Frailty and hearing loss: From association to causation

孟德尔随机化 全基因组关联研究 观察研究 医学 遗传关联 全国健康与营养检查调查 混淆 优势比 逻辑回归 人口学 单核苷酸多态性 内科学 肿瘤科 基因型 遗传学 环境卫生 人口 生物 遗传变异 社会学 基因
作者
Yun Liu,Peiyi Qian,Shuli Guo,Shuangyan Liu,Dahui Wang,Lei Yang
出处
期刊:Frontiers in Aging Neuroscience [Frontiers Media]
卷期号:14 被引量:3
标识
DOI:10.3389/fnagi.2022.953815
摘要

Observational studies suggest that frailty is associated with hearing loss (HL) but with inconsistent results. This study aims to examine such association and to assess its causality.The cross-sectional data from the National Health and Nutrition Examination Survey (NHANES). Multivariate logistic regression models were used to assess the association between HL and frailty index (FI). Genetic variants associated with the FI and HL were obtained from a large genome-wide association study (GWAS) meta-analysis and UK Biobank GWAS. The inverse variance weighting (IVW) method was used to estimate causal effects. Sensitivity analyses were performed to further validate the robustness of results.In this cross-sectional analysis, results support the possibility that frailty may be associated with a higher risk of developing HL, with self-reported [odds ratio (OR) = 2.813; 95% CI, 2.386, 3.317; p < 0.001], speech frequency HL (OR = 1.975; 95% CI, 1.679-2.323; p < 0.001), and high frequency HL (OR = 1.748; 95% CI, 1.459-2.094; p < 0.001). In the adjusted model, frail participants remained at high risk of HL. Mendelian randomization (MR) studies showed a bidirectional causal association between genetically predicted FI and risk of HL (FI for exposure: OR = 1.051; 95% CI, 1.020-1.083; p = 0.001; HL for exposure: OR = 1.527; 95% CI, 1.227-1.901; p < 0.001).Our observational study found that inter-individual differences in frailty were associated with the risk of developing HL. Genetic evidence suggests a potential bidirectional causal association between FI and HL. Furthermore, the potential mechanisms of this association require investigation.

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