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Emerging therapeutics and future insights into the pathobiology of Alzheimer’s disease

By: Irfan Ullah, Sang-Kyung Lee

Key Words: Alzheimer’s disease, Amyloid beta, Apolipoprotein E4, Immunotherapy, Tau.

Int. J. Biosci. 12(2), 232-247, February 2018.

DOI: http://dx.doi.org/10.12692/ijb/12.2.232-247

Certification: ijb 2018 0250 [Generate Certificate]

Abstract

Alzheimer’s disease (AD) is a complex neurodegenerative disorder that involves progressive memory loss and brain atrophy due to deregulated neurobiological networks. Despite decades of intense research, therapies for AD are still in development, and the results of several ongoing pivotal clinical trials are anticipated. Because many recent amyloid-β (Aβ)-targeting therapies have failed, the amyloid hypothesis and alternative clinical strategies need to be reinvestigated. In addition to Aβ inhibition, the inhibition of the hyper-phosphorylation of tau, which is a downstream target of kinases and signaling cascades, is a potential therapeutic strategy. In this review, we discuss current AD treatment strategies that utilize small-molecule therapies that aim to inhibit Aβ accumulation or tau phosphorylation. We then present a comprehensive and balanced overview of recently discovered immunological pathways that make this disease more complex. Targeting these potential pathways will shape future therapeutic approaches in AD.

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Emerging therapeutics and future insights into the pathobiology of Alzheimer’s disease

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Irfan Ullah, Sang-Kyung Lee.
Emerging therapeutics and future insights into the pathobiology of Alzheimer’s disease.
Int. J. Biosci. 12(2), 232-247, February 2018.
https://innspub.net/ijb/emerging-therapeutics-future-insights-pathobiology-alzheimers-disease/
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