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A multi-hit hypothesis for an APOE4-dependent pathophysiological state

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posted on 2023-06-15, 20:39 authored by Oliver SteeleOliver Steele, Alex StuartAlex Stuart, Lucy Minkley, Kira Shaw, Orla Bonnar, Silvia Anderle, Andrew PennAndrew Penn, Jennifer Rusted, Louise SerpellLouise Serpell, Catherine HallCatherine Hall, Sarah KingSarah King
The APOE gene encoding the Apolipoprotein E protein is the single most significant genetic risk factor for late-onset Alzheimer's disease. The APOE4 genotype confers a significantly increased risk relative to the other two common genotypes APOE3 and APOE2. Intriguingly, APOE4 has been associated with neuropathological and cognitive deficits in the absence of Alzheimer's disease-related amyloid or tau pathology. Here, we review the extensive literature surrounding the impact of APOE genotype on central nervous system dysfunction, focussing on preclinical model systems and comparison of APOE3 and APOE4, given the low global prevalence of APOE2. A multi-hit hypothesis is proposed to explain how APOE4 shifts cerebral physiology towards pathophysiology through interconnected hits. These hits include the following: neurodegeneration, neurovascular dysfunction, neuroinflammation, oxidative stress, endosomal trafficking impairments, lipid and cellular metabolism disruption, impaired calcium homeostasis and altered transcriptional regulation. The hits, individually and in combination, leave the APOE4 brain in a vulnerable state where further cumulative insults will exacerbate degeneration and lead to cognitive deficits in the absence of Alzheimer's disease pathology and also a state in which such pathology may more easily take hold. We conclude that current evidence supports an APOE4 multi-hit hypothesis, which contributes to an APOE4 pathophysiological state. We highlight key areas where further study is required to elucidate the complex interplay between these individual mechanisms and downstream consequences, helping to frame the current landscape of existing APOE-centric literature.

History

Publication status

  • Published

File Version

  • Published version

Journal

Eur J Neurosci

ISSN

0953-816X

Publisher

Wiley

Event location

France

Department affiliated with

  • Neuroscience Publications

Full text available

  • Yes

Peer reviewed?

  • Yes

Legacy Posted Date

2022-06-14

First Open Access (FOA) Date

2022-06-14

First Compliant Deposit (FCD) Date

2022-06-13

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