• Neil Manwaring, Michael M Jones, Jie Jin Wang, Elena Rochtchina, Chris Howard, Phillip Newall, Paul Mitchell, and Carolyn M Sue.
• Department of Neurogenetics, Clinic 4, Royal North Shore Hospital, Reserve Road, St Leonards, New South Wales, Australia 2065.
• Arch Otolaryngol. 2007 Sep 1;133(9):929-33.

ObjectiveTo determine whether variants of the mitochondrial genome influence the risk of developing age-related hearing loss (ARHL).DesignCross-sectional study.SettingEligible participants were noninstitutionalized permanent residents 49 years or older identified in a door-to-door census of 2 suburban postcode areas, west of Sydney, Australia.ParticipantsThe Blue Mountains Hearing Study (BMHS) was a population-based survey of hearing loss, conducted during 1997 to 1999, among the participants of the Blue Mountains Eye Study cohort.Main Outcome MeasuresWe defined hearing impairment as the pure-tone average of audiometric hearing thresholds at 500, 1000, 2000, and 4000 Hz (> 25- but 40- but 60-dB HL [severe hearing loss]) in the better of the 2 ears.ResultsOf the 2765 BMHS participants, 912 (33%) were found to have ARHL. After adjusting for other hearing loss risk factors, mitochondrial DNA (mtDNA) haplogroups U and K were independently associated with a higher prevalence of ARHL compared with subjects with other haplogroups. Haplogroup U was significantly associated with moderate to severe ARHL (multivariable-adjusted odds ratio, 1.63; 95% confidence interval, 1.10-2.41). Haplogroup K was associated with severity types of ARHL in persons aged 50 to 59 years (odds ratio, 3.02; 95% confidence interval, 1.30-6.99). There was also a joint effect between mtDNA haplogroups U and K and other known hearing loss risk factors such as diabetes and past noise exposure.ConclusionFindings from this older Australian population demonstrate an association between certain mtDNA haplogroups and ARHL, as well as a link to the susceptibility of other known risk factors for ARHL.

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