Kaiser Permanente Washington Health Research Institute, Seattle, WA, USA.
Herbert Wertheim School of Public Health and Human Longevity Science, University of California San Diego, San Diego, CA, USA.
J Alzheimers Dis. 2023;96(3):1163-1172. doi: 10.3233/JAD-230767.
Hearing loss is associated with cognitive decline and increased risk for Alzheimer's disease, but the basis of this association is not understood.
To determine whether hearing impairment is associated with advanced brain aging or altered microstructure in areas involved with auditory and cognitive processing.
130 participants, (mean 76.4±7.3 years; 65% women) of the Rancho Bernardo Study of Healthy Aging had a screening audiogram in 2003-2005 and brain magnetic resonance imaging in 2014-2016. Hearing ability was defined as the average pure tone threshold (PTA) at 500, 1000, 2000, and 4000 Hz in the better-hearing ear. Brain-predicted age difference (Brain-pad) was calculated as the difference between brain-predicted age based on a validated structural imaging biomarker of brain age, and chronological age. Regional diffusion metrics in temporal and frontal cortex regions were obtained from diffusion-weighted MRIs. Linear regression analyses adjusted for age, gender, education, and health-related measures.
PTAs were not associated with brain-PAD (β= 0.09; 95% CI: -0.084 to 0.243; p = 0.34). PTAs were associated with reduced restricted diffusion and increased free water diffusion primarily in right hemisphere temporal and frontal areas (restricted diffusion: βs = -0.21 to -0.30; 95% CIs from -0.48 to -0.02; ps < 0.03; free water: βs = 0.18 to 0.26; 95% CIs 0.01 to 0.438; ps < 0.04).
Hearing impairment is not associated with advanced brain aging but is associated with differences in brain regions involved with auditory processing and attentional control. It is thus possible that increased dementia risk associated with hearing impairment arises, in part, from compensatory brain changes that may decrease resilience.
听力损失与认知能力下降和阿尔茨海默病风险增加有关,但这种关联的基础尚不清楚。
确定听力障碍是否与大脑老化加速或听觉和认知处理相关区域的微观结构改变有关。
130 名参与者(平均年龄 76.4±7.3 岁,65%为女性)参加了 Rancho Bernardo 健康老龄化研究,他们在 2003-2005 年接受了听力筛查,在 2014-2016 年接受了脑部磁共振成像检查。听力能力定义为较好耳在 500、1000、2000 和 4000Hz 时的平均纯音阈值(PTA)。脑预测年龄差(Brain-pad)是根据脑年龄的验证结构成像生物标志物与实际年龄之间的差异计算得出的。从弥散加权磁共振成像中获得颞叶和额叶皮质区的局部弥散指标。线性回归分析调整了年龄、性别、教育和健康相关指标。
PTA 与脑-PAD 无相关性(β=0.09;95%CI:-0.084 至 0.243;p=0.34)。PTA 与右侧颞叶和额叶区域的限制扩散减少和自由水扩散增加有关(限制扩散:βs=-0.21 至-0.30;95%CI 从-0.48 到-0.02;p<0.03;自由水:βs=0.18 至 0.26;95%CI 为 0.01 至 0.438;p<0.04)。
听力障碍与大脑老化加速无关,但与听觉处理和注意力控制相关的大脑区域的差异有关。因此,听力障碍导致痴呆风险增加的原因,部分可能是由于代偿性的大脑变化,从而降低了大脑的弹性。