Repurposing Diabetes Drugs for Brain Insulin Resistance in Alzheimer Disease

A growing body of clinical and epidemiological research suggests that two of the most common diseases of aging, type 2 diabetes (T2DM) and Alzheimer disease (AD), are linked. The nature of the association is not known, but this observation has led to the notion that drugs developed for the treatment...

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Main Authors: Yarchoan, Mark, Arnold, Steven E.
Format: Online
Language:English
Published: American Diabetes Association 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066335/
id pubmed-4066335
recordtype oai_dc
spelling pubmed-40663352015-07-01 Repurposing Diabetes Drugs for Brain Insulin Resistance in Alzheimer Disease Yarchoan, Mark Arnold, Steven E. Diabetes Symposium: Dementia and Diabetes A growing body of clinical and epidemiological research suggests that two of the most common diseases of aging, type 2 diabetes (T2DM) and Alzheimer disease (AD), are linked. The nature of the association is not known, but this observation has led to the notion that drugs developed for the treatment of T2DM may be beneficial in modifying the pathophysiology of AD and maintaining cognitive function. Recent advances in the understanding of the biology of T2DM have resulted in a growing number of therapies that are approved or in clinical development for this disease. This review summarizes the evidence that T2DM and AD are linked, with a focus on the cellular and molecular mechanisms in common, and then assesses the various clinical-stage diabetes drugs for their potential activity in AD. At a time when existing therapies for AD offer only limited symptomatic benefit for some patients, additional clinical trials of diabetes drugs are needed to at least advance the care of T2DM patients at risk for or with comorbid AD and also to determine their value for AD in general. American Diabetes Association 2014-07 2014-06-14 /pmc/articles/PMC4066335/ /pubmed/24931035 http://dx.doi.org/10.2337/db14-0287 Text en © 2014 by the American Diabetes Association. Readers may use the content as long as the work is properly cited and linked to the original source, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Yarchoan, Mark
Arnold, Steven E.
spellingShingle Yarchoan, Mark
Arnold, Steven E.
Repurposing Diabetes Drugs for Brain Insulin Resistance in Alzheimer Disease
author_facet Yarchoan, Mark
Arnold, Steven E.
author_sort Yarchoan, Mark
title Repurposing Diabetes Drugs for Brain Insulin Resistance in Alzheimer Disease
title_short Repurposing Diabetes Drugs for Brain Insulin Resistance in Alzheimer Disease
title_full Repurposing Diabetes Drugs for Brain Insulin Resistance in Alzheimer Disease
title_fullStr Repurposing Diabetes Drugs for Brain Insulin Resistance in Alzheimer Disease
title_full_unstemmed Repurposing Diabetes Drugs for Brain Insulin Resistance in Alzheimer Disease
title_sort repurposing diabetes drugs for brain insulin resistance in alzheimer disease
description A growing body of clinical and epidemiological research suggests that two of the most common diseases of aging, type 2 diabetes (T2DM) and Alzheimer disease (AD), are linked. The nature of the association is not known, but this observation has led to the notion that drugs developed for the treatment of T2DM may be beneficial in modifying the pathophysiology of AD and maintaining cognitive function. Recent advances in the understanding of the biology of T2DM have resulted in a growing number of therapies that are approved or in clinical development for this disease. This review summarizes the evidence that T2DM and AD are linked, with a focus on the cellular and molecular mechanisms in common, and then assesses the various clinical-stage diabetes drugs for their potential activity in AD. At a time when existing therapies for AD offer only limited symptomatic benefit for some patients, additional clinical trials of diabetes drugs are needed to at least advance the care of T2DM patients at risk for or with comorbid AD and also to determine their value for AD in general.
publisher American Diabetes Association
publishDate 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066335/
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