2009
DOI: 10.1002/lary.20218
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Quantification of the mitochondrial DNA common deletion in presbycusis

Abstract: For the first time, to our knowledge, these results demonstrate a relationship between quantitatively measured levels of the CD in human cochlear tissue and the severity of hearing loss in individuals with presbycusis. Laryngoscope, 2009.

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Cited by 87 publications
(63 citation statements)
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References 19 publications
(28 reference statements)
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“…Recently, real-time PCR has been developed to investigate either mtDNA copy number or the percentage of common deletion in every subject [23] . A recent study which used real-time PCR to quantify the percentage of common deletion in archival temporal bone reported that presbycusis group had a mean common deletion level of 32% in archival temporal bone and normal hearing control group had only 12% in archival temporal bone [24] . Although the available evidence indicates that the common deletion is related to presbycusis, the specific role of this deletion in the generation of presbycusis remains unclear.…”
Section: Discussionmentioning
confidence: 99%
“…Recently, real-time PCR has been developed to investigate either mtDNA copy number or the percentage of common deletion in every subject [23] . A recent study which used real-time PCR to quantify the percentage of common deletion in archival temporal bone reported that presbycusis group had a mean common deletion level of 32% in archival temporal bone and normal hearing control group had only 12% in archival temporal bone [24] . Although the available evidence indicates that the common deletion is related to presbycusis, the specific role of this deletion in the generation of presbycusis remains unclear.…”
Section: Discussionmentioning
confidence: 99%
“…As compared with previous in vivo studies (3,15,26), analyzing mtDNA expression in peripheral blood and temporal bone specimens, the present study was non-invasive and effective through analysis of mtDNA CD4977 in the hair shaft. Therefore, hair shaft detection may be used to predict hearing function.…”
mentioning
confidence: 86%
“…Presbycusis is characterized by the progressive, bilaterally symmetrical, sensorineural and chronic loss of hearing. Although the mechanism of presbycusis is unclear, Markaryan A et al (3) demonstrated histopathologically, that degeneration of cochlea tissues, including the spiral ganglion, stria vascularis and hair cells, was linearly associated with hearing loss (3).…”
Section: Introductionmentioning
confidence: 99%
“…These observations were confi rmed in humans by Dai et al ( 2004 ), who found a high incidence of the mtDNA4977 deletion in the temporal bones of ARHL patients (17/34) compared to ears in the age-matched control group (4/19) and those in the young and middleaged control group (0/14). Perhaps most compelling, a quantitative correlation was established between the level of the mtDNA4977 deletion in human temporal bone samples from ARHL patients and the severity of the hearing loss (Markaryan et al 2009 ). These authors also observed a decrease in the expression of the mitochondrial cytochrome c oxidase subunit 3 (COX3) gene in SGNs and an increase in deletions different from the mtDNA common deletion in COX3-defi cient SGNs (Markaryan et al 2010 ).…”
Section: Mitochondrial Mutations and Dysfunction And Its Association mentioning
confidence: 99%