Relationship between hearing impairment and dementia and cognitive function: a Mendelian randomization study.

IF 7.9 1区 医学 Q1 CLINICAL NEUROLOGY Alzheimer's Research & Therapy Pub Date : 2024-10-09 DOI:10.1186/s13195-024-01586-6
Deming Jiang, Jiahui Hou, Haitian Nan, Ailing Yue, Min Chu, Yihao Wang, Yingtao Wang, Liyong Wu
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Abstract

Background: There is a substantial body of observational research indicating an association between hearing impairment and dementia, yet the causal relationship and underlying mechanisms remain uncertain. This study aims to investigate the causal relationship between hearing impairment and its subtypes with dementia and cognitive function using two-sample Mendelian randomization (MR) analysis.

Methods: We performed two-sample MR analysis to examine the causal effects of hearing impairment and its subtypes, including conductive and sensorineural hearing loss (CSHL), conductive hearing loss (CHL), sensorineural hearing loss (SHL), and sudden sensorineural hearing loss (SIHL), on six dementia phenotypes (overall dementia, Alzheimer's disease [AD], Lewy body dementia [DLB], frontotemporal dementia [FTD], Parkinson's disease dementia, and vascular dementia) and four cognitive functions. Additionally, multivariable MR (MVMR) analysis was employed to investigate potential mediating mechanisms.

Results: Genetically determined CSHL was associated with an elevated risk of DLB (odds ratio [OR] 1.69; 95% CI 1.08 to 2.63; P = 0.021) and FTD (OR 1.66; 1.04 to 2.67; P = 0.035), but not AD (P = 0.958). Genetic predisposition to CHL was found to link with increased risks of AD (OR 1.07; 1.01 to 1.14; P = 0.031). Genetically determined SHL was causally associated with an elevated risk of semantic dementia (OR 3.81; 1.09 to 13.37; P = 0.037). Genetically predicted CHL and SIHL were both causally associated with lower general cognitive performance (β -0.015 and - 0.043; P = 0.007 and 0.013) and fluid intelligence score (β -0.045 and - 0.095; P = 0.037 and 0.040). In MVMR analysis, the causal relationship between hearing impairment and dementia was mediated by loneliness, depressed mood, and brain cortical volume, particularly the medial temporal lobe, but not by aging or ischemic stroke.

Conclusion: Overall, the study provides evidence supporting a causal relationship between hearing impairment and increased risks of different types of dementia (including AD, FTD, and DLB), as well as poorer general cognitive function. These findings underscore the importance of addressing hearing impairment as a modifiable risk factor for dementia.

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听力障碍与痴呆症和认知功能之间的关系:孟德尔随机研究。
背景:大量观察性研究表明,听力障碍与痴呆症之间存在关联,但其因果关系和内在机制仍不确定。本研究旨在利用双样本孟德尔随机分析法(MR)研究听力损伤及其亚型与痴呆症和认知功能之间的因果关系:我们进行了双样本 MR 分析,以研究听力损伤及其亚型(包括传导性和感音神经性听力损失(CSHL)、传导性听力损失(CHL)、感音神经性听力损失(SHL)和突发性感音神经性听力损失(SHL))的因果效应、和突发性感音神经性听力损失(SIHL),以及六种痴呆表型(总体痴呆、阿尔茨海默病[AD]、路易体痴呆[DLB]、额颞叶痴呆[FTD]、帕金森病痴呆和血管性痴呆)和四种认知功能。此外,还采用了多变量磁共振(MVMR)分析来研究潜在的中介机制:基因决定的CHL与DLB(几率比[OR]1.69;95% CI 1.08至2.63;P = 0.021)和FTD(OR 1.66;1.04至2.67;P = 0.035)风险升高有关,但与AD无关(P = 0.958)。研究发现,CHL的遗传易感性与AD的风险增加有关(OR 1.07;1.01至1.14;P = 0.031)。由基因决定的SHL与语义痴呆风险升高有因果关系(OR 3.81;1.09 至 13.37;P = 0.037)。遗传预测的 CHL 和 SIHL 与较低的一般认知能力(β -0.015 和 -0.043;P = 0.007 和 0.013)和流体智力得分(β -0.045 和 -0.095;P = 0.037 和 0.040)均有因果关系。在MVMR分析中,听力障碍与痴呆之间的因果关系是由孤独、抑郁情绪和大脑皮质体积(尤其是颞叶内侧)介导的,而不是由衰老或缺血性中风介导的:总之,该研究提供的证据支持了听力障碍与不同类型痴呆症(包括注意力缺失症、FTD 和 DLB)风险增加以及一般认知功能较差之间的因果关系。这些发现强调了将听力障碍作为痴呆症的一个可改变的风险因素的重要性。
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来源期刊
Alzheimer's Research & Therapy
Alzheimer's Research & Therapy 医学-神经病学
CiteScore
13.10
自引率
3.30%
发文量
172
审稿时长
>12 weeks
期刊介绍: Alzheimer's Research & Therapy is an international peer-reviewed journal that focuses on translational research into Alzheimer's disease and other neurodegenerative diseases. It publishes open-access basic research, clinical trials, drug discovery and development studies, and epidemiologic studies. The journal also includes reviews, viewpoints, commentaries, debates, and reports. All articles published in Alzheimer's Research & Therapy are included in several reputable databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, MEDLINE, PubMed, PubMed Central, Science Citation Index Expanded (Web of Science) and Scopus.
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