Armstrong Nicole M, An Yang, Doshi Jimit, Erus Guray, Ferrucci Luigi, Davatzikos Christos, Deal Jennifer A, Lin Frank R, Resnick Susan M
Laboratory of Behavioral Neuroscience, National Institute on Aging, National Institutes of Health, Baltimore, Maryland.
Section of Biomedical Image Analysis, Department of Radiology, University of Pennsylvania, Philadelphia.
JAMA Otolaryngol Head Neck Surg. 2019 Sep 1;145(9):794-802. doi: 10.1001/jamaoto.2019.1610.
Hearing impairment (HI) in midlife (45-65 years of age) may be associated with longitudinal neurodegeneration of temporal lobe structures, a biomarker of early Alzheimer disease.
To evaluate the association of midlife HI with brain volume trajectories in later life (≥65 years of age).
DESIGN, SETTING, AND PARTICIPANTS: This prospective cohort study used data from the Baltimore Longitudinal Study of Aging to evaluate hearing from November 5, 1990, to October 3, 1994, and late-life volume change from July 10, 2008, to January 29, 2015, using magnetic resonance imaging (MRI) (mean follow-up time, 19.3 years). Data analysis was performed from September 22, 2017, to August 27, 2018. A total of 194 community-dwelling older adults who had midlife measures of peripheral hearing at a mean age of 54.5 years and late-life volume change of up to 6 years between the first and most recent MRI assessment were studied. Excluded were those with baseline cognitive impairment, stroke, head injuries, Parkinson disease, and bipolar disorder.
Hearing as measured with pure tone audiometry in each ear from November 5, 1990, to October 3, 1994, and late-life temporal lobe volume change measured by MRI.
Linear mixed-effects models with random intercepts were used to examine the association of midlife hearing (pure tone average of 0.5-4 kHz tones in the better ear and each ear separately) with longitudinal late-life MRI-based measures of temporal lobe structures (hippocampus, entorhinal cortex, parahippocampal gyrus, and superior, middle, and inferior temporal gyri) in the left and right hemispheres, in addition to global and lobar regions, adjusting for baseline demographic characteristics (age, sex, subsequent cognitive impairment status, and educational level) and intracranial volume.
A total of 194 patients (mean [SD] age at hearing assessment, 54.5 [10.0] years; 106 [54.6%] female; 169 [87.1%] white) participated in the study. After Bonferroni correction, poorer midlife hearing in the better ear was associated with steeper late-life volumetric declines in the right temporal gray matter (β = -0.113; 95% CI, -0.182 to -0.044), right hippocampus (β = -0.008; 95% CI, -0.012 to -0.004), and left entorhinal cortex (β = -0.009; 95% CI, -0.015 to -0.003). Poorer midlife hearing in the right ear was associated with steeper late-life volumetric declines in the right temporal gray matter (β = -0.136; 95% CI, -0.197 to -0.075), right hippocampus (β = -0.008; 95% CI, -0.012 to -0.004), and left entorhinal cortex (β = -0.009; 95% CI, -0.015 to -0.003), whereas there were no associations between poorer midlife hearing in the left ear with late-life volume loss.
The findings suggest that midlife HI is a risk factor for temporal lobe volume loss. Poorer midlife hearing, particularly in the right ear, was associated with declines in hippocampus and entorhinal cortex.
中年(45 - 65岁)听力障碍(HI)可能与颞叶结构的纵向神经退行性变有关,而颞叶结构是早期阿尔茨海默病的一个生物标志物。
评估中年HI与晚年(≥65岁)脑容量轨迹之间的关联。
设计、地点和参与者:这项前瞻性队列研究使用了巴尔的摩纵向衰老研究的数据,于1990年11月5日至1994年10月3日评估听力,并于2008年7月10日至2015年1月29日使用磁共振成像(MRI)评估晚年的脑容量变化(平均随访时间为19.3年)。数据分析于2017年9月22日至2018年8月27日进行。共研究了194名社区居住的老年人,他们在平均年龄54.5岁时进行了中年外周听力测量,并且在首次和最近一次MRI评估之间有长达6年的晚年脑容量变化。排除了那些有基线认知障碍、中风、头部受伤、帕金森病和双相情感障碍的人。
1990年11月5日至1994年10月3日期间用纯音听力计测量的每只耳朵的听力,以及通过MRI测量的晚年颞叶体积变化。
使用具有随机截距的线性混合效应模型来检验中年听力(较好耳以及每只耳朵单独的0.5 - 4kHz纯音平均听阈)与基于MRI的晚年颞叶结构(海马体、内嗅皮质、海马旁回以及颞上回、颞中回和颞下回)在左右半球以及整体和脑叶区域的纵向测量之间的关联,并对基线人口统计学特征(年龄、性别、随后的认知障碍状态和教育水平)和颅内体积进行了校正。
共有来自194名患者(听力评估时的平均[标准差]年龄为54.5[10.0]岁;106名[54.6%]为女性;169名[87.1%]为白人)参与了该研究。经过Bonferroni校正后,较好耳中年听力较差与右侧颞叶灰质(β = -0.113;95%置信区间,-0.182至-0.044)、右侧海马体(β = -0.008;95%置信区间,-0.012至-0.004)和左侧内嗅皮质(β = -0.009;95%置信区间,-0.015至-0.003)的晚年体积下降幅度更大有关。右耳中年听力较差与右侧颞叶灰质(β = -0.136;95%置信区间,-0.197至-0.075)、右侧海马体(β = -0.008;95%置信区间,-0.012至-0.004)和左侧内嗅皮质(β = -0.009;95%置信区间,-0.015至-0.003)的晚年体积下降幅度更大有关,而左耳中年听力较差与晚年体积减少之间没有关联。
研究结果表明中年HI是颞叶体积减少的一个危险因素。中年听力较差,尤其是右耳听力较差,与海马体和内嗅皮质的体积下降有关。