Literature DB >> 35038006

AudioGene: refining the natural history of KCNQ4, GSDME, WFS1, and COCH-associated hearing loss.

Ryan K Thorpe1, W Daniel Walls1, Rae Corrigan2, Amanda Schaefer1, Kai Wang3, Patrick Huygen4, Thomas L Casavant5,6,7, Richard J H Smith8,9,10,11.   

Abstract

Autosomal dominant non-syndromic hearing loss (ADNSHL) displays gene-specific progression of hearing loss, which is amenable to sequential audioprofiling. We sought to refine the natural history of ADNSHL by examining audiometric data in 5-year increments. 2175 audiograms were included from four genetic causes of ADNSHL-KCNQ4 (DFNA2), GSDME (DFNA5), WFS1 (DFNA6/14/38), and COCH (DFNA9). Annual threshold deterioration (ATD) was calculated for each gene: for the speech-frequency pure tone average, the ATD, respectively, was 0.72 dB/year, 0.94 dB/year, 0.53 dB/year, and 1.41 dB/year, with the largest drops occurring from ages 45-50 (0.89 dB/year; KCNQ4), 5-10 (1.42 dB/year; GSDME), 40-45 (0.83 dB/year; WFS1), and 50-55 (2.09 dB/year; COCH). 5-year interval analysis of audiograms reveals the gene specific natural history of KCNQ4, GSDME, WFS1 and COCH-related progressive hearing loss. Identifying ages at which hearing loss is most rapid informs clinical care and patient expectations. Natural history data are also essential to define outcomes of clinical trials that test novel therapies designed to correct or ameliorate these genetic forms of hearing loss.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Year:  2022        PMID: 35038006      PMCID: PMC9092196          DOI: 10.1007/s00439-021-02424-7

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   5.881


  77 in total

1.  Good speech recognition and quality-of-life scores after cochlear implantation in patients with DFNA9.

Authors:  K Vermeire; J P L Brokx; F L Wuyts; E Cochet; A Hofkens; M De Bodt; P H Van de Heyning
Journal:  Otol Neurotol       Date:  2006-01       Impact factor: 2.311

2.  Genetic characteristics in children with cochlear implants and the corresponding auditory performance.

Authors:  Chen-Chi Wu; Tien-Chen Liu; Shih-Hao Wang; Chuan-Jen Hsu; Che-Ming Wu
Journal:  Laryngoscope       Date:  2011-05-06       Impact factor: 3.325

3.  Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.

Authors:  Shin-ichi Usami; Kentaro Takahashi; Isamu Yuge; Akihiro Ohtsuka; Atsushi Namba; Satoko Abe; Erik Fransen; Laszlo Patthy; Gottfried Otting; Guy Van Camp
Journal:  Eur J Hum Genet       Date:  2003-10       Impact factor: 4.246

4.  Prevalence of hearing loss and differences by demographic characteristics among US adults: data from the National Health and Nutrition Examination Survey, 1999-2004.

Authors:  Yuri Agrawal; Elizabeth A Platz; John K Niparko
Journal:  Arch Intern Med       Date:  2008-07-28

5.  AudioGene: predicting hearing loss genotypes from phenotypes to guide genetic screening.

Authors:  Kyle R Taylor; Adam P Deluca; A Eliot Shearer; Michael S Hildebrand; E Ann Black-Ziegelbein; V Nikhil Anand; Christina M Sloan; Robert W Eppsteiner; Todd E Scheetz; Patrick L M Huygen; Richard J H Smith; Terry A Braun; Thomas L Casavant
Journal:  Hum Mutat       Date:  2013-02-19       Impact factor: 4.878

6.  Histopathology of the Human Inner Ear in the p.L114P COCH Mutation (DFNA9).

Authors:  Barbara J Burgess; Jennifer T O'Malley; Takefumi Kamakura; Kris Kristiansen; Nahid G Robertson; Cynthia C Morton; Joseph B Nadol
Journal:  Audiol Neurootol       Date:  2016-03-30       Impact factor: 1.854

7.  Test-retest reliability of pure-tone thresholds from 0.5 to 16 kHz using Sennheiser HDA 200 and Etymotic Research ER-2 earphones.

Authors:  Nicolas Schmuziger; Rudolf Probst; Jacek Smurzynski
Journal:  Ear Hear       Date:  2004-04       Impact factor: 3.570

8.  Universal newborn hearing screening: a question of evidence.

Authors:  A Durieux-Smith; E Fitzpatrick; J Whittingham
Journal:  Int J Audiol       Date:  2008-01       Impact factor: 2.117

9.  WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis.

Authors:  Masafumi Kobayashi; Maiko Miyagawa; Shin-Ya Nishio; Hideaki Moteki; Taro Fujikawa; Kenji Ohyama; Hirofumi Sakaguchi; Ikuyo Miyanohara; Akiko Sugaya; Yasushi Naito; Shin-Ya Morita; Yukihiko Kanda; Masahiro Takahashi; Kotaro Ishikawa; Yuki Nagano; Tetsuya Tono; Chie Oshikawa; Chiharu Kihara; Haruo Takahashi; Yoshihiro Noguchi; Shin-Ichi Usami
Journal:  PLoS One       Date:  2018-03-12       Impact factor: 3.240

10.  Genomic Landscape and Mutational Signatures of Deafness-Associated Genes.

Authors:  Hela Azaiez; Kevin T Booth; Sean S Ephraim; Bradley Crone; Elizabeth A Black-Ziegelbein; Robert J Marini; A Eliot Shearer; Christina M Sloan-Heggen; Diana Kolbe; Thomas Casavant; Michael J Schnieders; Carla Nishimura; Terry Braun; Richard J H Smith
Journal:  Am J Hum Genet       Date:  2018-09-20       Impact factor: 11.025

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  3 in total

1.  The hearing-impaired patient: what the future holds.

Authors:  Richard J H Smith
Journal:  Hum Genet       Date:  2022-03-15       Impact factor: 5.881

Review 2.  Behavior of KCNQ Channels in Neural Plasticity and Motor Disorders.

Authors:  Som P Singh; Matthew William; Mira Malavia; Xiang-Ping Chu
Journal:  Membranes (Basel)       Date:  2022-05-06

3.  A Novel Missense WFS1 Variant: Expanding the Mutational Spectrum Associated with Nonsyndromic Low-Frequency Sensorineural Hearing Loss.

Authors:  Jingyu Ma; Rongrong Wang; Li Zhang; Shanshan Wang; Shuqing Tong; Xiaohui Bai; Zhiming Lu
Journal:  Biomed Res Int       Date:  2022-10-03       Impact factor: 3.246

  3 in total

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