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Adverse outcome pathway for aminoglycoside ototoxicity in drug-resistant tuberculosis treatment.

Publication ,  Journal Article
Hong, H; Dooley, KE; Starbird, LE; Francis, HW; Farley, JE
Published in: Arch Toxicol
May 2019

Individuals treated for multidrug-resistant tuberculosis (MDR-TB) with aminoglycosides (AGs) in resource-limited settings often experience permanent hearing loss. However, AG ototoxicity has never been conceptually integrated or causally linked to MDR-TB patients' pre-treatment health condition. We sought to develop a framework that examines the relationships between pre-treatment conditions and AG-induced hearing loss among MDR-TB-infected individuals in sub-Saharan Africa. The adverse outcome pathway (AOP) approach was used to develop a framework linking key events (KEs) within a biological pathway that results in adverse outcomes (AO), which are associated with chemical perturbation of a molecular initiating event (MIE). This AOP describes pathways initiating from AG accumulation in hair cells, sound transducers of the inner ear immediately after AG administration. After administration, the drug catalyzes cellular oxidative stress due to overproduction of reactive oxygen species. Since oxidative stress inhibits mitochondrial protein synthesis, hair cells undergo apoptotic cell death, resulting in irreversible hearing loss (AO). We identified the following pre-treatment conditions that worsen the causal linkage between MIE and AO: HIV, malnutrition, aging, noise, smoking, and alcohol use. The KEs are: (1) nephrotoxicity, pre-existing hearing loss, and hypoalbuminemia that catalyzes AG accumulation; (2) immunodeficiency and antioxidant deficiency that trigger oxidative stress pathways; and (3) co-administration of mitochondrial toxic drugs that hinder mitochondrial protein synthesis, causing apoptosis. This AOP clearly warrants the development of personalized interventions for patients undergoing MDR-TB treatment. Such interventions (i.e., choosing less ototoxic drugs, scheduling frequent monitoring, modifying nutritional status, avoiding poly-pharmacy) will be required to limit the burden of AG ototoxicity.

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Published In

Arch Toxicol

DOI

EISSN

1432-0738

Publication Date

May 2019

Volume

93

Issue

5

Start / End Page

1385 / 1399

Location

Germany

Related Subject Headings

  • Tuberculosis, Multidrug-Resistant
  • Toxicology
  • Reactive Oxygen Species
  • Oxidative Stress
  • Ototoxicity
  • Humans
  • Hearing Loss
  • Hair Cells, Auditory
  • Apoptosis
  • Antitubercular Agents
 

Citation

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Hong, H., Dooley, K. E., Starbird, L. E., Francis, H. W., & Farley, J. E. (2019). Adverse outcome pathway for aminoglycoside ototoxicity in drug-resistant tuberculosis treatment. Arch Toxicol, 93(5), 1385–1399. https://doi.org/10.1007/s00204-019-02407-8
Hong, Hyejeong, Kelly E. Dooley, Laura E. Starbird, Howard W. Francis, and Jason E. Farley. “Adverse outcome pathway for aminoglycoside ototoxicity in drug-resistant tuberculosis treatment.Arch Toxicol 93, no. 5 (May 2019): 1385–99. https://doi.org/10.1007/s00204-019-02407-8.
Hong H, Dooley KE, Starbird LE, Francis HW, Farley JE. Adverse outcome pathway for aminoglycoside ototoxicity in drug-resistant tuberculosis treatment. Arch Toxicol. 2019 May;93(5):1385–99.
Hong, Hyejeong, et al. “Adverse outcome pathway for aminoglycoside ototoxicity in drug-resistant tuberculosis treatment.Arch Toxicol, vol. 93, no. 5, May 2019, pp. 1385–99. Pubmed, doi:10.1007/s00204-019-02407-8.
Hong H, Dooley KE, Starbird LE, Francis HW, Farley JE. Adverse outcome pathway for aminoglycoside ototoxicity in drug-resistant tuberculosis treatment. Arch Toxicol. 2019 May;93(5):1385–1399.
Journal cover image

Published In

Arch Toxicol

DOI

EISSN

1432-0738

Publication Date

May 2019

Volume

93

Issue

5

Start / End Page

1385 / 1399

Location

Germany

Related Subject Headings

  • Tuberculosis, Multidrug-Resistant
  • Toxicology
  • Reactive Oxygen Species
  • Oxidative Stress
  • Ototoxicity
  • Humans
  • Hearing Loss
  • Hair Cells, Auditory
  • Apoptosis
  • Antitubercular Agents