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Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 Genotype.
McDermott, John Henry; Wolf, Joshua; Hoshitsuki, Keito; Huddart, Rachel; Caudle, Kelly E; Whirl-Carrillo, Michelle; Steyger, Peter S; Smith, Richard J H; Cody, Neal; Rodriguez-Antona, Cristina; Klein, Teri E; Newman, William G.
Afiliação
  • McDermott JH; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester University NHS Foundation Trust, Manchester, UK.
  • Wolf J; Division of Evolution and Genomic Sciences, School of Biological Sciences, University of Manchester, Manchester, UK.
  • Hoshitsuki K; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Huddart R; School of Pharmacy, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Caudle KE; Department of Biomedical Data Science, Stanford University, Stanford, California, USA.
  • Whirl-Carrillo M; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Steyger PS; Department of Biomedical Data Science, Stanford University, Stanford, California, USA.
  • Smith RJH; Translational Hearing Center, Biomedical Sciences, Creighton University, National Center for Rehabilitative Auditory Research, VA Portland Health Care System, Portland, Oregon, USA.
  • Cody N; Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, Internal Medicine (Nephrology), Pediatrics and Molecular Physiology & Biophysics, University of Iowa, Iowa City, Iowa, USA.
  • Rodriguez-Antona C; Department of Genetics and Genomic Sciences, Ichan School of Medicine at Mount Sinai, New York, New York, USA.
  • Klein TE; Sema4, Stamford, Connecticut, USA.
  • Newman WG; Hereditary Endocrine Cancer Group, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Clin Pharmacol Ther ; 111(2): 366-372, 2022 02.
Article em En | MEDLINE | ID: mdl-34032273
ABSTRACT
Aminoglycosides are widely used antibiotics with notable side effects, such as nephrotoxicity, vestibulotoxicity, and sensorineural hearing loss (cochleotoxicity). MT-RNR1 is a gene that encodes the 12s rRNA subunit and is the mitochondrial homologue of the prokaryotic 16s rRNA. Some MT-RNR1 variants (i.e., m.1095T>C; m.1494C>T; m.1555A>G) more closely resemble the bacterial 16s rRNA subunit and result in increased risk of aminoglycoside-induced hearing loss. Use of aminoglycosides should be avoided in individuals with an MT-RNR1 variant associated with an increased risk of aminoglycoside-induced hearing loss unless the high risk of permanent hearing loss is outweighed by the severity of infection and safe or effective alternative therapies are not available. We summarize evidence from the literature supporting this association and provide therapeutic recommendations for the use of aminoglycosides based on MT-RNR1 genotype (updates at https//cpicpgx.org/guidelines/ and www.pharmgkb.org).
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Ribossômico / Variantes Farmacogenômicos / Aminoglicosídeos / Perda Auditiva Neurossensorial / Antibacterianos Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Ribossômico / Variantes Farmacogenômicos / Aminoglicosídeos / Perda Auditiva Neurossensorial / Antibacterianos Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article