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Brain Activation During Working Memory Is Altered in Patients With Type 1 Diabetes During Hypoglycemia

OBJECTIVE: To investigate the effects of acute hypoglycemia on working memory and brain function in patients with type 1 diabetes. RESEARCH DESIGN AND METHODS: Using blood oxygen level–dependent (BOLD) functional magnetic resonance imaging during euglycemic (5.0 mmol/L) and hypoglycemic (2.8 mmol/L)...

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Autores principales: Bolo, Nicolas R., Musen, Gail, Jacobson, Alan M., Weinger, Katie, McCartney, Richard L., Flores, Veronica, Renshaw, Perry F., Simonson, Donald C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219930/
https://www.ncbi.nlm.nih.gov/pubmed/21984582
http://dx.doi.org/10.2337/db11-0506
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author Bolo, Nicolas R.
Musen, Gail
Jacobson, Alan M.
Weinger, Katie
McCartney, Richard L.
Flores, Veronica
Renshaw, Perry F.
Simonson, Donald C.
author_facet Bolo, Nicolas R.
Musen, Gail
Jacobson, Alan M.
Weinger, Katie
McCartney, Richard L.
Flores, Veronica
Renshaw, Perry F.
Simonson, Donald C.
author_sort Bolo, Nicolas R.
collection PubMed
description OBJECTIVE: To investigate the effects of acute hypoglycemia on working memory and brain function in patients with type 1 diabetes. RESEARCH DESIGN AND METHODS: Using blood oxygen level–dependent (BOLD) functional magnetic resonance imaging during euglycemic (5.0 mmol/L) and hypoglycemic (2.8 mmol/L) hyperinsulinemic clamps, we compared brain activation response to a working-memory task (WMT) in type 1 diabetic subjects (n = 16) with that in age-matched nondiabetic control subjects (n = 16). Behavioral performance was assessed by percent correct responses. RESULTS: During euglycemia, the WMT activated the bilateral frontal and parietal cortices, insula, thalamus, and cerebellum in both groups. During hypoglycemia, activation decreased in both groups but remained 80% larger in type 1 diabetic versus control subjects (P < 0.05). In type 1 diabetic subjects, higher HbA(1c) was associated with lower activation in the right parahippocampal gyrus and amygdala (R(2) = 0.45, P < 0.002). Deactivation of the default-mode network (DMN) also was seen in both groups during euglycemia. However, during hypoglycemia, type 1 diabetic patients deactivated the DMN 70% less than control subjects (P < 0.05). Behavioral performance did not differ between glycemic conditions or groups. CONCLUSIONS: BOLD activation was increased and deactivation was decreased in type 1 diabetic versus control subjects during hypoglycemia. This higher level of brain activation required by type 1 diabetic subjects to attain the same level of cognitive performance as control subjects suggests reduced cerebral efficiency in type 1 diabetes.
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spelling pubmed-32199302012-12-01 Brain Activation During Working Memory Is Altered in Patients With Type 1 Diabetes During Hypoglycemia Bolo, Nicolas R. Musen, Gail Jacobson, Alan M. Weinger, Katie McCartney, Richard L. Flores, Veronica Renshaw, Perry F. Simonson, Donald C. Diabetes Complications OBJECTIVE: To investigate the effects of acute hypoglycemia on working memory and brain function in patients with type 1 diabetes. RESEARCH DESIGN AND METHODS: Using blood oxygen level–dependent (BOLD) functional magnetic resonance imaging during euglycemic (5.0 mmol/L) and hypoglycemic (2.8 mmol/L) hyperinsulinemic clamps, we compared brain activation response to a working-memory task (WMT) in type 1 diabetic subjects (n = 16) with that in age-matched nondiabetic control subjects (n = 16). Behavioral performance was assessed by percent correct responses. RESULTS: During euglycemia, the WMT activated the bilateral frontal and parietal cortices, insula, thalamus, and cerebellum in both groups. During hypoglycemia, activation decreased in both groups but remained 80% larger in type 1 diabetic versus control subjects (P < 0.05). In type 1 diabetic subjects, higher HbA(1c) was associated with lower activation in the right parahippocampal gyrus and amygdala (R(2) = 0.45, P < 0.002). Deactivation of the default-mode network (DMN) also was seen in both groups during euglycemia. However, during hypoglycemia, type 1 diabetic patients deactivated the DMN 70% less than control subjects (P < 0.05). Behavioral performance did not differ between glycemic conditions or groups. CONCLUSIONS: BOLD activation was increased and deactivation was decreased in type 1 diabetic versus control subjects during hypoglycemia. This higher level of brain activation required by type 1 diabetic subjects to attain the same level of cognitive performance as control subjects suggests reduced cerebral efficiency in type 1 diabetes. American Diabetes Association 2011-12 2011-11-13 /pmc/articles/PMC3219930/ /pubmed/21984582 http://dx.doi.org/10.2337/db11-0506 Text en © 2011 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. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Complications
Bolo, Nicolas R.
Musen, Gail
Jacobson, Alan M.
Weinger, Katie
McCartney, Richard L.
Flores, Veronica
Renshaw, Perry F.
Simonson, Donald C.
Brain Activation During Working Memory Is Altered in Patients With Type 1 Diabetes During Hypoglycemia
title Brain Activation During Working Memory Is Altered in Patients With Type 1 Diabetes During Hypoglycemia
title_full Brain Activation During Working Memory Is Altered in Patients With Type 1 Diabetes During Hypoglycemia
title_fullStr Brain Activation During Working Memory Is Altered in Patients With Type 1 Diabetes During Hypoglycemia
title_full_unstemmed Brain Activation During Working Memory Is Altered in Patients With Type 1 Diabetes During Hypoglycemia
title_short Brain Activation During Working Memory Is Altered in Patients With Type 1 Diabetes During Hypoglycemia
title_sort brain activation during working memory is altered in patients with type 1 diabetes during hypoglycemia
topic Complications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219930/
https://www.ncbi.nlm.nih.gov/pubmed/21984582
http://dx.doi.org/10.2337/db11-0506
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