Literature DB >> 20303401

Heritability of audiometric shape parameters and familial aggregation of presbycusis in an elderly Flemish population.

Kelly Demeester1, Astrid van Wieringen, Jan-jaap Hendrickx, Vedat Topsakal, Jeroen Huyghe, Erik Fransen, Lut Van Laer, Guy Van Camp, Paul Van de Heyning.   

Abstract

This study describes the heritability of audiometric shape parameters and the familial aggregation of different types of presbycusis in a healthy, otologically screened population between 50 and 75 years old. About 342 siblings of 64 families (average family-size: 5.3) were recruited through population registries. Audiometric shape was mathematically quantified by objective parameters developed to measure size, slope, concavity, percentage of frequency-dependent and frequency-independent hearing loss and Bulge Depth. The heritability of each parameter was calculated using a variance components model. Logistic regression models were used to estimate the odds ratios (ORs). Estimates of sibling recurrence risk ratios (lambda(s)) are also provided. Heritability estimates were generally higher compared to previous studies. ORs and lambda(s) for the parameters Total Hearing Loss (size), Uniform Hearing Loss (percentage of frequency-dependent hearing loss) and Bulge Depth suggest a higher heredity for severe types of presbycusis compared to moderate or mild types. Our results suggest that the separation of the parameter 'Total Hearing Loss' into the two parameters 'Uniform Hearing Loss' and 'Non-uniform Hearing Loss' could lead to the discovery of different genetic subtypes of presbycusis. The parameter 'Bulge Depth', instead of 'Concavity', seemed to be an important parameter for classifying subjects into 'susceptible' or 'resistant' to societal or intensive environmental exposure. 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20303401     DOI: 10.1016/j.heares.2010.03.007

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  6 in total

1.  Functional analysis of candidate genes from genome-wide association studies of hearing.

Authors:  Neil J Ingham; Victoria Rook; Francesca Di Domenico; Elysia James; Morag A Lewis; Giorgia Girotto; Annalisa Buniello; Karen P Steel
Journal:  Hear Res       Date:  2020-01-02       Impact factor: 3.208

Review 2.  Translational and interdisciplinary insights into presbyacusis: A multidimensional disease.

Authors:  Mark A Eckert; Kelly C Harris; Hainan Lang; Morag A Lewis; Richard A Schmiedt; Bradley A Schulte; Karen P Steel; Kenneth I Vaden; Judy R Dubno
Journal:  Hear Res       Date:  2020-10-31       Impact factor: 3.208

Review 3.  Hearing loss and tinnitus: association studies for complex-hearing disorders in mouse and man.

Authors:  Ely Cheikh Boussaty; Rick Adam Friedman; Royce E Clifford
Journal:  Hum Genet       Date:  2021-07-27       Impact factor: 5.881

4.  Assessment of the risk factors for hearing loss in adult Nigerian population.

Authors:  Olusola Ayodele Sogebi
Journal:  Niger Med J       Date:  2013-07

Review 5.  Occupational noise exposure and hearing: a systematic review.

Authors:  Arve Lie; Marit Skogstad; Håkon A Johannessen; Tore Tynes; Ingrid Sivesind Mehlum; Karl-Christian Nordby; Bo Engdahl; Kristian Tambs
Journal:  Int Arch Occup Environ Health       Date:  2015-08-07       Impact factor: 3.015

6.  Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in Mice.

Authors:  Elisa Martelletti; Neil J Ingham; Oliver Houston; Johanna C Pass; Jing Chen; Walter Marcotti; Karen P Steel
Journal:  Front Cell Neurosci       Date:  2020-09-25       Impact factor: 5.505

  6 in total

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