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Task-Induced Brain Activity Patterns in Type 2 Diabetes: A Potential Biomarker for Cognitive Decline
Patients with type 2 diabetes demonstrate reduced functional connectivity within the resting state default mode network (DMN), which may signal heightened risk for cognitive decline. In other populations at risk for cognitive decline, additional magnetic resonance imaging abnormalities are evident d...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141362/ https://www.ncbi.nlm.nih.gov/pubmed/24705405 http://dx.doi.org/10.2337/db13-1783 |
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author | Marder, Thomas J. Flores, Veronica L. Bolo, Nicolas R. Hoogenboom, Wouter S. Simonson, Donald C. Jacobson, Alan M. Foote, Sarah E. Shenton, Martha E. Sperling, Reisa A. Musen, Gail |
author_facet | Marder, Thomas J. Flores, Veronica L. Bolo, Nicolas R. Hoogenboom, Wouter S. Simonson, Donald C. Jacobson, Alan M. Foote, Sarah E. Shenton, Martha E. Sperling, Reisa A. Musen, Gail |
author_sort | Marder, Thomas J. |
collection | PubMed |
description | Patients with type 2 diabetes demonstrate reduced functional connectivity within the resting state default mode network (DMN), which may signal heightened risk for cognitive decline. In other populations at risk for cognitive decline, additional magnetic resonance imaging abnormalities are evident during task performance, including impaired deactivation of the DMN and reduced activation of task-relevant regions. We investigated whether middle-aged type 2 diabetic patients show these brain activity patterns during encoding and recognition tasks. Compared with control participants, we observed both reduced 1) activation of the dorsolateral prefrontal cortex during encoding and 2) deactivation of the DMN during recognition in type 2 diabetic patients, despite normal cognition. During recognition, activation in several task-relevant regions, including the dorsolateral prefrontal cortex and DMN regions, was positively correlated with HbA(1c) and insulin resistance, suggesting that these important markers of glucose metabolism impact the brain’s response to a cognitive challenge. Plasma glucose ≥11 mmol/L was associated with impaired deactivation of the DMN, suggesting that acute hyperglycemia contributes to brain abnormalities. Since elderly type 2 diabetic patients often demonstrate cognitive impairments, it is possible that these task-induced brain activity patterns observed in middle age may signal impending cognitive decline. |
format | Online Article Text |
id | pubmed-4141362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-41413622015-09-01 Task-Induced Brain Activity Patterns in Type 2 Diabetes: A Potential Biomarker for Cognitive Decline Marder, Thomas J. Flores, Veronica L. Bolo, Nicolas R. Hoogenboom, Wouter S. Simonson, Donald C. Jacobson, Alan M. Foote, Sarah E. Shenton, Martha E. Sperling, Reisa A. Musen, Gail Diabetes Complications Patients with type 2 diabetes demonstrate reduced functional connectivity within the resting state default mode network (DMN), which may signal heightened risk for cognitive decline. In other populations at risk for cognitive decline, additional magnetic resonance imaging abnormalities are evident during task performance, including impaired deactivation of the DMN and reduced activation of task-relevant regions. We investigated whether middle-aged type 2 diabetic patients show these brain activity patterns during encoding and recognition tasks. Compared with control participants, we observed both reduced 1) activation of the dorsolateral prefrontal cortex during encoding and 2) deactivation of the DMN during recognition in type 2 diabetic patients, despite normal cognition. During recognition, activation in several task-relevant regions, including the dorsolateral prefrontal cortex and DMN regions, was positively correlated with HbA(1c) and insulin resistance, suggesting that these important markers of glucose metabolism impact the brain’s response to a cognitive challenge. Plasma glucose ≥11 mmol/L was associated with impaired deactivation of the DMN, suggesting that acute hyperglycemia contributes to brain abnormalities. Since elderly type 2 diabetic patients often demonstrate cognitive impairments, it is possible that these task-induced brain activity patterns observed in middle age may signal impending cognitive decline. American Diabetes Association 2014-09 2014-08-16 /pmc/articles/PMC4141362/ /pubmed/24705405 http://dx.doi.org/10.2337/db13-1783 Text en © 2014 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. |
spellingShingle | Complications Marder, Thomas J. Flores, Veronica L. Bolo, Nicolas R. Hoogenboom, Wouter S. Simonson, Donald C. Jacobson, Alan M. Foote, Sarah E. Shenton, Martha E. Sperling, Reisa A. Musen, Gail Task-Induced Brain Activity Patterns in Type 2 Diabetes: A Potential Biomarker for Cognitive Decline |
title | Task-Induced Brain Activity Patterns in Type 2 Diabetes: A Potential Biomarker for Cognitive Decline |
title_full | Task-Induced Brain Activity Patterns in Type 2 Diabetes: A Potential Biomarker for Cognitive Decline |
title_fullStr | Task-Induced Brain Activity Patterns in Type 2 Diabetes: A Potential Biomarker for Cognitive Decline |
title_full_unstemmed | Task-Induced Brain Activity Patterns in Type 2 Diabetes: A Potential Biomarker for Cognitive Decline |
title_short | Task-Induced Brain Activity Patterns in Type 2 Diabetes: A Potential Biomarker for Cognitive Decline |
title_sort | task-induced brain activity patterns in type 2 diabetes: a potential biomarker for cognitive decline |
topic | Complications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141362/ https://www.ncbi.nlm.nih.gov/pubmed/24705405 http://dx.doi.org/10.2337/db13-1783 |
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