Cargando…

Alzheimer’s Biomarkers are Correlated with Brain Connectivity in Older Adults Differentially during Resting and Task States

β-amyloid (Aβ) plaques and tau-related neurodegeneration are pathologic hallmarks of Alzheimer’s disease (AD). The utility of AD biomarkers, including those measured in cerebrospinal fluid (CSF), in predicting future AD risk and cognitive decline is still being refined. Here, we explored potential r...

Descripción completa

Detalles Bibliográficos
Autores principales: Jiang, Yang, Huang, Haiqing, Abner, Erin, Broster, Lucas S., Jicha, Gregory A., Schmitt, Frederick A., Kryscio, Richard, Andersen, Anders, Powell, David, Van Eldik, Linda, Gold, Brian T., Nelson, Peter T., Smith, Charles, Ding, Mingzhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744860/
https://www.ncbi.nlm.nih.gov/pubmed/26903858
http://dx.doi.org/10.3389/fnagi.2016.00015
_version_ 1782414538864328704
author Jiang, Yang
Huang, Haiqing
Abner, Erin
Broster, Lucas S.
Jicha, Gregory A.
Schmitt, Frederick A.
Kryscio, Richard
Andersen, Anders
Powell, David
Van Eldik, Linda
Gold, Brian T.
Nelson, Peter T.
Smith, Charles
Ding, Mingzhou
author_facet Jiang, Yang
Huang, Haiqing
Abner, Erin
Broster, Lucas S.
Jicha, Gregory A.
Schmitt, Frederick A.
Kryscio, Richard
Andersen, Anders
Powell, David
Van Eldik, Linda
Gold, Brian T.
Nelson, Peter T.
Smith, Charles
Ding, Mingzhou
author_sort Jiang, Yang
collection PubMed
description β-amyloid (Aβ) plaques and tau-related neurodegeneration are pathologic hallmarks of Alzheimer’s disease (AD). The utility of AD biomarkers, including those measured in cerebrospinal fluid (CSF), in predicting future AD risk and cognitive decline is still being refined. Here, we explored potential relationships between functional connectivity (FC) patterns within the default-mode network (DMN), age, CSF biomarkers (Aβ(42) and pTau(181)), and cognitive status in older adults. Multiple measures of FC were explored, including a novel time series-based measure [total interdependence (TI)]. In our sample of 27 cognitively normal older adults, no significant associations were found between levels of Aβ(42) or pTau(181) and cognitive scores or regional brain volumes. However, we observed several novel relationships between these biomarkers and measures of FC in DMN during both resting-state and a short-term memory task. First, increased connectivity between bilateral anterior middle temporal gyri was associated with higher levels of CSF Aβ(42) and Aβ(42)/pTau(181) ratio (reflecting lower AD risk) during both rest and task. Second, increased bilateral parietal connectivity during the short-term memory task, but not during rest, was associated with higher levels of CSF pTau(181) (reflecting higher AD risk). Third, increased connectivity between left middle temporal and left parietal cortices during the active task was associated with decreased global cognitive status but not CSF biomarkers. Lastly, we found that our new TI method was more sensitive to the CSF Aβ(42)-connectivity relationship whereas the traditional cross-correlation method was more sensitive to levels of CSF pTau(181) and cognitive status. With further refinement, resting-state connectivity and task-driven connectivity measures hold promise as non-invasive neuroimaging markers of Aβ and pTau burden in cognitively normal older adults.
format Online
Article
Text
id pubmed-4744860
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-47448602016-02-22 Alzheimer’s Biomarkers are Correlated with Brain Connectivity in Older Adults Differentially during Resting and Task States Jiang, Yang Huang, Haiqing Abner, Erin Broster, Lucas S. Jicha, Gregory A. Schmitt, Frederick A. Kryscio, Richard Andersen, Anders Powell, David Van Eldik, Linda Gold, Brian T. Nelson, Peter T. Smith, Charles Ding, Mingzhou Front Aging Neurosci Neuroscience β-amyloid (Aβ) plaques and tau-related neurodegeneration are pathologic hallmarks of Alzheimer’s disease (AD). The utility of AD biomarkers, including those measured in cerebrospinal fluid (CSF), in predicting future AD risk and cognitive decline is still being refined. Here, we explored potential relationships between functional connectivity (FC) patterns within the default-mode network (DMN), age, CSF