ibtihel Chakroun, Amine Loukil, Salma Gibriel, Abdullah Ahmed Grati, Mhamed Ghorbel, Abdelmonem Masmoudi, Saber |
author_facet | Bouzid, Amal Smeti, Ibtihel Chakroun, Amine Loukil, Salma Gibriel, Abdullah Ahmed Grati, Mhamed Ghorbel, Abdelmonem Masmoudi, Saber |
author_sort | Bouzid, Amal |
collection | PubMed |
description | Introduction: Presbycusis, an age-related hearing impairment (ARHI) disease, is the most common cause for HI in adults worldwide. One of the best candidate genes for ARHI susceptibility is Cadherin 23 (CDH23) which encodes stereocilia tip-links of the inner ear sensory hair cell. Although alterations in the methylation status of CpG dinucleotides across various genes were reported to be associated with HI, methylation changes in CDH23 gene have not been reported previously. Objectives: This study aimed at investigating whether DNA methylation level of CDH23 gene at intragenic CpG island overlapping an exonic-intronic region at position chr10:73565570-73565827 (GRCh37/hg19) could be risk factor associated with ARHI. Materials and Methods: We screened for methylation changes in this particular position for CDH23 gene in 50 blood samples of elderly women affected with presbycusis and healthy control cohort. Methylation of CpG sites were assessed using Quantitative methylation-specific PCR (qMSP) following sodium bisulfite DNA conversion chemistry. Methylation levels were normalized against TSH2B reference gene. Results: DNA methylation analysis for the common CpG islands in CDH23 gene revealed 3.27-folds significant increase (p < 0.0001) in methylation profile for ARHI women as compared to healthy controls with an elevated risk odds ratio (OR) of 2.219 [95% CI 1.071–4.597]. Conclusion: Our study is the first of its kind to prove that higher CpG site methylation levels in CDH23 gene are likely to be associated with ARHI. |
format | Online Article Text |
id | pubmed-6090039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60900392018-08-21 CDH23 Methylation Status and Presbycusis Risk in Elderly Women Bouzid, Amal Smeti, Ibtihel Chakroun, Amine Loukil, Salma Gibriel, Abdullah Ahmed Grati, Mhamed Ghorbel, Abdelmonem Masmoudi, Saber Front Aging Neurosci Neuroscience Introduction: Presbycusis, an age-related hearing impairment (ARHI) disease, is the most common cause for HI in adults worldwide. One of the best candidate genes for ARHI susceptibility is Cadherin 23 (CDH23) which encodes stereocilia tip-links of the inner ear sensory hair cell. Although alterations in the methylation status of CpG dinucleotides across various genes were reported to be associated with HI, methylation changes in CDH23 gene have not been reported previously. Objectives: This study aimed at investigating whether DNA methylation level of CDH23 gene at intragenic CpG island overlapping an exonic-intronic region at position chr10:73565570-73565827 (GRCh37/hg19) could be risk factor associated with ARHI. Materials and Methods: We screened for methylation changes in this particular position for CDH23 gene in 50 blood samples of elderly women affected with presbycusis and healthy control cohort. Methylation of CpG sites were assessed using Quantitative methylation-specific PCR (qMSP) following sodium bisulfite DNA conversion chemistry. Methylation levels were normalized against TSH2B reference gene. Results: DNA methylation analysis for the common CpG islands in CDH23 gene revealed 3.27-folds significant increase (p < 0.0001) in methylation profile for ARHI women as compared to healthy controls with an elevated risk odds ratio (OR) of 2.219 [95% CI 1.071–4.597]. Conclusion: Our study is the first of its kind to prove that higher CpG site methylation levels in CDH23 gene are likely to be associated with ARHI. Frontiers Media S.A. 2018-08-07 /pmc/articles/PMC6090039/ /pubmed/30131691 http://dx.doi.org/10.3389/fnagi.2018.00241 Text en Copyright © 2018 Bouzid, Smeti, Chakroun, Loukil, Gibriel, Grati, Ghorbel and Masmoudi. 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) and the copyright owner(s) 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 Bouzid, Amal Smeti, Ibtihel Chakroun, Amine Loukil, Salma Gibriel, Abdullah Ahmed Grati, Mhamed Ghorbel, Abdelmonem Masmoudi, Saber CDH23 Methylation Status and Presbycusis Risk in Elderly Women |
title | CDH23 Methylation Status and Presbycusis Risk in Elderly Women |
title_full | CDH23 Methylation Status and Presbycusis Risk in Elderly Women |
title_fullStr | CDH23 Methylation Status and Presbycusis Risk in Elderly Women |
title_full_unstemmed | CDH23 Methylation Status and Presbycusis Risk in Elderly Women |
title_short | CDH23 Methylation Status and Presbycusis Risk in Elderly Women |
title_sort | cdh23 methylation status and presbycusis risk in elderly women |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090039/ https://www.ncbi.nlm.nih.gov/pubmed/30131691 http://dx.doi.org/10.3389/fnagi.2018.00241 |
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