TY - JOUR
T1 - Forecasting memory function in aging
T2 - pattern-completion ability and hippocampal activity relate to visuospatial functioning over 25 years
AU - Nyberg, Lars
AU - Grande, Xenia
AU - Andersson, Micael
AU - Berron, David
AU - Lundquist, Anders
AU - Stiernstedt, Mikael
AU - Fjell, Anders
AU - Walhovd, Kristine
AU - Orädd, Greger
PY - 2020
Y1 - 2020
N2 - Heterogeneity in episodic memory functioning in aging was assessed with a pattern-completion functional magnetic resonance imaging task that required reactivation of well-consolidated face-name memory traces from fragmented (partial) or morphed (noisy) face cues. About half of the examined individuals (N = 101) showed impaired (chance) performance on fragmented faces despite intact performance on complete and morphed faces, and they did not show a pattern-completion response in hippocampus or the examined subfields (CA1, CA23, DGCA4). This apparent pattern-completion deficit could not be explained by differential hippocampal atrophy. Instead, the impaired group displayed lower cortical volumes, accelerated reduction in mini-mental state examination scores, and lower general cognitive function as defined by longitudinal measures of visuospatial functioning and speed-of-processing. In the full sample, inter-individual differences in visuospatial functioning predicted performance on fragmented faces and hippocampal CA23 subfield activity over 25 years. These findings suggest that visuospatial functioning in middle age can forecast pattern-completion deficits in aging.
AB - Heterogeneity in episodic memory functioning in aging was assessed with a pattern-completion functional magnetic resonance imaging task that required reactivation of well-consolidated face-name memory traces from fragmented (partial) or morphed (noisy) face cues. About half of the examined individuals (N = 101) showed impaired (chance) performance on fragmented faces despite intact performance on complete and morphed faces, and they did not show a pattern-completion response in hippocampus or the examined subfields (CA1, CA23, DGCA4). This apparent pattern-completion deficit could not be explained by differential hippocampal atrophy. Instead, the impaired group displayed lower cortical volumes, accelerated reduction in mini-mental state examination scores, and lower general cognitive function as defined by longitudinal measures of visuospatial functioning and speed-of-processing. In the full sample, inter-individual differences in visuospatial functioning predicted performance on fragmented faces and hippocampal CA23 subfield activity over 25 years. These findings suggest that visuospatial functioning in middle age can forecast pattern-completion deficits in aging.
KW - Episodic memory
KW - General cognitive function
KW - Hippocampus
KW - Subfields
U2 - 10.1016/j.neurobiolaging.2020.06.005
DO - 10.1016/j.neurobiolaging.2020.06.005
M3 - Article
C2 - 32650185
AN - SCOPUS:85087497619
SN - 0197-4580
VL - 94
SP - 217
EP - 226
JO - Neurobiology of Aging
JF - Neurobiology of Aging
ER -