biomarkers (Aβ(42) and pTau(181)), and cognitive status in older adults. Multiple measures of FC were explored, including a novel time series-based measure [total interdependence (TI)]. In our sample of 27 cognitively normal older adults, no significant associations were found between levels of Aβ(42) or pTau(181) and cognitive scores or regional brain volumes. However, we observed several novel relationships between these biomarkers and measures of FC in DMN during both resting-state and a short-term memory task. First, increased connectivity between bilateral anterior middle temporal gyri was associated with higher levels of CSF Aβ(42) and Aβ(42)/pTau(181) ratio (reflecting lower AD risk) during both rest and task. Second, increased bilateral parietal connectivity during the short-term memory task, but not during rest, was associated with higher levels of CSF pTau(181) (reflecting higher AD risk). Third, increased connectivity between left middle temporal and left parietal cortices during the active task was associated with decreased global cognitive status but not CSF biomarkers. Lastly, we found that our new TI method was more sensitive to the CSF Aβ(42)-connectivity relationship whereas the traditional cross-correlation method was more sensitive to levels of CSF pTau(181) and cognitive status. With further refinement, resting-state connectivity and task-driven connectivity measures hold promise as non-invasive neuroimaging markers of Aβ and pTau burden in cognitively normal older adults. Frontiers Media S.A. 2016-02-08 /pmc/articles/PMC4744860/ /pubmed/26903858 http://dx.doi.org/10.3389/fnagi.2016.00015 Text en Copyright © 2016 Jiang, Huang, Abner, Broster, Jicha, Schmitt, Kryscio, Andersen, Powell, Van Eldik, Gold, Nelson, Smith and Ding. 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) or licensor 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
Jiang, Yang
Huang, Haiqing
Abner, Erin
Broster, Lucas S.
Jicha, Gregory A.
Schmitt, Frederick A.
Kryscio, Richard
Andersen, Anders
Powell, David
Van Eldik, Linda
Gold, Brian T.
Nelson, Peter T.
Smith, Charles
Ding, Mingzhou
Alzheimer’s Biomarkers are Correlated with Brain Connectivity in Older Adults Differentially during Resting and Task States
title Alzheimer’s Biomarkers are Correlated with Brain Connectivity in Older Adults Differentially during Resting and Task States
title_full Alzheimer’s Biomarkers are Correlated with Brain Connectivity in Older Adults Differentially during Resting and Task States
title_fullStr Alzheimer’s Biomarkers are Correlated with Brain Connectivity in Older Adults Differentially during Resting and Task States
title_full_unstemmed Alzheimer’s Biomarkers are Correlated with Brain Connectivity in Older Adults Differentially during Resting and Task States
title_short Alzheimer’s Biomarkers are Correlated with Brain Connectivity in Older Adults Differentially during Resting and Task States
title_sort alzheimer’s biomarkers are correlated with brain connectivity in older adults differentially during resting and task states
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744860/
https://www.ncbi.nlm.nih.gov/pubmed/26903858
http://dx.doi.org/10.3389/fnagi.2016.00015
work_keys_str_mv AT jiangyang alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT huanghaiqing alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT abnererin alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT brosterlucass alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT jichagregorya alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT schmittfredericka alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT krysciorichard alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT andersenanders alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT powelldavid alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT vaneldiklinda alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT goldbriant alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT nelsonpetert alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT smithcharles alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates
AT dingmingzhou alzheimersbiomarkersarecorrelatedwithbrainconnectivityinolderadultsdifferentiallyduringrestingandtaskstates