Department of Brain Sciences, Imperial College London, London, UK.
The Dementia Research Centre, Department of Neurodegenerative Disease, University College London, London, UK.
J Neurol Neurosurg Psychiatry. 2024 Aug 16;95(9):829-832. doi: 10.1136/jnnp-2023-333101.
Hearing loss has been proposed as a modifiable risk factor for dementia. However, the relationship between hearing, neurodegeneration, and cognitive change, and the extent to which pathological processes such as Alzheimer's disease and cerebrovascular disease influence these relationships, is unclear.
Data from 287 adults born in the same week of 1946 who underwent baseline pure tone audiometry (mean age=70.6 years) and two time point cognitive assessment/multimodal brain imaging (mean interval 2.4 years) were analysed. Hearing impairment at baseline was defined as a pure tone average of greater than 25 decibels in the best hearing ear. Rates of change for whole brain, hippocampal and ventricle volume were estimated from structural MRI using the Boundary Shift Integral. Cognition was assessed using the Pre-clinical Alzheimer's Cognitive Composite. Regression models were performed to evaluate how baseline hearing impairment associated with subsequent brain atrophy and cognitive decline after adjustment for a range of confounders including baseline β-amyloid deposition and white matter hyperintensity volume.
111 out of 287 participants had hearing impairment. Compared with those with preserved hearing, hearing impaired individuals had faster rates of whole brain atrophy, and worse hearing (higher pure tone average) predicted faster rates of hippocampal atrophy. In participants with hearing impairment, faster rates of whole brain atrophy predicted greater cognitive change. All observed relationships were independent of β-amyloid deposition and white matter hyperintensity volume.
Hearing loss may influence dementia risk via pathways distinct from those typically implicated in Alzheimer's and cerebrovascular disease in cognitively unimpaired older adults.
听力损失已被提出作为痴呆的可改变风险因素。然而,听力、神经退行性变和认知变化之间的关系,以及阿尔茨海默病和脑血管病等病理过程对这些关系的影响程度尚不清楚。
对 287 名出生于 1946 年同一周的成年人进行了基线纯音测听(平均年龄 70.6 岁)和两次认知评估/多模态脑成像(平均间隔 2.4 年),分析了数据。基线听力障碍定义为最佳听力耳的纯音平均听力损失大于 25 分贝。使用边界位移积分从结构 MRI 估计全脑、海马和脑室体积的变化率。使用临床前阿尔茨海默病认知综合指数评估认知。进行回归模型以评估基线听力障碍与随后的脑萎缩和认知下降之间的关联,调整了一系列混杂因素,包括基线β-淀粉样蛋白沉积和白质高信号体积。
287 名参与者中有 111 名患有听力障碍。与听力正常的人相比,听力受损的人全脑萎缩速度更快,听力下降(纯音平均听力损失更高)预示着海马萎缩速度更快。在听力受损的参与者中,全脑萎缩速度越快,认知变化越大。所有观察到的关系都独立于β-淀粉样蛋白沉积和白质高信号体积。
在认知正常的老年人中,听力损失可能通过与阿尔茨海默病和脑血管病通常涉及的途径不同的途径影响痴呆风险。