TY - JOUR
T1 - Functional brain connectivity using fMRI in aging and Alzheimer's disease
AU - Dennis, Emily L.
AU - Thompson, Paul M.
N1 - Funding Information:
Acknowledgments ED was funded, in part, by an NIH Training Grant in Neurobehavioral Genetics (T32 MH073526-06), and by the Betty B. and James B. Lambert Scholarship from the Kappa Alpha Theta Foundation. The authors were also supported by NIH R01 grants EB008432, EB008281, EB007813 and P41 RR013642.
PY - 2014/3
Y1 - 2014/3
N2 - Normal aging and Alzheimer's disease (AD) cause profound changes in the brain's structure and function. AD in particular is accompanied by widespread cortical neuronal loss, and loss of connections between brain systems. This degeneration of neural pathways disrupts the functional coherence of brain activation. Recent innovations in brain imaging have detected characteristic disruptions in functional networks. Here we review studies examining changes in functional connectivity, measured through fMRI (functional magnetic resonance imaging), starting with healthy aging and then Alzheimer's disease. We cover studies that employ the three primary methods to analyze functional connectivity - seed-based, ICA (independent components analysis), and graph theory. At the end we include a brief discussion of other methodologies, such as EEG (electroencephalography), MEG (magnetoencephalography), and PET (positron emission tomography). We also describe multi-modal studies that combine rsfMRI (resting state fMRI) with PET imaging, as well as studies examining the effects of medications. Overall, connectivity and network integrity appear to decrease in healthy aging, but this decrease is accelerated in AD, with specific systems hit hardest, such as the default mode network (DMN). Functional connectivity is a relatively new topic of research, but it holds great promise in revealing how brain network dynamics change across the lifespan and in disease.
AB - Normal aging and Alzheimer's disease (AD) cause profound changes in the brain's structure and function. AD in particular is accompanied by widespread cortical neuronal loss, and loss of connections between brain systems. This degeneration of neural pathways disrupts the functional coherence of brain activation. Recent innovations in brain imaging have detected characteristic disruptions in functional networks. Here we review studies examining changes in functional connectivity, measured through fMRI (functional magnetic resonance imaging), starting with healthy aging and then Alzheimer's disease. We cover studies that employ the three primary methods to analyze functional connectivity - seed-based, ICA (independent components analysis), and graph theory. At the end we include a brief discussion of other methodologies, such as EEG (electroencephalography), MEG (magnetoencephalography), and PET (positron emission tomography). We also describe multi-modal studies that combine rsfMRI (resting state fMRI) with PET imaging, as well as studies examining the effects of medications. Overall, connectivity and network integrity appear to decrease in healthy aging, but this decrease is accelerated in AD, with specific systems hit hardest, such as the default mode network (DMN). Functional connectivity is a relatively new topic of research, but it holds great promise in revealing how brain network dynamics change across the lifespan and in disease.
KW - Aging
KW - Alzheimer's
KW - Functional connectivity
KW - Graph theory
KW - ICA
KW - Resting state
KW - Seed-based
KW - fMRI
UR - http://www.scopus.com/inward/record.url?scp=84897606134&partnerID=8YFLogxK
U2 - 10.1007/s11065-014-9249-6
DO - 10.1007/s11065-014-9249-6
M3 - Review article
C2 - 24562737
AN - SCOPUS:84897606134
SN - 1040-7308
VL - 24
SP - 49
EP - 62
JO - Neuropsychology Review
JF - Neuropsychology Review
IS - 1
ER -