Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment.

TitleMitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment.
Publication TypeJournal Article
Year of Publication2005
AuthorsJacobs, HT, Hutchin, TP, Käppi, T, Gillies, G, Minkkinen, K, Walker, J, Thompson, K, Rovio, AT, Carella, M, Melchionda, S, Zelante, L, Gasparini, P, Pyykkö, I, Shah, ZH, Zeviani, M, Mueller, RF
JournalEur J Hum Genet
Volume13
Issue1
Pagination26-33
Date Published2005 Jan
ISSN1018-4813
KeywordsAge of Onset, Aged, Aged, 80 and over, DNA Mutational Analysis, DNA, Mitochondrial, Female, Finland, Haplotypes, Hearing Loss, Humans, Italy, Language Disorders, Male, Middle Aged, Mutation, Polymorphism, Single Nucleotide, United Kingdom
Abstract

Mitochondrial mutations have previously been reported anecdotally in families with maternally inherited, nonsyndromic hearing impairment. To ascertain the contribution of mitochondrial mutations to postlingual but early-onset, nonsyndromic hearing impairment, we screened patients collected from within two different populations (southern Italy and UK) for previously reported mtDNA mutations associated with hearing disorders. Primer extension (SNP analysis) was used to screen for specific mutations, revealing cases of heteroplasmy and its extent. The most frequently implicated tRNA genes, Leu(UUR) and Ser(UCN), were also sequenced in all Italian patients. All tRNA genes were sequenced in those UK patients showing the clearest likelihood of maternal inheritance. Causative mtDNA mutations were found in approximately 5% of patients in both populations, representing almost 10% of cases that were clearly familial. Age of onset, where known, was generally before adulthood, and hearing loss was typically progressive. Haplogroup analysis revealed a possible excess of haplogroup cluster HV in the patients, compared with population controls, but of borderline statistical significance. In contrast, we did not find any of the previously reported mtDNA mutations, nor a significant deviation from haplogroup cluster frequencies typical of the control population, in patients with late adult-onset hearing loss (age-related hearing impairment) from the UK or Finland.

DOI10.1038/sj.ejhg.5201250
Alternate JournalEur. J. Hum. Genet.
Citation Key10.1038/sj.ejhg.5201250
PubMed ID15292920
Grant ListGGP030039 / / Telethon / Italy