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J Alzheimers Dis. 2018;66(4):1437-1451. doi: 10.3233/JAD-180853.

Non-Phosphorylated Tau in Cerebrospinal Fluid is a Marker of Alzheimer's Disease Continuum in Young Urbanites Exposed to Air Pollution.

Author information

1
The University of Montana, Missoula, MT, USA.
2
Universidad del Valle de México, Mexico.
3
Department of Mathematics, Boise State University, Boise, ID, USA.
4
AJ Roboscreen GmbH, Leipzig, Germany.
5
Paul-Flechsig-Institute for Brain Research, Leipzig, Germany.
6
Instituto de Medicina Forense, Universidad Veracruzana, Boca del Rio, Mexico.
7
Neurofisiología Clínica, Hospital Español, Ciudad de México, Mexico.
8
Instituto Nacional de Pediatría, Mexico.

Abstract

Long-term exposure to fine particulate matter (PM2.5) and ozone (O3) above USEPA standards is associated with Alzheimer's disease (AD) risk. Metropolitan Mexico City (MMC) children exhibit subcortical pretangles in infancy and cortical tau pre-tangles, NFTs, and amyloid phases 1-2 by the 2nd decade. Given their AD continuum, we measured in 507 normal cerebrospinal fluid (CSF) samples (MMC 354, controls 153, 12.82±6.73 y), a high affinity monoclonal non-phosphorylated tau antibody (non-P-Tau), as a potential biomarker of AD and axonal damage. In 81 samples, we also measured total tau (T-Tau), tau phosphorylated at threonine 181 (P-Tau), amyloid-β1-42, BDNF, and vitamin D. We documented by electron microscopy myelinated axonal size and the pathology associated with combustion-derived nanoparticles (CDNPs) in anterior cingulate cortex white matter in 6 young residents (16.25±3.34 y). Non-P-Tau showed a strong increase with age significantly faster among MMC versus controls (p = 0.0055). Aβ1 - 42 and BDNF concentrations were lower in MMC children (p = 0.002 and 0.03, respectively). Anterior cingulate cortex showed a significant decrease (p = <0.0001) in the average axonal size and CDNPs were associated with organelle pathology. Significant age increases in non-P-Tau support tau changes early in a population with axonal pathology and evolving AD hallmarks in the first two decades of life. Non-P-Tau is an early biomarker of axonal damage and potentially valuable to monitor progressive longitudinal changes along with AD multianalyte classical CSF markers. Neuroprotection of young urbanites with PM2.5 and CDNPs exposures ought to be a public health priority to halt the development of AD in the first two decades of life.

KEYWORDS:

Alzheimer’s disease; Aβ1-42; BDNF; Mexico City; PM2.5; PrPC; Wallerian degeneration; air pollution; axonal damage; cerebrospinal fluid; children; combustion-derived nanoparticles; insulin; leptin; non-phosphorylated tau; vitamin D; white matter

PMID:
30412505
DOI:
10.3233/JAD-180853

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