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Impact of Major Depressive Disorder on Prediabetes by Impairing Insulin Sensitivity

Reports regarding the associations between major depressive disorder (MDD) and diabetes remain heterogeneous. Our aim was to investigate whether glucose homeostasis and insulin sensitivity were impaired in the MDD patients and its mechanisms. A total of 30 patients with MDD and 30 matched controls w...

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Autores principales: Li, Li, Shelton, Richard Charles, Chassan, Rachel Ann, Hammond, John Charles, Gower, Barbara Ann, Garvey, Timothy W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892179/
https://www.ncbi.nlm.nih.gov/pubmed/27274905
http://dx.doi.org/10.4172/2155-6156.1000664
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author Li, Li
Shelton, Richard Charles
Chassan, Rachel Ann
Hammond, John Charles
Gower, Barbara Ann
Garvey, Timothy W
author_facet Li, Li
Shelton, Richard Charles
Chassan, Rachel Ann
Hammond, John Charles
Gower, Barbara Ann
Garvey, Timothy W
author_sort Li, Li
collection PubMed
description Reports regarding the associations between major depressive disorder (MDD) and diabetes remain heterogeneous. Our aim was to investigate whether glucose homeostasis and insulin sensitivity were impaired in the MDD patients and its mechanisms. A total of 30 patients with MDD and 30 matched controls were recruited. The oral glucose tolerance test and dual-energy X-ray absorptiometry scan were performed in each participant. Insulin signaling in postmortem brain tissues from other depressive patients and controls (obtained from Alabama brain bank) was examined. Insulin sensitivity was reduced substantially in the MDD patients, however, the fasting and 2-h glucose concentrations remained within the normal range through compensatory insulin secretion. Despite increased insulin secretion, 1-h glucose concentrations in the MDD patients were significantly elevated compared with the controls. MDD patients had greater visceral fat mass but lower adiponectin levels compared with the controls. Furthermore, phosphorylated-AKT levels in insulin signaling were decreased in postmortem brain tissues in patients with MDD. These results suggest that MDD patients are at a greater risk for diabetes due to decreased insulin sensitivity, reduced disposition index, and impaired glucose tolerance as manifested by elevated 1-h glucose concentrations following an oral glucose challenge. Mechanistic studies reveal that decreased insulin sensitivity is associated with increased visceral fat mass, lower adiponectin levels and impaired insulin action in postmortem brain tissues in the MDD patients. Our findings emphasize the importance of screening depressive patients to identify susceptible individuals for developing future diabetes with the hope of improving their health outcomes.
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spelling pubmed-48921792016-06-03 Impact of Major Depressive Disorder on Prediabetes by Impairing Insulin Sensitivity Li, Li Shelton, Richard Charles Chassan, Rachel Ann Hammond, John Charles Gower, Barbara Ann Garvey, Timothy W J Diabetes Metab Article Reports regarding the associations between major depressive disorder (MDD) and diabetes remain heterogeneous. Our aim was to investigate whether glucose homeostasis and insulin sensitivity were impaired in the MDD patients and its mechanisms. A total of 30 patients with MDD and 30 matched controls were recruited. The oral glucose tolerance test and dual-energy X-ray absorptiometry scan were performed in each participant. Insulin signaling in postmortem brain tissues from other depressive patients and controls (obtained from Alabama brain bank) was examined. Insulin sensitivity was reduced substantially in the MDD patients, however, the fasting and 2-h glucose concentrations remained within the normal range through compensatory insulin secretion. Despite increased insulin secretion, 1-h glucose concentrations in the MDD patients were significantly elevated compared with the controls. MDD patients had greater visceral fat mass but lower adiponectin levels compared with the controls. Furthermore, phosphorylated-AKT levels in insulin signaling were decreased in postmortem brain tissues in patients with MDD. These results suggest that MDD patients are at a greater risk for diabetes due to decreased insulin sensitivity, reduced disposition index, and impaired glucose tolerance as manifested by elevated 1-h glucose concentrations following an oral glucose challenge. Mechanistic studies reveal that decreased insulin sensitivity is associated with increased visceral fat mass, lower adiponectin levels and impaired insulin action in postmortem brain tissues in the MDD patients. Our findings emphasize the importance of screening depressive patients to identify susceptible individuals for developing future diabetes with the hope of improving their health outcomes. 2016-04-28 2016-04 /pmc/articles/PMC4892179/ /pubmed/27274905 http://dx.doi.org/10.4172/2155-6156.1000664 Text en http://creativecommons.org/licenses/by/2.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Li, Li
Shelton, Richard Charles
Chassan, Rachel Ann
Hammond, John Charles
Gower, Barbara Ann
Garvey, Timothy W
Impact of Major Depressive Disorder on Prediabetes by Impairing Insulin Sensitivity
title Impact of Major Depressive Disorder on Prediabetes by Impairing Insulin Sensitivity
title_full Impact of Major Depressive Disorder on Prediabetes by Impairing Insulin Sensitivity
title_fullStr Impact of Major Depressive Disorder on Prediabetes by Impairing Insulin Sensitivity
title_full_unstemmed Impact of Major Depressive Disorder on Prediabetes by Impairing Insulin Sensitivity
title_short Impact of Major Depressive Disorder on Prediabetes by Impairing Insulin Sensitivity
title_sort impact of major depressive disorder on prediabetes by impairing insulin sensitivity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892179/
https://www.ncbi.nlm.nih.gov/pubmed/27274905
http://dx.doi.org/10.4172/2155-6156.1000664
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