首页> 外文期刊>Environmental research >Alzheimer's disease and alpha-synuclein pathology in the olfactory bulbs of infants, children, teens and adults ≤ 40 years in Metropolitan Mexico City. APOE4 carriers at higher risk of suicide accelerate their olfactory bulb pathology
【24h】

Alzheimer's disease and alpha-synuclein pathology in the olfactory bulbs of infants, children, teens and adults ≤ 40 years in Metropolitan Mexico City. APOE4 carriers at higher risk of suicide accelerate their olfactory bulb pathology

机译:墨西哥大都会城市≤40岁的婴儿,儿童,青少年和成人的嗅球中的阿尔茨海默氏病和α-突触核蛋白病理学。自杀风险较高的APOE4携带者会加速其嗅球病变

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

There is growing evidence that air pollution is a risk factor for a number of neurodegenerative diseases, most notably Alzheimer's (AD) and Parkinson's (PD). It is generally assumed that the pathology of these diseases arises only later in life and commonly begins within olfactory eloquent pathways prior to the onset of the classical clinical symptoms. The present study demonstrates that chronic exposure to high levels of air pollution results in AD- and PD-related pathology within the olfactory bulbs of children and relatively young adults ages 11 months to 40 years. The olfactory bulbs (OBs) of 179 residents of highly polluted Metropolitan Mexico City (MMC) were evaluated for AD- and alpha-synuclein-related pathology. Even in toddlers, hyperphosphorylated tau (hTau) and Lewy neurites (LN) were identified in the OBs. By the second decade, 84% of the bulbs exhibited hTau (48/57), 68% LNs and vascular amyloid (39/57) and 36% (21/57) diffuse amyloid plaques. OB active endothelial phagocytosis of red blood cell fragments containing combustion-derived nanoparticles (CDNPs) and the neurovascular unit damage were associated with myelinated and unmyelinated axonal damage. OB hTau neurites were associated mostly with pretangle stages la and lb in subjects = 20 years of age, strongly suggesting olfactory deficits could potentially be an early guide of AD pretangle subcortical and cortical hTau. APOE4 versus APOE3 carriers were 6-13 times more likely to exhibit OB vascular amyloid, neuronal amyloid accumulation, alphasynuclein aggregates, hTau neurofibrillary tangles, and neurites. Remarkably, APOE4 carriers were 4.57 times more likely than non-carriers to die by suicide. The present findings, along with previous data that over a third of clinically healthy MMC teens and young adults exhibit low scores on an odor identification test, support the concept that olfactory testing may aid in identifying young people at high risk for neurodegenerative diseases. Moreover, results strongly support early neuroprotective interventions in fine particulate matter (PM2.5) and CDNP's exposed individuals = 20 years of age, and the critical need for air pollution control.
机译:越来越多的证据表明,空气污染是许多神经退行性疾病的危险因素,最显着的是阿尔茨海默氏症(AD)和帕金森氏症(PD)。通常认为,这些疾病的病理仅在生命的晚期出现,并且通常在经典临床症状发作之前在嗅觉雄性途径中开始。本研究表明,长期暴露于高水平的空气污染会导致11个月至40岁的儿童和相对年轻的成年人的嗅球内出现AD和PD相关的病理。对179名高度污染的墨西哥大都市(MMC)居民的嗅球(OB)进行了AD和α-突触核蛋白相关病理的评估。即使在幼儿中,在OB中也发现了高磷酸化的tau(hTau)和路易神经突(LN)。到第二个十年,84%的球茎表现出hTau(48/57),68%的LN和血管淀粉样蛋白(39/57)和36%(21/57)的弥散性淀粉样斑块。 OB活性内皮细胞吞噬的红细胞碎片包含燃烧衍生的纳米粒子(CDNPs)和神经血管单位的损害与髓鞘和未髓鞘的轴突损伤有关。在≤20岁的受试者中,OB hTau神经突主要与缠结前期la和lb相关,强烈暗示嗅觉缺陷可能是AD缠结前皮质下和皮质hTau的早期指南。 APOE4和APOE3携带者出现OB血管淀粉样蛋白,神经元淀粉样蛋白积累,α突触核蛋白聚集体,hTau神经原纤维缠结和神经突的可能性高6-13倍。值得注意的是,APOE4携带者自杀死亡的可能性是非携带者的4.57倍。目前的发现,以及以前的数据表明,超过三分之一的临床健康的MMC青少年和年轻人在气味识别测试中得分较低,支持了嗅觉测试可以帮助识别神经退行性疾病高风险年轻人的概念。此外,研究结果强烈支持对细颗粒物(PM2.5)和CDNP暴露个体(<= 20岁)的早期神经保护性干预,以及对空气污染控制的迫切需求。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号