Polygenic Risk Score-Based Association Analysis Identifies Genetic Comorbidities Associated with Age-Related Hearing Difficulty in Two Independent Samples.

IF 2.4 3区 医学 Q3 NEUROSCIENCES Jaro-Journal of the Association for Research in Otolaryngology Pub Date : 2024-08-01 Epub Date: 2024-05-23 DOI:10.1007/s10162-024-00947-0
Ishan Sunilkumar Bhatt, Juan Antonio Raygoza Garay, Srividya Grama Bhagavan, Valerie Ingalls, Raquel Dias, Ali Torkamani
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Abstract

Purpose: Age-related hearing loss is the most common form of permanent hearing loss that is associated with various health traits, including Alzheimer's disease, cognitive decline, and depression. The present study aims to identify genetic comorbidities of age-related hearing loss. Past genome-wide association studies identified multiple genomic loci involved in common adult-onset health traits. Polygenic risk scores (PRS) could summarize the polygenic inheritance and quantify the genetic susceptibility of complex traits independent of trait expression. The present study conducted a PRS-based association analysis of age-related hearing difficulty in the UK Biobank sample (N = 425,240), followed by a replication analysis using hearing thresholds (HTs) and distortion-product otoacoustic emissions (DPOAEs) in 242 young adults with self-reported normal hearing. We hypothesized that young adults with genetic comorbidities associated with age-related hearing difficulty would exhibit subclinical decline in HTs and DPOAEs in both ears.

Methods: A total of 111,243 participants reported age-related hearing difficulty in the UK Biobank sample (> 40 years). The PRS models were derived from the polygenic risk score catalog to obtain 2627 PRS predictors across the health spectrum. HTs (0.25-16 kHz) and DPOAEs (1-16 kHz, L1/L2 = 65/55 dB SPL, F2/F1 = 1.22) were measured on 242 young adults. Saliva-derived DNA samples were subjected to low-pass whole genome sequencing, followed by genome-wide imputation and PRS calculation. The logistic regression analyses were performed to identify PRS predictors of age-related hearing difficulty in the UK Biobank cohort. The linear mixed model analyses were performed to identify PRS predictors of HTs and DPOAEs.

Results: The PRS-based association analysis identified 977 PRS predictors across the health spectrum associated with age-related hearing difficulty. Hearing difficulty and hearing aid use PRS predictors revealed the strongest association with the age-related hearing difficulty phenotype. Youth with a higher genetic predisposition to hearing difficulty revealed a subclinical elevation in HTs and a decline in DPOAEs in both ears. PRS predictors associated with age-related hearing difficulty were enriched for mental health, lifestyle, metabolic, sleep, reproductive, digestive, respiratory, hematopoietic, and immune traits. Fifty PRS predictors belonging to various trait categories were replicated for HTs and DPOAEs in both ears.

Conclusion: The study identified genetic comorbidities associated with age-related hearing loss across the health spectrum. Youth with a high genetic predisposition to age-related hearing difficulty and other related complex traits could exhibit sub-clinical decline in HTs and DPOAEs decades before clinically meaningful age-related hearing loss is observed. We posit that effective communication of genetic risk, promoting a healthy lifestyle, and reducing exposure to environmental risk factors at younger ages could help prevent or delay the onset of age-related hearing difficulty at older ages.

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基于多基因风险评分的关联分析在两个独立样本中发现了与年龄相关听力障碍有关的遗传合并症。
目的:老年性听力损失是最常见的永久性听力损失,与各种健康特征相关,包括阿尔茨海默病、认知能力下降和抑郁症。本研究旨在确定老年性听力损失的遗传合并症。过去的全基因组关联研究发现了多个基因组位点与常见的成人发病健康特征有关。多基因风险评分(PRS)可以总结多基因遗传,并量化复杂性状的遗传易感性,而不受性状表达的影响。本研究对英国生物库样本(N = 425,240 )中与年龄相关的听力困难进行了基于多基因风险评分的关联分析,随后使用听阈(HTs)和失真产物耳声发射(DPOAEs)对 242 名自我报告听力正常的年轻人进行了重复分析。我们假设,患有与年龄相关的听力困难遗传合并症的年轻人会表现出双耳听阈和 DPOAEs 的亚临床下降:在英国生物库样本中,共有 111,243 名参与者报告了与年龄相关的听力障碍(大于 40 岁)。PRS模型来自多基因风险评分目录,获得了2627个健康范围内的PRS预测因子。对 242 名年轻成年人进行了 HTs(0.25-16 kHz)和 DPOAEs(1-16 kHz,L1/L2 = 65/55 dB SPL,F2/F1 = 1.22)测量。对唾液中的 DNA 样本进行了低通滤波全基因组测序,然后进行了全基因组归因和 PRS 计算。通过逻辑回归分析,确定了英国生物库队列中年龄相关听力障碍的 PRS 预测因子。进行线性混合模型分析以确定PRS预测HTs和DPOAEs的因素:基于 PRS 的关联分析确定了 977 个与年龄相关听力困难有关的健康范围内的 PRS 预测因子。听力困难和助听器使用 PRS 预测因子与年龄相关听力困难表型的关联性最强。听力困难遗传易感性较高的青少年的双耳 HTs 出现亚临床升高,DPOAEs 出现下降。与年龄相关听力障碍相关的 PRS 预测因子富含心理健康、生活方式、代谢、睡眠、生殖、消化、呼吸、造血和免疫特征。属于不同性状类别的 50 个 PRS 预测因子在双耳 HTs 和 DPOAEs 中得到了重复:结论:这项研究发现了与年龄相关性听力损失有关的遗传合并症。对老年性听力障碍和其他相关复杂特征具有高度遗传易感性的青少年,可能会在临床上观察到有意义的老年性听力损失之前几十年,就出现 HTs 和 DPOAEs 的亚临床衰退。我们认为,有效传达遗传风险信息、提倡健康的生活方式以及在年轻时减少接触环境风险因素,有助于预防或推迟老年性听力障碍的发生。
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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.
期刊最新文献
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