Association between hearing loss and hereditary ATTR amyloidosis

Amyloid. 2019 Dec;26(4):234-242. doi: 10.1080/13506129.2019.1663814. Epub 2019 Sep 10.

Abstract

Background: Hereditary transthyretin (TTR) related amyloidosis (ATTRv) is a life-threatening condition, which can potentially affect all organs. The objective was to identify the hearing status of patients with cardiac ATTRv and describe their audiological pattern. Methods: Nineteen patients with confirmed diagnosis of ATTRv cardiac amyloidosis (CA) underwent otoscopy and audiological tests, including pure tone and speech audiometry. Results: 74% were male, with a mean age of 72 ± 1.8 years. The main mutations were Val122Ile (n = 7) and Val30Met (n = 6). Objective hearing loss was detected in 17 patients (89%), whereas only 37% complained of hearing loss. ATTRv patients presented a different audiometric profile compared to patients of the same age with presbycusis: a higher prevalence and worse hearing thresholds compared to age-related expectations (ISO). Hearing loss affected all frequencies with, unexpectedly, mixed or conductive hearing loss (35%). According to the type of mutation, there was an increased rate of sensorineural or mixed/conductive hearing loss. Conclusions: the present study indicates that hearing loss is more prevalent and worse in patients with ATTRv amyloidosis than in the general population, while mostly clinically under-estimated. It suggests that ATTRv deposits could infiltrate the various anatomical structures of the inner and mild ear.

Keywords: cardiac amyloidosis; hearing loss; hereditary Transthyretin related amyloidosis (ATTRv); screening; transthyretin.

Publication types

  • Observational Study

MeSH terms

  • Amyloid Neuropathies, Familial / complications*
  • Amyloid Neuropathies, Familial / genetics
  • Female
  • Hearing Loss / complications*
  • Hearing Loss / genetics
  • Heart Diseases / complications*
  • Heart Diseases / genetics
  • Humans
  • Male
  • Prospective Studies

Supplementary concepts

  • Amyloidosis, Hereditary, Transthyretin-Related