Literature DB >> 17909436

The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss.

Els Van Eyken1, Lut Van Laer, Erik Fransen, Vedat Topsakal, Jan-Jaap Hendrickx, Kelly Demeester, Paul Van de Heyning, Elina Mäki-Torkko, Samuli Hannula, Martti Sorri, Mona Jensen, Agnete Parving, Michael Bille, Manuela Baur, Markus Pfister, Amanda Bonaconsa, Manuela Mazzoli, Eva Orzan, Angeles Espeso, Dafydd Stephens, Katia Verbruggen, Joke Huyghe, Ingeborg Dhooge, Patrick Huygen, Hannie Kremer, Cor Cremers, Sylvia Kunst, Mina Manninen, Ilmari Pyykkö, Elzbieta Rajkowska, Malgorzata Pawelczyk, Mariola Sliwinska-Kowalska, Michael Steffens, Thomas Wienker, Guy Van Camp.   

Abstract

HYPOTHESIS: The common GJB2 (Connexin 26) 35delG mutation might contribute to the development of age-related hearing impairment (ARHI) and noise-induced hearing loss (NIHL).
BACKGROUND: GJB2, a gene encoding a gap junction protein expressed in the inner ear, has been suggested to be involved in the potassium recycling pathway in the cochlea. GJB2 mutations account for a large number of individuals with nonsyndromic recessive hearing loss, with 35delG being the most frequent mutation in populations of European origin. Other genes involved in potassium homeostasis have been suggested to be associated with ARHI and NIHL, and distortion product otoacoustic emission distortions indicative of hearing loss alterations have been found in 35delG carriers.
METHOD: We genotyped 35delG in two distinct sample sets: an ARHI sample set, composed of 2,311 Caucasian samples from nine different centers originating from seven different countries with an age range between 53 and 67 years, and an NIHL sample set consisting of 702 samples from the two extremes of a noise-exposed Polish sample.
RESULTS: After statistical analysis, we were unable to detect an association between 35delG and ARHI, nor between 35delG and NIHL.
CONCLUSION: Our findings indicate that there is no increased susceptibility in 35delG carriers for the development of ARHI or NIHL.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17909436     DOI: 10.197/MAO.0b013e3180dca1b9

Source DB:  PubMed          Journal:  Otol Neurotol        ISSN: 1531-7129            Impact factor:   2.311


  17 in total

1.  Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.

Authors:  Zubair M Ahmed; Rizwan Yousaf; Byung Cheon Lee; Shaheen N Khan; Sue Lee; Kwanghyuk Lee; Tayyab Husnain; Atteeq Ur Rehman; Sarah Bonneux; Muhammad Ansar; Wasim Ahmad; Suzanne M Leal; Vadim N Gladyshev; Inna A Belyantseva; Guy Van Camp; Sheikh Riazuddin; Thomas B Friedman; Saima Riazuddin
Journal:  Am J Hum Genet       Date:  2010-12-23       Impact factor: 11.025

2.  GRM7 variants confer susceptibility to age-related hearing impairment.

Authors:  Rick A Friedman; Lut Van Laer; Matthew J Huentelman; Sonal S Sheth; Els Van Eyken; Jason J Corneveaux; Waibhav D Tembe; Rebecca F Halperin; Ashley Q Thorburn; Sofie Thys; Sarah Bonneux; Erik Fransen; Jeroen Huyghe; Ilmari Pyykkö; Cor W R J Cremers; Hannie Kremer; Ingeborg Dhooge; Dafydd Stephens; Eva Orzan; Markus Pfister; Michael Bille; Agnete Parving; Martti Sorri; Paul H Van de Heyning; Linna Makmura; Jeffrey D Ohmen; Frederick H Linthicum; Jose N Fayad; John V Pearson; David W Craig; Dietrich A Stephan; Guy Van Camp
Journal:  Hum Mol Genet       Date:  2008-12-01       Impact factor: 6.150

Review 3.  Inner ear drug delivery for auditory applications.

Authors:  Erin E Leary Swan; Mark J Mescher; William F Sewell; Sarah L Tao; Jeffrey T Borenstein
Journal:  Adv Drug Deliv Rev       Date:  2008-09-21       Impact factor: 15.470

4.  Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss.

Authors:  Christopher Beck; Jose Carmelo Pérez-Álvarez; Alexander Sigruener; Frank Haubner; Till Seidler; Charalampos Aslanidis; Jürgen Strutz; Gerd Schmitz
Journal:  Eur Arch Otorhinolaryngol       Date:  2014-09-12       Impact factor: 2.503

Review 5.  Sex-based Differences in Hearing Loss: Perspectives From Non-clinical Research to Clinical Outcomess.

Authors:  Dillan F Villavisanis; Elisa R Berson; Amanda M Lauer; Maura K Cosetti; Katrina M Schrode
Journal:  Otol Neurotol       Date:  2020-03       Impact factor: 2.311

6.  FVB/NJ mice demonstrate a youthful sensitivity to noise-induced hearing loss and provide a useful genetic model for the study of neural hearing loss.

Authors:  Maria K Ho; Xin Li; Juemei Wang; Jeffrey D Ohmen; Rick A Friedman
Journal:  Audiol Neurotol Extra       Date:  2014-01-01

Review 7.  Noise-Induced Hearing Loss: Updates on Molecular Targets and Potential Interventions.

Authors:  Huanyu Mao; Yan Chen
Journal:  Neural Plast       Date:  2021-07-06       Impact factor: 3.599

8.  Prevalence and audiological features in carriers of GJB2 mutations, c.35delG and c.101T>C (p.M34T), in a UK population study.

Authors:  Amanda Hall; Marcus Pembrey; Mark Lutman; Colin Steer; Maria Bitner-Glindzicz
Journal:  BMJ Open       Date:  2012-07-31       Impact factor: 2.692

9.  Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairment.

Authors:  Chen-Chi Wu; Yin-Hung Lin; Ying-Chang Lu; Pei-Jer Chen; Wei-Shiung Yang; Chuan-Jen Hsu; Pei-Lung Chen
Journal:  PLoS One       Date:  2013-02-22       Impact factor: 3.240

10.  Noise stresses the junctions to deaf.

Authors:  Karen B Avraham
Journal:  EMBO Mol Med       Date:  2009-05       Impact factor: 12.137

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.