Till Örebro universitet

oru.seÖrebro universitets publikationer
Ändra sökning
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss
Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Department of Otorhinolaryngology, University Hospital of Antwerp, Antwerp, Belgium.
Visa övriga samt affilieringar
2007 (Engelska)Ingår i: Otology and Neurotology, ISSN 1531-7129, E-ISSN 1537-4505, Vol. 28, nr 7, s. 970-975Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

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.

Ort, förlag, år, upplaga, sidor
2007. Vol. 28, nr 7, s. 970-975
Nationell ämneskategori
Oto-rino-laryngologi Medicinsk genetik och genomik
Identifikatorer
URN: urn:nbn:se:oru:diva-63474ISI: 000249858400019PubMedID: 17909436OAI: oai:DiVA.org:oru-63474DiVA, id: diva2:1168026
Tillgänglig från: 2017-12-19 Skapad: 2017-12-19 Senast uppdaterad: 2025-02-10Bibliografiskt granskad

Open Access i DiVA

Fulltext saknas i DiVA

Övriga länkar

PubMedAbstract

Person

Mäki-Torkko, Elina

Sök vidare i DiVA

Av författaren/redaktören
Mäki-Torkko, Elina
Av organisationen
Institutionen för medicinska vetenskaper
I samma tidskrift
Otology and Neurotology
Oto-rino-laryngologiMedicinsk genetik och genomik

Sök vidare utanför DiVA

GoogleGoogle Scholar

pubmed
urn-nbn

Altmetricpoäng

pubmed
urn-nbn
Totalt: 397 träffar
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf