4.4 Article

The relationship between subcortical tau pathology and Alzheimer's disease

Journal

BIOCHEMICAL SOCIETY TRANSACTIONS
Volume 40, Issue -, Pages 711-715

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/BST20120034

Keywords

Alzheimer's disease (AD); Braak stages; brainstem; neuropathology; subcortical; tau pathology

Funding

  1. Newcastle National Institute of Health Research Biomedical Research Centre In Ageing and Age-Related Diseases
  2. Dunhill Medical Trust [R173/1110]
  3. Medical Research Council [G0400074]
  4. National Institute of Health Research Biomedical Research Centre for Ageing and Age-Related Disease
  5. Alzheimers Research UK [ART-EG2010A-1] Funding Source: researchfish
  6. Medical Research Council [G0400074, G1100540, G0900652, G0502157] Funding Source: researchfish
  7. The Dunhill Medical Trust [R173/1110] Funding Source: researchfish
  8. MRC [G1100540, G0400074, G0502157, G0900652] Funding Source: UKRI

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The stepwise progression of tau pathology [NFTs (neurofibrillary tangles) and NTs (neuropil threads)] in AD (Alzheimer's disease) is generally assumed to begin in the transentorhinal region (entorhinal stage) from which it progresses to the hippocampus (limbic stage) and to neocortical regions (neocortical stage). This stepwise progression is reflected in the NFT Braak stages. However, it has been shown recently that tau pathology is frequently seen in subcortical nuclei, in particular the LC (locus coeruleus) in over 90% of individuals under 30 years of age, suggesting that AD-associated tau pathology begins in the LC and not in the transentorhinal region. On the other hand, only minimal amounts of tau pathology are seen in the LC in cases with considerable entorhinal tau pathology, while the severity of tau pathology in the LC significantly increases with increasing NFT Braak stages. These findings suggest that the LC becomes increasingly involved during AD progression rather than representing the site initially affected. Further studies are warranted to answer the question of whether tau pathology in the LC of young individuals is associated with AD or whether it rather reflects non-specific neuronal damage.

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