Cargando…

Association of Tau Pathology With Clinical Symptoms in the Subfields of Hippocampal Formation

Objective: To delineate the relationship between clinical symptoms and tauopathy of the hippocampal subfields under different amyloid statuses. Methods: One hundred and forty-three subjects were obtained from the ADNI project, including 87 individuals with normal cognition, 46 with mild cognitive im...

Descripción completa

Detalles Bibliográficos
Autores principales: Ge, Xinting, Zhang, Dan, Qiao, Yuchuan, Zhang, Jiong, Xu, Junhai, Zheng, Yuanjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317580/
https://www.ncbi.nlm.nih.gov/pubmed/34335226
http://dx.doi.org/10.3389/fnagi.2021.672077
_version_ 1783730096278863872
author Ge, Xinting
Zhang, Dan
Qiao, Yuchuan
Zhang, Jiong
Xu, Junhai
Zheng, Yuanjie
author_facet Ge, Xinting
Zhang, Dan
Qiao, Yuchuan
Zhang, Jiong
Xu, Junhai
Zheng, Yuanjie
author_sort Ge, Xinting
collection PubMed
description Objective: To delineate the relationship between clinical symptoms and tauopathy of the hippocampal subfields under different amyloid statuses. Methods: One hundred and forty-three subjects were obtained from the ADNI project, including 87 individuals with normal cognition, 46 with mild cognitive impairment, and 10 with Alzheimer’s disease (AD). All subjects underwent the tau PET, amyloid PET, T1W, and high-resolution T2W scans. Clinical symptoms were assessed by the Neuropsychiatric Inventory (NPI) total score and Alzheimer’s Disease Assessment Scale cognition 13 (ADAS-cog-13) total score, comprising memory and executive function scores. The hippocampal subfields including Cornu Ammonis (CA1–3), subiculum (Sub), and dentate gyrus (DG), as well as the adjacent para-hippocampus (PHC) and entorhinal cortex (ERC), were segmented automatically using the Automatic Segmentation of Hippocampal Subfields (ASHS) software. The relationship between tauopathy/volume of the hippocampal subfields and assessment scores was calculated using partial correlation analysis under different amyloid status, by controlling age, gender, education, apolipoprotein E (APOE) allele ɛ4 carrier status, and, time interval between the acquisition time of tau PET and amyloid PET scans. Results: Compared with amyloid negative (A−) group, individuals from amyloid positive (A+) group are more impaired based on the Mini-mental State Examination (MMSE; p = 3.82e-05), memory (p = 6.30e-04), executive function (p = 0.0016), and ADAS-cog-13 scores (p = 5.11e-04). Significant decrease of volume (CA1, DG, and Sub) and increase of tau deposition (CA1, Sub, ERC, and PHC) of the hippocampal subfields of both hemispheres were observed for the A+ group compared to the A- group. Tauopathy of ERC is significantly associated with memory score for the A- group, and the associated regions spread into Sub and PHC for the A+ group. The relationship between the impairment of behavior or executive function and tauopathy of the hippocampal subfield was discovered within the A+ group. Leftward asymmetry was observed with the association between assessment scores and tauopathy of the hippocampal subfield, which is more prominent for the NPI score for the A+ group. Conclusion: The associations of tauopathy/volume of the hippocampal subfields with clinical symptoms provide additional insight into the understanding of local changes of the human HF during the AD continuum and can be used as a reference for future studies.
format Online
Article
Text
id pubmed-8317580
