Insulin as a Bridge between Type 2 Diabetes and Alzheimer Disease - How Anti-Diabetics Could be a Solution for Dementia.

Front Endocrinol (Lausanne)

Center for Neuroscience and Cell Biology (CNC), University of Coimbra, Coimbra , Portugal ; Institute for Interdisciplinary Research (IIIUC), University of Coimbra, Coimbra , Portugal.

Published: July 2014

AI Article Synopsis

  • Type 2 diabetes (T2D) and Alzheimer’s disease (AD) are interconnected health issues, with T2D affecting millions of elderly individuals and increasing the risk for AD due to shared complications.
  • Research suggests that insulin resistance, a key feature of T2D, also occurs in AD, leading to the classification of AD as "type 3 diabetes" and indicating that treatments for T2D could benefit AD patients.
  • The review focuses on the overlap in insulin signaling related to the formation of amyloid plaques and neurofibrillary tangles in AD, and discusses the potential of certain anti-T2D medications, especially GLP-1 receptor agonists, to protect against cognitive decline and dementia.

Article Abstract

Type 2 diabetes (T2D) and Alzheimer disease (AD) are two major health issues nowadays. T2D is an ever increasing epidemic, affecting millions of elderly people worldwide, with major repercussions in the patients' daily life. This is mostly due to its chronic complications that may affect brain and constitutes a risk factor for AD. T2D principal hallmark is insulin resistance which also occurs in AD, rendering both pathologies more than mere unrelated diseases. This hypothesis has been reinforced in the recent years, with a high number of studies highlighting the existence of several common molecular links. As such, it is not surprising that AD has been considered as the "type 3 diabetes" or a "brain-specific T2D," supporting the idea that a beneficial therapeutic strategy against T2D might be also beneficial against AD. Herewith, we aim to review some of the recent developments on the common features between T2D and AD, namely on insulin signaling and its participation in the regulation of amyloid β (Aβ) plaque and neurofibrillary tangle formation (the two major neuropathological hallmarks of AD). We also critically analyze the promising field that some anti-T2D drugs may protect against dementia and AD, with a special emphasis on the novel incretin/glucagon-like peptide-1 receptor agonists.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086025PMC
http://dx.doi.org/10.3389/fendo.2014.00110DOI Listing

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