SUPR
TIGER: tinnitus genetic and environmental risks
Dnr:

sens2019022

Type:

SNIC SENS

Principal Investigator:

Christopher Cederroth

Affiliation:

Karolinska Institutet

Start Date:

2019-11-30

End Date:

2025-01-01

Primary Classification:

40303: Clinical Science

Allocation

  • Castor /proj/nobackup at UPPMAX: 40000 GiB
  • Cygnus /proj/nobackup at UPPMAX: 40000 GiB
  • Castor /proj at UPPMAX: 5000 GiB
  • Cygnus /proj at UPPMAX: 5000 GiB
  • Bianca at UPPMAX: 10 x 1000 core-h/month

Abstract

Tinnitus is the most frequent phantom sensation, affecting 70 million individuals in Europe. It dramatically increases with age, with near 40% of the elderlies experiencing tinnitus. It can be severely debilitating, increasing the risk for sick leave, disability pension and even suicide. While prevalence is higher in men, women, shows greater psychological burden and loss of life quality, suggesting that different coping mechanisms operate in the two genders. From a genetic perspective, we recently found that specific forms of tinnitus displayed significant heritability in men, albeit when segregated according to age, young women showed such high genetic influences. On this basis, TIGER aims to provide three major insights needed for long-lasting prevention and therapy for tinnitus through the principal goals: i) the identification of environmental risk factors to define non-genetic risks of developing severe tinnitus; ii) the identification of novel genetic and blood biomarkers. The insights from the two first aims will be used to iii) stratify disease risk and elaborate preventive medical recommendations for high-risk subgroups of tinnitus patients and to define molecular drivers/biological pathways relevant for the development of severe tinnitus that will be used to identify and validate new therapeutic targets. Here, we will use epidemiological lifestyle, nutritional, and medical analytical data from large Swedish longitudinal and Italian retrospective studies, and molecular genetics, coupled to in-depth tinnitus phenotyping beyond current clinical practice.