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-83175802021-07-29 Association of Tau Pathology With Clinical Symptoms in the Subfields of Hippocampal Formation Ge, Xinting Zhang, Dan Qiao, Yuchuan Zhang, Jiong Xu, Junhai Zheng, Yuanjie Front Aging Neurosci Neuroscience Objective: To delineate the relationship between clinical symptoms and tauopathy of the hippocampal subfields under different amyloid statuses. Methods: One hundred and forty-three subjects were obtained from the ADNI project, including 87 individuals with normal cognition, 46 with mild cognitive impairment, and 10 with Alzheimer’s disease (AD). All subjects underwent the tau PET, amyloid PET, T1W, and high-resolution T2W scans. Clinical symptoms were assessed by the Neuropsychiatric Inventory (NPI) total score and Alzheimer’s Disease Assessment Scale cognition 13 (ADAS-cog-13) total score, comprising memory and executive function scores. The hippocampal subfields including Cornu Ammonis (CA1–3), subiculum (Sub), and dentate gyrus (DG), as well as the adjacent para-hippocampus (PHC) and entorhinal cortex (ERC), were segmented automatically using the Automatic Segmentation of Hippocampal Subfields (ASHS) software. The relationship between tauopathy/volume of the hippocampal subfields and assessment scores was calculated using partial correlation analysis under different amyloid status, by controlling age, gender, education, apolipoprotein E (APOE) allele ɛ4 carrier status, and, time interval between the acquisition time of tau PET and amyloid PET scans. Results: Compared with amyloid negative (A−) group, individuals from amyloid positive (A+) group are more impaired based on the Mini-mental State Examination (MMSE; p = 3.82e-05), memory (p = 6.30e-04), executive function (p = 0.0016), and ADAS-cog-13 scores (p = 5.11e-04). Significant decrease of volume (CA1, DG, and Sub) and increase of tau deposition (CA1, Sub, ERC, and PHC) of the hippocampal subfields of both hemispheres were observed for the A+ group compared to the A- group. Tauopathy of ERC is significantly associated with memory score for the A- group, and the associated regions spread into Sub and PHC for the A+ group. The relationship between the impairment of behavior or executive function and tauopathy of the hippocampal subfield was discovered within the A+ group. Leftward asymmetry was observed with the association between assessment scores and tauopathy of the hippocampal subfield, which is more prominent for the NPI score for the A+ group. Conclusion: The associations of tauopathy/volume of the hippocampal subfields with clinical symptoms provide additional insight into the understanding of local changes of the human HF during the AD continuum and can be used as a reference for future studies. Frontiers Media S.A. 2021-07-14 /pmc/articles/PMC8317580/ /pubmed/34335226 http://dx.doi.org/10.3389/fnagi.2021.672077 Text en Copyright © 2021 Ge, Zhang, Qiao, Zhang, Xu and Zheng. https://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(s) 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
Ge, Xinting
Zhang, Dan
Qiao, Yuchuan
Zhang, Jiong
Xu, Junhai
Zheng, Yuanjie
Association of Tau Pathology With Clinical Symptoms in the Subfields of Hippocampal Formation
title Association of Tau Pathology With Clinical Symptoms in the Subfields of Hippocampal Formation
title_full Association of Tau Pathology With Clinical Symptoms in the Subfields of Hippocampal Formation
title_fullStr Association of Tau Pathology With Clinical Symptoms in the Subfields of Hippocampal Formation
title_full_unstemmed Association of Tau Pathology With Clinical Symptoms in the Subfields of Hippocampal Formation
title_short Association of Tau Pathology With Clinical Symptoms in the Subfields of Hippocampal Formation
title_sort association of tau pathology with clinical symptoms in the subfields of hippocampal formation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317580/
https://www.ncbi.nlm.nih.gov/pubmed/34335226
http://dx.doi.org/10.3389/fnagi.2021.672077
work_keys_str_mv AT gexinting associationoftaupathologywithclinicalsymptomsinthesubfieldsofhippocampalformation
AT zhangdan associationoftaupathologywithclinicalsymptomsinthesubfieldsofhippocampalformation
AT qiaoyuchuan associationoftaupathologywithclinicalsymptomsinthesubfieldsofhippocampalformation
AT zhangjiong associationoftaupathologywithclinicalsymptomsinthesubfieldsofhippocampalformation
AT xujunhai associationoftaupathologywithclinicalsymptomsinthesubfieldsofhippocampalformation
AT zhengyuanjie associationoftaupathologywithclinicalsymptomsinthesubfieldsofhippocampalformation