Polygenic Risk Score-Based Association Analysis of Speech-in-Noise and Hearing Threshold Measures in Healthy Young Adults with Self-reported Normal Hearing

Purpose Speech-in-noise (SIN) traits exhibit high inter-subject variability, even for healthy young adults reporting normal hearing. Emerging evidence suggests that genetic variability could influence inter-subject variability in SIN traits. Genome-wide association studies (GWAS) have uncovered the...

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Veröffentlicht in:Journal of the Association for Research in Otolaryngology 2023-10, Vol.24 (5), p.513-525
Hauptverfasser: Bhatt, Ishan Sunilkumar, Ramadugu, Sai Kumar, Goodman, Shawn, Bhagavan, Srividya Grama, Ingalls, Valerie, Dias, Raquel, Torkamani, Ali
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Sprache:eng
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Zusammenfassung:Purpose Speech-in-noise (SIN) traits exhibit high inter-subject variability, even for healthy young adults reporting normal hearing. Emerging evidence suggests that genetic variability could influence inter-subject variability in SIN traits. Genome-wide association studies (GWAS) have uncovered the polygenic architecture of various adult-onset complex human conditions. Polygenic risk scores (PRS) summarize complex genetic susceptibility to quantify the degree of genetic risk for health conditions. The present study conducted PRS-based association analyses to identify PRS risk factors for SIN and hearing threshold measures in 255 healthy young adults (18–40 years) with self-reported normal hearing. Methods Self-reported SIN perception abilities were assessed by the Speech, Spatial, and Qualities of Hearing Scale (SSQ12). QuickSIN and audiometry (0.25–16 kHz) were performed on 218 participants. Saliva-derived DNA was used for low-pass whole genome sequencing, and 2620 PRS variables for various traits were calculated using the models derived from the polygenic risk score (PGS) catalog. The regression analysis was conducted to identify predictors for SSQ12, QuickSIN, and better ear puretone averages at conventional (PTA 0.5–2 ), high (PTA 4-8 ), and extended-high (PTA 12.5–16 ) frequency ranges. Results Participants with a higher genetic predisposition to HDL cholesterol reported better SSQ12. Participants with high PRS to dementia revealed significantly elevated PTA 4-8 , and those with high PRS to atrial fibrillation and flutter revealed significantly elevated PTA 12.5–16 . Conclusion These results indicate that healthy individuals with polygenic risk of certain health conditions could exhibit a subclinical decline in hearing health measures at young ages, decades before clinically meaningful SIN deficits and hearing loss could be observed. PRS could be used to identify high-risk individuals to prevent hearing health conditions by promoting a healthy lifestyle.
ISSN:1438-7573
1525-3961
1438-7573
DOI:10.1007/s10162-023-00911-4