Abstract | CONTEXT:
Presbycusis, an age-related hearing impairment (ARHI), represents the most common sensory disability in adults. Today, the molecular mechanisms underlying presbycusis remain unclear. This is in particular due to the fact that ARHI is a multifactorial complex disorder resulting from several genomic factors interacting with lifelong cumulative effects of: disease, diet, and environment. OBJECTIVE: MATERIALS AND METHODS: We selectively ascertained 18 elderly unrelated women lacking environmental and metabolic risk factors. Subsequently, we screened for methylation map changes in blood samples of women with presbycusis as compared to controls, using reduced representation bisulfite sequencing. We focused on hypermethylated cytosine bases located in gene promoters and the first two exons. To elucidate the related gene expression changes, we performed transcriptomic study using gene expression microarray. RESULTS: Twenty-seven genes, known to be expressed in adult human cochlea, were found in the blood cells to be differentially hypermethylated with significant (p < 0.01) methylation differences (>30%) and down-expressed with fold change >1.2 (FDR <0.05). Functional annotation and qRT-PCR further identified P2RX2, KCNQ5, ERBB3 and SOCS3 to be associated with the progression of ARHI. DISCUSSION AND CONCLUSION: Down-expressed genes associated with DNA hypermethylation could be used as biomarkers for understanding complex pathogenic mechanisms underlying presbycusis.
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Authors | Amal Bouzid, Ibtihel Smeti, Leila Dhouib, Magali Roche, Imen Achour, Aida Khalfallah, Abdullah Ahmed Gibriel, Ilhem Charfeddine, Hammadi Ayadi, Joel Lachuer, Abdelmonem Ghorbel, Christine Petit, Saber Masmoudi |
Journal | Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals
(Biomarkers)
2018 May - Jun
Vol. 23
Issue 4
Pg. 347-356
ISSN: 1366-5804 [Electronic] England |
PMID | 29325454
(Publication Type: Journal Article)
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Chemical References |
- KCNQ Potassium Channels
- KCNQ5 protein, human
- P2RX2 protein, human
- Receptors, Purinergic P2X2
- SOCS3 protein, human
- Suppressor of Cytokine Signaling 3 Protein
- ERBB3 protein, human
- Receptor, ErbB-3
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Topics |
- Aged
- Aged, 80 and over
- Case-Control Studies
- DNA Methylation
(physiology)
- Down-Regulation
- Female
- Humans
- KCNQ Potassium Channels
(genetics)
- Microarray Analysis
- Presbycusis
(genetics)
- Receptor, ErbB-3
(genetics)
- Receptors, Purinergic P2X2
(genetics)
- Suppressor of Cytokine Signaling 3 Protein
(genetics)
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