Literature DB >> 27859305

Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4.

Jane Rose1, Julie A Muskett1, Kelly A King1, Christopher K Zalewski1, Parna Chattaraj1, John A Butman2, Margaret A Kenna3,4, Wade W Chien5, Carmen C Brewer1, Andrew J Griffith1.   

Abstract

OBJECTIVES/HYPOTHESIS: To characterize the severity and natural history of hearing loss, and the prevalence of having a cochlear implant in a maturing cohort of individuals with enlarged vestibular aqueduct (EVA) and zero or one mutant allele of SLC26A4. STUDY
DESIGN: Prospective cohort study of subjects ascertained between 1998 and 2015 at the National Institutes of Health Clinical Center.
METHODS: Study subjects were 127 individuals (median age, 8 years; range, 0-59 years) with EVA in at least one ear.
RESULTS: Ears with EVA and zero or one mutant allele of SLC26A4 had mean 0.5/1/2/4-kHz pure-tone averages of 62.6 and 52.9 dB HL, respectively, in contrast to EVA ears with two mutant alleles of SLC26A4 (88.1 dB HL; P < .01). This association was independent of age, sex, or side of EVA (P < .001). Natural history of hearing loss was not associated with number of mutant alleles (P = .94). The prevalence of having a cochlear implant was nine (12%) of 76, two (13%) of 15, and 12 (38%) of 32 subjects with zero, one, and two mutant alleles, respectively (P = .00833). This association was not independent (P = .534) but reflected underlying correlations with age at time of first audiogram (P = .003) or severity of hearing loss (P = .000).
CONCLUSIONS: Ears with EVA and zero or one mutant allele of SLC26A4 have less severe hearing loss, no difference in prevalence of fluctuation, and a lower prevalence of cochlear implantation in comparison to ears with two mutant alleles of SLC26A4. LEVEL OF EVIDENCE: NA Laryngoscope, 127:E238-E243, 2017.
© 2016 The American Laryngological, Rhinological and Otological Society, Inc.

Entities:  

Keywords:  Cochlear implant; Pendred syndrome; SLC26A4; congenital anomalies; fluctuation; hearing loss; natural history; non-syndromic; otology; pediatric otology; progression

Mesh:

Substances:

Year:  2016        PMID: 27859305      PMCID: PMC6224160          DOI: 10.1002/lary.26418

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  12 in total

1.  Atypical patterns of segregation of familial enlargement of the vestibular aqueduct.

Authors:  Julie A Muskett; Parna Chattaraj; John F Heneghan; Fabian R Reimold; Boris E Shmukler; Carmen C Brewer; Kelly A King; Christopher K Zalewski; Thomas H Shawker; John A Butman; Margaret A Kenna; Wade W Chien; Seth L Alper; Andrew J Griffith
Journal:  Laryngoscope       Date:  2015-10-20       Impact factor: 3.325

2.  Genetic basis of hearing loss associated with enlarged vestibular aqueducts in Koreans.

Authors:  H-J Park; S-J Lee; H-S Jin; J O Lee; S-H Go; H S Jang; S-K Moon; S-C Lee; Y-M Chun; H-K Lee; J-Y Choi; S-C Jung; A J Griffith; S K Koo
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3.  SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.

Authors:  Sébastien Albert; Hélène Blons; Laurence Jonard; Delphine Feldmann; Pierre Chauvin; Nathalie Loundon; Annie Sergent-Allaoui; Muriel Houang; Alain Joannard; Sébastien Schmerber; Bruno Delobel; Jacques Leman; Hubert Journel; Hélène Catros; Hélène Dollfus; Marie-Madeleine Eliot; Albert David; Catherine Calais; Valérie Drouin-Garraud; Marie-Françoise Obstoy; Patrice Tran Ba Huy; Didier Lacombe; Françoise Duriez; Christine Francannet; Pierre Bitoun; Christine Petit; Eréa-Noël Garabédian; Rémy Couderc; Sandrine Marlin; Françoise Denoyelle
Journal:  Eur J Hum Genet       Date:  2006-06       Impact factor: 4.246

4.  A new standardized format for reporting hearing outcome in clinical trials.

Authors:  Richard K Gurgel; Robert K Jackler; Robert A Dobie; Gerald R Popelka
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5.  Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueduct.

