Literature DB >> 18776599

Susceptibility genes for gentamicin-induced vestibular dysfunction.

Stephen M Roth1, Scott M Williams, Lan Jiang, Kalapurakkal S Menon, John J Jeka.   

Abstract

BACKGROUND: Approximately 5% of patients administered gentamicin (GM), an aminoglycoside antibiotic, experience vestibular ototoxicity resulting in balance dysfunction. In the present study, we sought to identify susceptibility genes associated with GM-induced vestibular dysfunction using a case/control design.
METHODS: White cases (n=137; 55 men, 82 women) were recruited based on physician-confirmed unilateral or bilateral vestibular dysfunction attributed to GM administration. Controls (n=126; 54 men, 72 women) were healthy, age-matched individuals without vestibular dysfunction or balance impairment. Buccal cell samples were obtained from all subjects and DNA was genotyped for 15 polymorphisms in 9 genes. Candidate genes were identified primarily for their roles in oxidative stress based on predicted mechanisms of gentamicin-induced ototoxicity. Statistical analyses included the multi-dimensionality reduction (MDR) method for identifying gene x gene interactions across multiple candidate genes.
RESULTS: Both single gene and MDR analyses revealed the NOS3 (ENOS) p.Glu298Asp polymorphism as significantly associated with GM-induced vestibular dysfunction (both p <or= 0.03). MDR analysis revealed a three-gene combination, consisting of NOS3 (p.Glu298Asp), GSTZ1 (p.Lys32Glu), and GSTP1 (p.Ile105Val), that provided the highest predictive model for GM-induced vestibular dysfunction (64% accuracy; p=0.009).
CONCLUSIONS: The results indicate that carriers of risk alleles at three oxidative stress-related genes have increased susceptibility to GM-induced vestibular dysfunction.

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Year:  2008        PMID: 18776599      PMCID: PMC2581796     

Source DB:  PubMed          Journal:  J Vestib Res        ISSN: 0957-4271            Impact factor:   2.435


  41 in total

1.  Maturation of cochlear glutathione-S-transferases correlates with the end of the sensitive period for ototoxicity.

Authors:  D S Whitlon; L S Wright; S A Nelson; R Szakaly; F L Siegel
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2.  Ototoxicity caused by aminoglycosides.

Authors:  Maria Bitner-Glindzicz; Shamima Rahman
Journal:  BMJ       Date:  2007-10-20

3.  Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer.

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Journal:  Am J Hum Genet       Date:  2001-06-11       Impact factor: 11.025

Review 4.  Glutathione S-transferase polymorphisms and their biological consequences.

Authors:  J D Hayes; R C Strange
Journal:  Pharmacology       Date:  2000-09       Impact factor: 2.547

Review 5.  Neurotrophins, NMDA receptors, and nitric oxide in development and protection of the auditory system.

Authors:  K Agerman; B Canlon; M Duan; P Ernfors
Journal:  Ann N Y Acad Sci       Date:  1999-11-28       Impact factor: 5.691

Review 6.  Genetic factors in aminoglycoside toxicity.

Authors:  N Fischel-Ghodsian
Journal:  Ann N Y Acad Sci       Date:  1999-11-28       Impact factor: 5.691

Review 7.  Antioxidant therapy attenuates aminoglycoside-induced hearing loss.

Authors:  J Schacht
Journal:  Ann N Y Acad Sci       Date:  1999-11-28       Impact factor: 5.691

8.  Nitric oxide synthase inhibitor reduces the apoptotic change in the cisplatin-treated cochlea of guinea pigs.

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Review 9.  DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15.

Authors:  T B Friedman; J T Hinnant; R A Fridell; E R Wilcox; Y Raphael; S A Camper
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10.  MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.

Authors:  S Melchionda; N Ahituv; L Bisceglia; T Sobe; F Glaser; R Rabionet; M L Arbones; A Notarangelo; E Di Iorio; M Carella; L Zelante; X Estivill; K B Avraham; P Gasparini
Journal:  Am J Hum Genet       Date:  2001-07-20       Impact factor: 11.025

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2.  [Current aspects of ototoxicity. Ototoxic substances and their effects].

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3.  Novel deleterious mutation in MYO7A, TH and EVC2 in two Pakistani brothers with familial deafness.

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Review 4.  Genetic Factors of Nitric Oxide's System in Psychoneurologic Disorders.

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Review 5.  Bilateral Vestibular Weakness.

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