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Cardiac Autonomic Regulation and Repolarization During Acute Experimental Hypoglycemia in Type 2 Diabetes

Hypoglycemia is associated with increased cardiovascular mortality in trials of intensive therapy in type 2 diabetes mellitus (T2DM). We previously observed an increase in arrhythmias during spontaneous prolonged hypoglycemia in patients with T2DM. We examined changes in cardiac autonomic function a...

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Autores principales: Chow, Elaine, Bernjak, Alan, Walkinshaw, Emma, Lubina-Solomon, Alexandra, Freeman, Jenny, Macdonald, Ian A., Sheridan, Paul J., Heller, Simon R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5860266/
https://www.ncbi.nlm.nih.gov/pubmed/28137792
http://dx.doi.org/10.2337/db16-1310
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author Chow, Elaine
Bernjak, Alan
Walkinshaw, Emma
Lubina-Solomon, Alexandra
Freeman, Jenny
Macdonald, Ian A.
Sheridan, Paul J.
Heller, Simon R.
author_facet Chow, Elaine
Bernjak, Alan
Walkinshaw, Emma
Lubina-Solomon, Alexandra
Freeman, Jenny
Macdonald, Ian A.
Sheridan, Paul J.
Heller, Simon R.
author_sort Chow, Elaine
collection PubMed
description Hypoglycemia is associated with increased cardiovascular mortality in trials of intensive therapy in type 2 diabetes mellitus (T2DM). We previously observed an increase in arrhythmias during spontaneous prolonged hypoglycemia in patients with T2DM. We examined changes in cardiac autonomic function and repolarization during sustained experimental hypoglycemia. Twelve adults with T2DM and 11 age- and BMI-matched control participants without diabetes underwent paired hyperinsulinemic clamps separated by 4 weeks. Glucose was maintained at euglycemia (6.0 mmol/L) or hypoglycemia (2.5 mmol/L) for 1 h. Heart rate, blood pressure, and heart rate variability were assessed every 30 min and corrected QT intervals and T-wave morphology every 60 min. Heart rate initially increased in participants with T2DM but then fell toward baseline despite maintained hypoglycemia at 1 h accompanied by reactivation of vagal tone. In control participants, vagal tone remained depressed during sustained hypoglycemia. Participants with T2DM exhibited greater heterogeneity of repolarization during hypoglycemia as demonstrated by T-wave symmetry and principal component analysis ratio compared with control participants. Epinephrine levels during hypoglycemia were similar between groups. Cardiac autonomic regulation during hypoglycemia appears to be time dependent. Individuals with T2DM demonstrate greater repolarization abnormalities for a given hypoglycemic stimulus despite comparable sympathoadrenal responses. These mechanisms could contribute to arrhythmias during clinical hypoglycemic episodes.
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spelling pubmed-58602662018-05-01 Cardiac Autonomic Regulation and Repolarization During Acute Experimental Hypoglycemia in Type 2 Diabetes Chow, Elaine Bernjak, Alan Walkinshaw, Emma Lubina-Solomon, Alexandra Freeman, Jenny Macdonald, Ian A. Sheridan, Paul J. Heller, Simon R. Diabetes Pathophysiology Hypoglycemia is associated with increased cardiovascular mortality in trials of intensive therapy in type 2 diabetes mellitus (T2DM). We previously observed an increase in arrhythmias during spontaneous prolonged hypoglycemia in patients with T2DM. We examined changes in cardiac autonomic function and repolarization during sustained experimental hypoglycemia. Twelve adults with T2DM and 11 age- and BMI-matched control participants without diabetes underwent paired hyperinsulinemic clamps separated by 4 weeks. Glucose was maintained at euglycemia (6.0 mmol/L) or hypoglycemia (2.5 mmol/L) for 1 h. Heart rate, blood pressure, and heart rate variability were assessed every 30 min and corrected QT intervals and T-wave morphology every 60 min. Heart rate initially increased in participants with T2DM but then fell toward baseline despite maintained hypoglycemia at 1 h accompanied by reactivation of vagal tone. In control participants, vagal tone remained depressed during sustained hypoglycemia. Participants with T2DM exhibited greater heterogeneity of repolarization during hypoglycemia as demonstrated by T-wave symmetry and principal component analysis ratio compared with control participants. Epinephrine levels during hypoglycemia were similar between groups. Cardiac autonomic regulation during hypoglycemia appears to be time dependent. Individuals with T2DM demonstrate greater repolarization abnormalities for a given hypoglycemic stimulus despite comparable sympathoadrenal responses. These mechanisms could contribute to arrhythmias during clinical hypoglycemic episodes. American Diabetes Association 2017-05 2017-01-30 /pmc/articles/PMC5860266/ /pubmed/28137792 http://dx.doi.org/10.2337/db16-1310 Text en © 2017 by the American Diabetes Association. http://www.diabetesjournals.org/content/licenseReaders 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. More information is available at http://www.diabetesjournals.org/content/license.
spellingShingle Pathophysiology
Chow, Elaine
Bernjak, Alan
Walkinshaw, Emma
Lubina-Solomon, Alexandra
Freeman, Jenny
Macdonald, Ian A.
Sheridan, Paul J.
Heller, Simon R.
Cardiac Autonomic Regulation and Repolarization During Acute Experimental Hypoglycemia in Type 2 Diabetes
title Cardiac Autonomic Regulation and Repolarization During Acute Experimental Hypoglycemia in Type 2 Diabetes
title_full Cardiac Autonomic Regulation and Repolarization During Acute Experimental Hypoglycemia in Type 2 Diabetes
title_fullStr Cardiac Autonomic Regulation and Repolarization During Acute Experimental Hypoglycemia in Type 2 Diabetes
title_full_unstemmed Cardiac Autonomic Regulation and Repolarization During Acute Experimental Hypoglycemia in Type 2 Diabetes
title_short Cardiac Autonomic Regulation and Repolarization During Acute Experimental Hypoglycemia in Type 2 Diabetes
title_sort cardiac autonomic regulation and repolarization during acute experimental hypoglycemia in type 2 diabetes
topic Pathophysiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5860266/
https://www.ncbi.nlm.nih.gov/pubmed/28137792
http://dx.doi.org/10.2337/db16-1310
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