Authors:  Parna Chattaraj; Fabian R Reimold; Julie A Muskett; Boris E Shmukler; Wade W Chien; Anne C Madeo; Shannon P Pryor; Christopher K Zalewski; John A Butman; Carmen C Brewer; Margaret A Kenna; Seth L Alper; Andrew J Griffith
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6.  SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities.

Authors:  S P Pryor; A C Madeo; J C Reynolds; N J Sarlis; K S Arnos; W E Nance; Y Yang; C K Zalewski; C C Brewer; J A Butman; A J Griffith
Journal:  J Med Genet       Date:  2005-02       Impact factor: 6.318

7.  Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes.

Authors:  B Y Choi; A C Madeo; K A King; C K Zalewski; S P Pryor; J A Muskett; W E Nance; J A Butman; C C Brewer; A J Griffith
Journal:  J Med Genet       Date:  2009-07-02       Impact factor: 6.318

8.  Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?

Authors:  Byung Yoon Choi; Andrew K Stewart; Anne C Madeo; Shannon P Pryor; Suzanne Lenhard; Rick Kittles; David Eisenman; H Jeffrey Kim; John Niparko; James Thomsen; Kathleen S Arnos; Walter E Nance; Kelly A King; Christopher K Zalewski; Carmen C Brewer; Thomas Shawker; James C Reynolds; John A Butman; Lawrence P Karniski; Seth L Alper; Andrew J Griffith
Journal:  Hum Mutat       Date:  2009-04       Impact factor: 4.878

9.  Genotype-phenotype correlations for SLC26A4-related deafness.

Authors:  Hela Azaiez; Tao Yang; Sai Prasad; Jessica L Sorensen; Carla J Nishimura; William J Kimberling; Richard J H Smith
Journal:  Hum Genet       Date:  2007-08-10       Impact factor: 4.132

10.  The large vestibular aqueduct: a new definition based on audiologic and computed tomography correlation.

Authors:  Mark Boston; Mark Halsted; Jareen Meinzen-Derr; Judy Bean; Shyan Vijayasekaran; Ellis Arjmand; Daniel Choo; Corning Benton; John Greinwald
Journal:  Otolaryngol Head Neck Surg       Date:  2007-06       Impact factor: 3.497

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  6 in total

1.  A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct.

Authors:  Parna Chattaraj; Tina Munjal; Keiji Honda; Nanna D Rendtorff; Jessica S Ratay; Julie A Muskett; Davide S Risso; Isabelle Roux; E Michael Gertz; Alejandro A Schäffer; Thomas B Friedman; Robert J Morell; Lisbeth Tranebjærg; Andrew J Griffith
Journal:  J Med Genet       Date:  2017-08-05       Impact factor: 6.318

2.  Compendium of causative genes and their encoded proteins for common monogenic disorders.

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3.  Functional Testing of SLC26A4 Variants-Clinical and Molecular Analysis of a Cohort with Enlarged Vestibular Aqueduct from Austria.

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Journal:  Int J Mol Sci       Date:  2018-01-10       Impact factor: 5.923

4.  SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct.

Authors:  Janet R Chao; Parna Chattaraj; Tina Munjal; Keiji Honda; Kelly A King; Christopher K Zalewski; Wade W Chien; Carmen C Brewer; Andrew J Griffith
Journal:  BMC Med Genet       Date:  2019-07-02       Impact factor: 2.103

Review 5.  Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss.

Authors:  Keiji Honda; Andrew J Griffith
Journal:  Hum Genet       Date:  2021-08-03       Impact factor: 4.132

6.  Enlarged vestibular aqueduct and Mondini Malformation: audiological, clinical, radiologic and genetic features.

Authors:  F Forli; F Lazzerini; G Auletta; L Bruschini; S Berrettini
Journal:  Eur Arch Otorhinolaryngol       Date:  2020-09-10       Impact factor: 2.503

  6 in total

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