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The Abnormal Functional Connectivity between the Hypothalamus and the Temporal Gyrus Underlying Depression in Alzheimer’s Disease Patients

Hypothalamic communication with the rest of the brain is critical for accomplishing a wide variety of physiological and psychological functions, including the maintenance of neuroendocrine circadian rhythms and the management of affective processes. Evidence has shown that major depressive disorder...

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Autores principales: Liu, Xiaozheng, Chen, Wei, Tu, Yunhai, Hou, Hongtao, Huang, Xiaoyan, Chen, Xingli, Guo, Zhongwei, Bai, Guanghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816744/
https://www.ncbi.nlm.nih.gov/pubmed/29487521
http://dx.doi.org/10.3389/fnagi.2018.00037
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author Liu, Xiaozheng
Chen, Wei
Tu, Yunhai
Hou, Hongtao
Huang, Xiaoyan
Chen, Xingli
Guo, Zhongwei
Bai, Guanghui
Chen, Wei
author_facet Liu, Xiaozheng
Chen, Wei
Tu, Yunhai
Hou, Hongtao
Huang, Xiaoyan
Chen, Xingli
Guo, Zhongwei
Bai, Guanghui
Chen, Wei
author_sort Liu, Xiaozheng
collection PubMed
description Hypothalamic communication with the rest of the brain is critical for accomplishing a wide variety of physiological and psychological functions, including the maintenance of neuroendocrine circadian rhythms and the management of affective processes. Evidence has shown that major depressive disorder (MDD) patients exhibit increased functioning of the hypothalamic-pituitary-adrenal (HPA) axis. Neurofibrillary tangles are also found in the hypothalamus of Alzheimer’s disease (AD) patients, and AD patients exhibit abnormal changes in the HPA. However, little is known of how the hypothalamus interacts with other brain regions in AD patients with depression (D-AD). Functional connectivity (FC) analysis explores the connectivity between brain regions that share functional properties. Here, we used resting-state (rs) magnetic resonance imaging (MRI) technology and the FC method to measure hypothalamic connectivity across the whole brain in 22 D-AD patients and 21 non-depressed AD patients (nD-AD). Our results showed that D-AD patients had reduced FC among the hypothalamus, the right middle temporal gyrus (MTG) and the right superior temporal gyrus (STG) compared with the FC of nD-AD patients, suggesting that the abnormal FC between the hypothalamus and the temporal lobe may play a key role in the pathophysiology of depression in AD patients.
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spelling pubmed-58167442018-02-27 The Abnormal Functional Connectivity between the Hypothalamus and the Temporal Gyrus Underlying Depression in Alzheimer’s Disease Patients Liu, Xiaozheng Chen, Wei Tu, Yunhai Hou, Hongtao Huang, Xiaoyan Chen, Xingli Guo, Zhongwei Bai, Guanghui Chen, Wei Front Aging Neurosci Neuroscience Hypothalamic communication with the rest of the brain is critical for accomplishing a wide variety of physiological and psychological functions, including the maintenance of neuroendocrine circadian rhythms and the management of affective processes. Evidence has shown that major depressive disorder (MDD) patients exhibit increased functioning of the hypothalamic-pituitary-adrenal (HPA) axis. Neurofibrillary tangles are also found in the hypothalamus of Alzheimer’s disease (AD) patients, and AD patients exhibit abnormal changes in the HPA. However, little is known of how the hypothalamus interacts with other brain regions in AD patients with depression (D-AD). Functional connectivity (FC) analysis explores the connectivity between brain regions that share functional properties. Here, we used resting-state (rs) magnetic resonance imaging (MRI) technology and the FC method to measure hypothalamic connectivity across the whole brain in 22 D-AD patients and 21 non-depressed AD patients (nD-AD). Our results showed that D-AD patients had reduced FC among the hypothalamus, the right middle temporal gyrus (MTG) and the right superior temporal gyrus (STG) compared with the FC of nD-AD patients, suggesting that the abnormal FC between the hypothalamus and the temporal lobe may play a key role in the pathophysiology of depression in AD patients. Frontiers Media S.A. 2018-02-13 /pmc/articles/PMC5816744/ /pubmed/29487521 http://dx.doi.org/10.3389/fnagi.2018.00037 Text en Copyright © 2018 Liu, Chen, Tu, Hou, Huang, Chen, Guo, Bai and Chen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Liu, Xiaozheng
Chen, Wei
Tu, Yunhai
Hou, Hongtao
Huang, Xiaoyan
Chen, Xingli
Guo, Zhongwei
Bai, Guanghui
Chen, Wei
The Abnormal Functional Connectivity between the Hypothalamus and the Temporal Gyrus Underlying Depression in Alzheimer’s Disease Patients
title The Abnormal Functional Connectivity between the Hypothalamus and the Temporal Gyrus Underlying Depression in Alzheimer’s Disease Patients
title_full The Abnormal Functional Connectivity between the Hypothalamus and the Temporal Gyrus Underlying Depression in Alzheimer’s Disease Patients
title_fullStr The Abnormal Functional Connectivity between the Hypothalamus and the Temporal Gyrus Underlying Depression in Alzheimer’s Disease Patients
title_full_unstemmed The Abnormal Functional Connectivity between the Hypothalamus and the Temporal Gyrus Underlying Depression in Alzheimer’s Disease Patients
title_short The Abnormal Functional Connectivity between the Hypothalamus and the Temporal Gyrus Underlying Depression in Alzheimer’s Disease Patients
title_sort abnormal functional connectivity between the hypothalamus and the temporal gyrus underlying depression in alzheimer’s disease patients
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816744/
https://www.ncbi.nlm.nih.gov/pubmed/29487521
http://dx.doi.org/10.3389/fnagi.2018.00037
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