The University of Montana, Missoula, MT, USA.
Universidad del Valle de México, México.
J Alzheimers Dis. 2019;70(4):1275-1286. doi: 10.3233/JAD-190405.
A major impediment in early diagnosis of Alzheimer's disease (AD) is the lack of robust non-invasive biomarkers of early brain dysfunction. Metropolitan Mexico City (MMC) children and young adults show hyperphosphorylated tau, amyloid-β, and α-synuclein within auditory and vestibular nuclei and marked dysmorphology in the ventral cochlear nucleus and superior olivary complex. Based on early involvement of auditory brainstem centers, we believe brainstem auditory evoked potentials can provide early AD biomarkers in MMC young residents. We measured brainstem auditory evoked potentials in MMC clinically healthy children (8.52±3.3 years) and adults (21.08±3.0 years, 42.48±8.5 years, and 71.2±6.4 years) compared to clean air controls (6.5±0.7 years) and used multivariate analysis adjusting for age, gender, and residency. MMC children had decreased latency to wave I, delays in waves III and V, and longer latencies for interwave intervals, consistent with delayed central conduction time of brainstem neural transmission. In sharp contrast, young adults have significantly shortened interwave intervals I-III and I-V. By the 5th decade, wave V and interval I-V were significantly shorter, while the elderly cohort had significant delay in mean latencies and interwave intervals. Compensatory plasticity, increased auditory gain, cochlear synaptopathy, neuroinflammation, and AD continuum likely play a role in the evolving distinct auditory pathology in megacity urbanites. Understanding auditory central and peripheral dysfunction in the AD continuum evolving and progressing in pediatric and young adult populations may shed light on the complex mechanisms of AD development and help identify strong noninvasive biomarkers. AD evolving from childhood in air pollution environments ought to be preventable.
阿尔茨海默病(AD)早期诊断的主要障碍是缺乏早期大脑功能障碍的稳健非侵入性生物标志物。墨西哥城大都市区(MMC)的儿童和年轻人在听觉和前庭核中显示出过度磷酸化的 tau、淀粉样蛋白-β 和 α-突触核蛋白,并在腹侧耳蜗核和上橄榄复合体中表现出明显的畸形。基于听觉脑干中心的早期参与,我们相信脑干听觉诱发电位可以为 MMC 年轻居民提供 AD 的早期生物标志物。我们测量了 MMC 临床健康儿童(8.52±3.3 岁)和成年人(21.08±3.0 岁、42.48±8.5 岁和 71.2±6.4 岁)的脑干听觉诱发电位,并与清洁空气对照组(6.5±0.7 岁)进行了比较,并使用多元分析调整了年龄、性别和居住地。MMC 儿童的 I 波潜伏期缩短,III 波和 V 波延迟,I-III 和 I-V 波间隔潜伏期延长,与脑干神经传递的中枢传导时间延迟一致。相比之下,年轻成年人的 I-III 和 I-V 波间隔明显缩短。到了 5 十年代,V 波和 I-V 波间隔明显缩短,而老年组的平均潜伏期和波间隔潜伏期明显延迟。代偿性可塑性、听觉增益增加、耳蜗突触病、神经炎症和 AD 连续体可能在大城市居民不断发展的独特听觉病理学中发挥作用。了解 AD 连续体中儿童和年轻成人中不断发展和进展的听觉中枢和周围功能障碍,可能有助于阐明 AD 发展的复杂机制,并有助于确定强大的非侵入性生物标志物。在污染环境中从儿童期开始的 AD 应该是可以预防的。