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Exploring the Genetic Foundations of Speech-in-Noise Deficits: Implications for Practitioners

Exploring the Genetic Foundations of Speech-in-Noise Deficits: Implications for Practitioners

Speech-in-noise (SIN) deficits present a significant challenge for many individuals, even those with normal hearing thresholds. Recent research has shed light on the genetic underpinnings of these deficits, offering valuable insights for practitioners in the field of audiology and beyond. A genome-wide association study (GWAS) has revealed a complex polygenic architecture that could explain individual differences in SIN perception among those who self-report normal hearing.

The Genetic Landscape of SIN Deficits

The study involved 279,911 individuals from the UK Biobank cohort, identifying 996 single nucleotide polymorphisms (SNPs) across four genomic loci with significant associations to SIN deficits. Notably, these genetic signals were enriched in brain tissues such as the anterior cingulate cortex and hippocampus, highlighting the role of cognitive processing in SIN perception.

This research emphasizes that SIN deficits are not solely an auditory issue but involve complex interactions between auditory and cognitive systems. Cognitive traits like working memory and selective attention play crucial roles in processing speech amid background noise.

Implications for Audiology Practice

The findings from this GWAS can significantly impact clinical practice. Here are some ways practitioners can leverage this information:

The Role of Further Research

The study opens new avenues for research into the genetic basis of auditory processing disorders. Future studies could explore:

A Call to Action for Practitioners

This research underscores the importance of an interdisciplinary approach to managing SIN deficits. By integrating genetic insights with traditional audiological practices, practitioners can offer more comprehensive care to individuals struggling with these challenges. Moreover, staying informed about ongoing research and advancements in genetics will be crucial for developing effective interventions.

A genome-wide association study reveals a polygenic architecture of speech-in-noise deficits in individuals with self-reported normal hearing


Citation: Ishan Sunilkumar Bhatt et al., A genome-wide association study reveals a polygenic architecture of speech-in-noise deficits in individuals with self-reported normal hearing, Scientific Reports (2024). https://doi.org/10.1038/s41598-024-63972-2
Marnee Brick, President, TinyEYE Therapy Services

Author's Note: Marnee Brick, TinyEYE President, and her team collaborate to create our blogs. They share their insights and expertise in the field of Speech-Language Pathology, Online Therapy Services and Academic Research.

Connect with Marnee on LinkedIn to stay updated on the latest in Speech-Language Pathology and Online Therapy Services.

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