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Exploring the genetic relationship between hearing impairment and Alzheimer's disease.
Mitchell, Brittany L; Thorp, Jackson G; Evans, David M; Nyholt, Dale R; Martin, Nicholas G; Lupton, Michelle K.
Afiliação
  • Mitchell BL; School of Biomedical Science and Institute of Health and Biomedical Innovation, Faculty of Health Queensland University of Technology (QUT) Brisbane Queensland Australia.
  • Thorp JG; Department of Genetics and Computational Biology QIMR Berghofer Medical Research Institute Brisbane Queensland Australia.
  • Evans DM; Department of Genetics and Computational Biology QIMR Berghofer Medical Research Institute Brisbane Queensland Australia.
  • Nyholt DR; Faculty of Medicine University of Queensland Brisbane Queensland Australia.
  • Martin NG; The University of Queensland Diamantina Institute The University of Queensland Brisbane Queensland Australia.
  • Lupton MK; MRC Integrative Epidemiology Unit University of Bristol Bristol United Kingdom.
Alzheimers Dement (Amst) ; 12(1): e12108, 2020.
Article em En | MEDLINE | ID: mdl-33005726
ABSTRACT

INTRODUCTION:

Hearing loss has been identified as the potentially largest modifiable risk factor for Alzheimer's disease (AD), estimated to account for a similar increase in AD risk as the apolipoprotein E (APOE) gene.

METHODS:

We investigated the genetic relationship between hearing loss and AD, and sought evidence for a causal relationship.

RESULTS:

We found a significant genetic overlap between hearing impairment and AD and a polygenic risk score for AD was able to significantly predict hearing loss in an independent cohort. Additionally, regions of the genome involved in inflammation were identified to be shared between hearing difficulty and AD. However, causality tests found no significant evidence of a causal relationship between these traits in either direction.

DISCUSSION:

Overall, these results show that the relationship between hearing difficulty and AD may, in part, be due to shared genes and immune response pathways between the traits. However, currently available data do not support a causal relationship.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article