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Review
. 2017 May 8:11:236.
doi: 10.3389/fnins.2017.00236. eCollection 2017.

Genetics of Tinnitus: Still in its Infancy

Affiliations
Review

Genetics of Tinnitus: Still in its Infancy

Barbara Vona et al. Front Neurosci. .

Abstract

Tinnitus is the perception of a phantom sound that affects between 10 and 15% of the general population. Despite this considerable prevalence, treatments for tinnitus are presently lacking. Tinnitus exhibits a diverse array of recognized risk factors and extreme clinical heterogeneity. Furthermore, it can involve an unknown number of auditory and non-auditory networks and molecular pathways. This complex combination has hampered advancements in the field. The identification of specific genetic factors has been at the forefront of several research investigations in the past decade. Nine studies have examined genes in a case-control association approach. Recently, a genome-wide association study has highlighted several potentially significant pathways that are implicated in tinnitus. Two twin studies have calculated a moderate heritability for tinnitus and disclosed a greater concordance rate in monozygotic twins compared to dizygotic twins. Despite the more recent data alluding to genetic factors in tinnitus, a strong association with any specific genetic locus is lacking and a genetic study with sufficient statistical power has yet to be designed. Future research endeavors must overcome the many inherent limitations in previous study designs. This review summarizes the previously embarked upon tinnitus genetic investigations and summarizes the hurdles that have been encountered. The identification of candidate genes responsible for tinnitus may afford gene based diagnostic approaches, effective therapy development, and personalized therapeutic intervention.

Keywords: complex disorders; genetic heterogeneity; genetics; genome-wide association study (GWAS); hearing loss; tinnitus; twin study.

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Figures

Figure 1
Figure 1
A timeline overview of the genetic research in tinnitus that has been conducted to date. Single genes that were studied via candidate gene association analysis are boxed with a solid black line and represent the majority of work performed in the genetics of tinnitus. All other studies are boxed with a dotted black line.

References

    1. Ambrosini A., D'Onofrio M., Grieco G. S., Di Mambro A., Montagna G., Fortini D., et al. (2005). Familial basilar migraine associated with a new mutation in the ATP1A2 gene. Neurology 65, 1826–1828. 10.1212/01.wnl.0000187072.71931.c0 - DOI - PubMed
    1. Badenhop R. F., Cherian S., Lord R. S., Baysal B. E., Taschner P. E., Schofield P. R. (2001). Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss. Genes Chromosomes Cancer 31, 255–263. 10.1002/gcc.1142 - DOI - PubMed
    1. Baguley D., McFerran D., Hall D. (2013). Tinnitus. Lancet 382, 1600–1607. 10.1016/S0140-6736(13)60142-7 - DOI - PubMed
    1. Baldo P., Doree C., Molin P., McFerran D., Cecco S. (2012). Antidepressants for patients with tinnitus. Cochrane Database Syst. Rev. 12:Cd003853 10.1002/14651858.CD003853.pub3 - DOI - PMC - PubMed
    1. Bayley J. P., van Minderhout I., Weiss M. M., Jansen J. C., Oomen P. H., Menko F. H., et al. (2006). Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma. BMC Med. Genet. 7:1. 10.1186/1471-2350-7-1 - DOI - PMC - PubMed

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