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听力损伤与痴呆和认知功能的关系:一项孟德尔随机化研究。

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

机构信息

Department of Neurology, Xuanwu Hospital, Capital Medical University, Changchun Street 45, Beijing, China.

出版信息

Alzheimers Res Ther. 2024 Oct 9;16(1):215. doi: 10.1186/s13195-024-01586-6.

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.

摘要

背景

大量观察性研究表明,听力障碍与痴呆之间存在关联,但因果关系和潜在机制仍不确定。本研究旨在使用两样本 Mendelian 随机化(MR)分析来探究听力障碍及其亚型与痴呆和认知功能之间的因果关系。

方法

我们进行了两样本 MR 分析,以检查听力障碍及其亚型(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[SIHL])对六种痴呆表型(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)和四种认知功能的因果影响。此外,还进行了多变量 MR(MVMR)分析,以探究潜在的中介机制。

结果

遗传决定的 CSHL 与 DLB(比值比[OR]1.69;95%置信区间[CI]1.08 至 2.63;P=0.021)和 FTD(OR 1.66;1.04 至 2.67;P=0.035)的风险增加相关,但与 AD(P=0.958)无关。遗传易感性导致 CHL 与 AD(OR 1.07;1.01 至 1.14;P=0.031)的风险增加有关。遗传决定的 SHL 与语义性痴呆(OR 3.81;1.09 至 13.37;P=0.037)的风险增加有关。遗传预测的 CHL 和 SIHL 均与一般认知表现(β-0.015 和-0.043;P=0.007 和 0.013)和流体智力评分(β-0.045 和-0.095;P=0.037 和 0.040)降低有关。在 MVMR 分析中,听力障碍与痴呆之间的因果关系通过孤独感、抑郁情绪和大脑皮质体积(尤其是内侧颞叶)介导,但不通过衰老或缺血性中风介导。

结论

总体而言,本研究提供了证据支持听力障碍与不同类型痴呆(包括 AD、FTD 和 DLB)风险增加以及一般认知功能下降之间存在因果关系。这些发现强调了将听力障碍作为可改变的痴呆风险因素进行干预的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/11462771/f83cd82a9e9b/13195_2024_1586_Fig1_HTML.jpg

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