𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Quantification of the mitochondrial DNA common deletion in presbycusis

✍ Scribed by Adam Markaryan; Erik G. Nelson; Raul Hinojosa


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
628 KB
Volume
119
Category
Article
ISSN
0023-852X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Objectives/Hypothesis:

This study was conducted to evaluate the association between the mitochondrial DNA (mtDNA) common deletion (CD) level in cochlear tissue and the severity of hearing loss in individuals with presbycusis.

Study Design:

Nineteen individuals with presbycusis, ranging from 60 to 87 years of age, who met strict audiometric criteria were compared with four age frequency‐matched normal hearing controls ranging from 51 to 76 years of age. Five additional normal hearing individuals, ranging from 9 to 50 years of age, were also studied.

Methods:

A duplex real time polymerase chain reaction assay was used to quantify the mtDNA in archival cochlear tissue samples. Linear regression models were used for comparison of the CD level between groups.

Results:

The presbycusis group had a mean CD level of 32% with a standard deviation of 14%, and the normal hearing age matched control group had a mean CD level of 12% with a standard deviation of 2%. This difference in CD levels reached statistical significance (P = .011) and remained significant after adjusting for any differences in age between the two groups (age‐adjusted P = .007). Furthermore, there was evidence for a significant association between the CD level and the severity of hearing loss based on audiometric thresholds at 8 kHz (r = 0.44, P = .034; age‐adjusted partial correlation = 0.55, P = .007).

Conclusions:

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


📜 SIMILAR VOLUMES


Tissue distribution and transmission of
✍ M. Zeviani; C. Gallera; M. Pannacci; G. Uziel; A. Prelle; S. Servidei; Dr S. DiD 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 468 KB 👁 2 views

## Abstract By using a combination of Southern blot hybridization analysis, polymerase–chain reaction amplification, and direct nucleotide sequencing, we studied deletions of mitochondrial DNA (mtDNA) in several nonfamilial patients with progressive external ophthalmoplegia and Kearns‐Sayre syndrom

Method for in situ investigation of mito
✍ Sergey A. Kovalenko; Paul J. Harms; Masashi Tanaka; Alessandra Baumer; Joanne Ke 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 317 KB 👁 2 views

A number of mitochondrial DNA (mtDNA) deletions have been recently identified in the tissues of patients with mitochondrial diseases and in elderly individuals. To investigate the distribution of mutant mitochondrial genomes within any particular tissue, we have developed a sensitive method based on

Analysis of multiple mitochondrial DNA d
✍ Ali-Reza Moslemi; Christopher Lindberg; Anders Oldfors 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 238 KB 👁 2 views

Inclusion body myositis (IBM) is a sporadic progressive myopathy, which is morphologically characterized by inflammatory cell infiltrates and rimmed vacuoles in muscle fibers. Mitochondrial changes are regularly present with ragged-red fibers showing deficiency of cytochrome c oxidase. In these musc