Sex differences in brain functional connectivity of hippocampus in mild cognitive impairment

Mild cognitive impairment (MCI) is the prodromal stage of Alzheimer’s Disease (AD). Prior research shows that females are more impacted by MCI than males. On average females have a greater incidence rate of any dementia and current evidence suggests that they suffer greater cognitive deterioration t...

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Main Authors: Jordan Williamson, Andriy Yabluchanskiy, Peter Mukli, Dee H. Wu, William Sonntag, Carrie Ciro, Yuan Yang
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-08-01
Series:Frontiers in Aging Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnagi.2022.959394/full
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author Jordan Williamson
Andriy Yabluchanskiy
Peter Mukli
Dee H. Wu
Dee H. Wu
Dee H. Wu
Dee H. Wu
William Sonntag
Carrie Ciro
Yuan Yang
Yuan Yang
Yuan Yang
Yuan Yang
Yuan Yang
author_facet Jordan Williamson
Andriy Yabluchanskiy
Peter Mukli
Dee H. Wu
Dee H. Wu
Dee H. Wu
Dee H. Wu
William Sonntag
Carrie Ciro
Yuan Yang
Yuan Yang
Yuan Yang
Yuan Yang
Yuan Yang
author_sort Jordan Williamson
collection DOAJ
description Mild cognitive impairment (MCI) is the prodromal stage of Alzheimer’s Disease (AD). Prior research shows that females are more impacted by MCI than males. On average females have a greater incidence rate of any dementia and current evidence suggests that they suffer greater cognitive deterioration than males in the same disease stage. Recent research has linked these sex differences to neuroimaging markers of brain pathology, such as hippocampal volumes. Specifically, the rate of hippocampal atrophy affects the progression of AD in females more than males. This study was designed to extend our understanding of the sex-related differences in the brain of participants with MCI. Specifically, we investigated the difference in the hippocampal connectivity to different areas of the brain. The Resting State fMRI and T2 MRI of cognitively normal individuals (n = 40, female = 20) and individuals with MCI (n = 40, female = 20) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) were analyzed using the Functional Connectivity Toolbox (CONN). Our results demonstrate that connectivity of hippocampus to the precuneus cortex and brain stem was significantly stronger in males than in females. These results improve our current understanding of the role of hippocampus-precuneus cortex and hippocampus-brainstem connectivity in sex differences in MCI. Understanding the contribution of impaired functional connectivity sex differences may aid in the development of sex specific precision medicine to manipulate hippocampal-precuneus cortex and hippocampal-brainstem connectivity to decrease the progression of MCI to AD.
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spelling doaj.art-71efcb3a39994c19812a6b9e7e47e5612022-12-22T02:34:10ZengFrontiers Media S.A.Frontiers in Aging Neuroscience1663-43652022-08-011410.3389/fnagi.2022.959394959394Sex differences in brain functional connectivity of hippocampus in mild cognitive impairmentJordan Williamson0Andriy Yabluchanskiy1Peter Mukli2Dee H. Wu3Dee H. Wu4Dee H. Wu5Dee H. Wu6William Sonntag7Carrie Ciro8Yuan Yang9Yuan Yang10Yuan Yang11Yuan Yang12Yuan Yang13Neural Control and Rehabilitation Laboratory, Stephenson School of Biomedical Engineering, University of Oklahoma, Norman, OK, United StatesVascular Cognitive Impairment and Neurodegeneration Program, Oklahoma Center for Geroscience and Healthy Brain Aging, Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United StatesVascular Cognitive Impairment and Neurodegeneration Program, Oklahoma Center for Geroscience and Healthy Brain Aging, Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United StatesDepartment of Radiological Science and Medical Physics, University of Oklahoma Health Science Center, Oklahoma City, OK, United StatesData Institute for Societal Challenges, University of Oklahoma, Norman, OK, United StatesSchool of Computer Science, Gallogly College of Engineering, University of Oklahoma, Norman, OK, United StatesSchool of Electrical and Computer Engineering, Gallogly College of Engineering, University of Oklahoma, Norman, OK, United StatesVascular Cognitive Impairment and Neurodegeneration Program, Oklahoma Center for Geroscience and Healthy Brain Aging, Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United StatesDepartment of Rehabilitation Sciences, University of Oklahoma Health Science Center, Oklahoma City, OK, United StatesNeural Control and Rehabilitation Laboratory, Stephenson School of Biomedical Engineering, University of Oklahoma, Norman, OK, United StatesData Institute for Societal Challenges, University of Oklahoma, Norman, OK, United StatesDepartment of Rehabilitation Sciences, University of Oklahoma Health Science Center, Oklahoma City, OK, United StatesSchool of Electrical and Computer Engineering, University of Oklahoma, Tulsa, OK, United StatesDepartment of Physical Therapy and Human Movement Sciences, Northwestern University, Chicago, IL, United StatesMild cognitive impairment (MCI) is the prodromal stage of Alzheimer’s Disease (AD). Prior research shows that females are more impacted by MCI than males. On average females have a greater incidence rate of any dementia and current evidence suggests that they suffer greater cognitive deterioration than males in the same disease stage. Recent research has linked these sex differences to neuroimaging markers of brain pathology, such as hippocampal volumes. Specifically, the rate of hippocampal atrophy affects the progression of AD in females more than males. This study was designed to extend our understanding of the sex-related differences in the brain of participants with MCI. Specifically, we investigated the difference in the hippocampal connectivity to different areas of the brain. The Resting State fMRI and T2 MRI of cognitively normal individuals (n = 40, female = 20) and individuals with MCI (n = 40, female = 20) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) were analyzed using the Functional Connectivity Toolbox (CONN). Our results demonstrate that connectivity of hippocampus to the precuneus cortex and brain stem was significantly stronger in males than in females. These results improve our current understanding of the role of hippocampus-precuneus cortex and hippocampus-brainstem connectivity in sex differences in MCI. Understanding the contribution of impaired functional connectivity sex differences may aid in the development of sex specific precision medicine to manipulate hippocampal-precuneus cortex and hippocampal-brainstem connectivity to decrease the progression of MCI to AD.https://www.frontiersin.org/articles/10.3389/fnagi.2022.959394/fullmild cognitive impairmentsex differencehippocampusfunctional connectivityAlzheimer’s disease
spellingShingle Jordan Williamson
Andriy Yabluchanskiy
Peter Mukli
Dee H. Wu
Dee H. Wu
Dee H. Wu
Dee H. Wu
William Sonntag
Carrie Ciro
Yuan Yang
Yuan Yang
Yuan Yang
Yuan Yang
Yuan Yang
Sex differences in brain functional connectivity of hippocampus in mild cognitive impairment
Frontiers in Aging Neuroscience
mild cognitive impairment
sex difference
hippocampus
functional connectivity
Alzheimer’s disease
title Sex differences in brain functional connectivity of hippocampus in mild cognitive impairment
title_full Sex differences in brain functional connectivity of hippocampus in mild cognitive impairment
title_fullStr Sex differences in brain functional connectivity of hippocampus in mild cognitive impairment
title_full_unstemmed Sex differences in brain functional connectivity of hippocampus in mild cognitive impairment
title_short Sex differences in brain functional connectivity of hippocampus in mild cognitive impairment
title_sort sex differences in brain functional connectivity of hippocampus in mild cognitive impairment
topic mild cognitive impairment
sex difference
hippocampus
functional connectivity
Alzheimer’s disease
url https://www.frontiersin.org/articles/10.3389/fnagi.2022.959394/full
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