TY - JOUR
T1 - Disruptions in brain networks of older fallers are associated with subsequent cognitive decline
T2 - A 12-month prospective exploratory study
AU - Hsu, Chun Liang
AU - Voss, Michelle W.
AU - Handy, Todd C.
AU - Davis, Jennifer C.
AU - Nagamatsu, Lindsay S.
AU - Chan, Alison
AU - Bolandzadeh, Niousha
AU - Liu-Ambrose, Teresa
N1 - Funding Information:
Teresa Liu-Ambrose is a Canada Research Chair in Physical Activity, Mobility, and Cognitive Neuroscience, a Michael Smith Foundation for Health Research (MSFHR) Scholar, a Canadian Institutes of Health Research (CIHR) New Investigator, and a Heart and Stroke Foundation of Canada’s (HSFC) Henry JM Barnett’s Scholarship recipient. Jennifer Davis is a MSFHR and a CIHR Post-Doctoral Fellow. Lindsay Nagamatsu is a MSFHR Senior Graduate trainee and a Natural Sciences and Engineering Research Council of Canada Doctoral trainee. Niousha Bolandzadeh is a HSFC Doctoral trainee. Chun Liang Hsu is an Alzheimer’s Society Research Program Doctoral trainee.
PY - 2014/4/3
Y1 - 2014/4/3
N2 - Cognitive impairment and impaired mobility are major public health concerns. There is growing recognition that impaired mobility is an early biomarker of cognitive impairment and dementia. The neural basis for this association is currently unclear. We propose disrupted functional connectivity as a potential mechanism. In this 12-month prospective exploratory study, we compared functional connectivity of four brain networks- the default mode network (DMN), fronto-executive network (FEN), fronto-parietal network (FPN), and the primary motor sensory network (SMN) - between community-dwelling older adults with ≥ two falls in the last 12 months and their non-falling counterparts (≤ one fall in the last 12 months). Functional connectivity was examined both at rest and during a simple motor tapping task. Compared with non-fallers, fallers showed more connectivity between the DMN and FPN during right finger tapping (p = 0.04), and significantly less functional connectivity between the SMN and FPN during rest (p≤0.05). Less connectivity between the SMN and FPN during rest was significantly associated with greater decline in both cognitive function and mobility over the12-month period (r = -0.32 and 0.33 respectively; p≤0.04). Thus, a recent history of multiple falls among older adults without a diagnosis of dementia may indicate sub-clinical changes in brain function and increased risk for subsequent decline.
AB - Cognitive impairment and impaired mobility are major public health concerns. There is growing recognition that impaired mobility is an early biomarker of cognitive impairment and dementia. The neural basis for this association is currently unclear. We propose disrupted functional connectivity as a potential mechanism. In this 12-month prospective exploratory study, we compared functional connectivity of four brain networks- the default mode network (DMN), fronto-executive network (FEN), fronto-parietal network (FPN), and the primary motor sensory network (SMN) - between community-dwelling older adults with ≥ two falls in the last 12 months and their non-falling counterparts (≤ one fall in the last 12 months). Functional connectivity was examined both at rest and during a simple motor tapping task. Compared with non-fallers, fallers showed more connectivity between the DMN and FPN during right finger tapping (p = 0.04), and significantly less functional connectivity between the SMN and FPN during rest (p≤0.05). Less connectivity between the SMN and FPN during rest was significantly associated with greater decline in both cognitive function and mobility over the12-month period (r = -0.32 and 0.33 respectively; p≤0.04). Thus, a recent history of multiple falls among older adults without a diagnosis of dementia may indicate sub-clinical changes in brain function and increased risk for subsequent decline.
UR - http://www.scopus.com/inward/record.url?scp=84899414768&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0093673
DO - 10.1371/journal.pone.0093673
M3 - Journal article
C2 - 24699668
AN - SCOPUS:84899414768
SN - 1932-6203
VL - 9
JO - PLoS ONE
JF - PLoS ONE
IS - 4
M1 - e93673
ER -