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

IF 2.4 3区 医学 Q3 NEUROSCIENCES Jaro-Journal of the Association for Research in Otolaryngology Pub Date : 2023-10-01 Epub Date: 2023-10-02 DOI:10.1007/s10162-023-00911-4
Ishan Sunilkumar Bhatt, Sai Kumar Ramadugu, Shawn Goodman, Srividya Grama Bhagavan, Valerie Ingalls, Raquel Dias, Ali Torkamani
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Abstract

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 (PTA0.5-2), high (PTA4-8), and extended-high (PTA12.5-16) frequency ranges.

Results: Participants with a higher genetic predisposition to HDL cholesterol reported better SSQ12. Participants with high PRS to dementia revealed significantly elevated PTA4-8, and those with high PRS to atrial fibrillation and flutter revealed significantly elevated PTA12.5-16.

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.

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自报听力正常的健康年轻人噪声中言语与听力阈值测量的基于多因素风险评分的关联分析。
目的:噪声中的言语(SIN)特征表现出很高的受试者间变异性,即使对于报告听力正常的健康年轻人来说也是如此。新出现的证据表明,遗传变异性可能影响SIN性状的个体间变异性。全基因组关联研究(GWAS)揭示了各种成人发病的复杂人类疾病的多基因结构。多基因风险评分(PRS)总结了复杂的遗传易感性,以量化健康状况的遗传风险程度。本研究对255名自我报告听力正常的健康年轻人(18-40岁)进行了基于PRS的关联分析,以确定SIN和听力阈值测量的PRS风险因素。方法:采用言语、空间和听力质量量表(SSQ12)评定自报SIN感知能力。对218名参与者进行了QuickSIN和听力测定(0.25-16kHz)。唾液来源的DNA用于低通全基因组测序,并使用多基因风险评分(PGS)目录中的模型计算了各种性状的2620个PRS变量。进行回归分析以确定SSQ12、QuickSIN和更好的耳纯音平均值在常规(PTA0.5-2)、高(PTA4-8)和扩展高(PTA12.5-16)频率范围的预测因素。结果:高密度脂蛋白胆固醇遗传易感性较高的参与者报告了更好的SSQ12。患有高PRS至痴呆症的参与者PTA4-8显著升高,患有高PRS-至心房颤动和扑动的参与者PTA12.5-16显著升高。结论:这些结果表明,患有某些健康状况的多基因风险的健康个体在年轻时可能表现出听力健康指标的亚临床下降,几十年前就可以观察到具有临床意义的SIN缺陷和听力损失。PRS可用于识别高危人群,通过促进健康的生活方式来预防听力健康状况。
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来源期刊
CiteScore
4.10
自引率
12.50%
发文量
57
审稿时长
6-12 weeks
期刊介绍: JARO is a peer-reviewed journal that publishes research findings from disciplines related to otolaryngology and communications sciences, including hearing, balance, speech and voice. JARO welcomes submissions describing experimental research that investigates the mechanisms underlying problems of basic and/or clinical significance. Authors are encouraged to familiarize themselves with the kinds of papers carried by JARO by looking at past issues. Clinical case studies and pharmaceutical screens are not likely to be considered unless they reveal underlying mechanisms. Methods papers are not encouraged unless they include significant new findings as well. Reviews will be published at the discretion of the editorial board; consult the editor-in-chief before submitting.
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