TY - JOUR
T1 - Decreased fronto-parietal and increased default mode network activation is associated with subtle cognitive deficits in elderly controls
AU - Zanchi, Davide
AU - Montandon, Marie Louise
AU - Sinanaj, Indrit
AU - Rodriguez, Cristelle
AU - Depoorter, Antoinette
AU - Herrmann, Francois R.
AU - Borgwardt, Stefan
AU - Giannakopoulos, Panteleimon
AU - Haller, Sven
N1 - Publisher Copyright:
© 2017 The Author(s) Published by S. Karger AG, Basel.
PY - 2018/1/1
Y1 - 2018/1/1
N2 - Background: Cognitive functions progressively deteriorate during aging and neurodegener-Ative diseases. The present study aims at investigating differences in working memory per-formance as well as functional brain changes during the earliest stages of cognitive decline in health elderly individuals. Methods: 62 elderly individuals (41 females), including 41 controls (35 females) and 21 middle cognitive impairment subjects (6 females), underwent neuropsychological assessment at baseline and an fMRI examination in a N-back paradigm contrasting 2-back vs. 0-back condition. Upon a 18 months follow-up, we identified stable controls (sCON) with preserved cognition and deteriorating controls (dCON) with -1SD decrease of performances in at least two neuropsychological tests. Data analyses included accuracy and reaction time (RT) for the 2-back condition and general linear model (GLM) for the fMRI sequence. Results: At the behavioral level, sCON and dCON performed better than MCI in terms of accuracy and reaction time. At the brain level, functional differences in regions of the fronto-parietal network (FPN) and of the Default Mode Network (DFM) were observed. Significantly lower neural activations in the bilateral inferior and middle frontal gyri were found in MCI versus both dCON / sCON and for dCON versus sCON. Significantly increased activations in the anterior cingulate cortex and posterior cingulate cortex and bilateral insula were found in MCI versus both dCON / sCON and in dCON versus sCON. Conclusion: The present study suggests that brain functional changes in FPN and DMN anticipate differences in cognitive performance in healthy elderly individuals with subsequent subtle cognitive decline.
AB - Background: Cognitive functions progressively deteriorate during aging and neurodegener-Ative diseases. The present study aims at investigating differences in working memory per-formance as well as functional brain changes during the earliest stages of cognitive decline in health elderly individuals. Methods: 62 elderly individuals (41 females), including 41 controls (35 females) and 21 middle cognitive impairment subjects (6 females), underwent neuropsychological assessment at baseline and an fMRI examination in a N-back paradigm contrasting 2-back vs. 0-back condition. Upon a 18 months follow-up, we identified stable controls (sCON) with preserved cognition and deteriorating controls (dCON) with -1SD decrease of performances in at least two neuropsychological tests. Data analyses included accuracy and reaction time (RT) for the 2-back condition and general linear model (GLM) for the fMRI sequence. Results: At the behavioral level, sCON and dCON performed better than MCI in terms of accuracy and reaction time. At the brain level, functional differences in regions of the fronto-parietal network (FPN) and of the Default Mode Network (DFM) were observed. Significantly lower neural activations in the bilateral inferior and middle frontal gyri were found in MCI versus both dCON / sCON and for dCON versus sCON. Significantly increased activations in the anterior cingulate cortex and posterior cingulate cortex and bilateral insula were found in MCI versus both dCON / sCON and in dCON versus sCON. Conclusion: The present study suggests that brain functional changes in FPN and DMN anticipate differences in cognitive performance in healthy elderly individuals with subsequent subtle cognitive decline.
UR - http://www.scopus.com/inward/record.url?scp=85038636199&partnerID=8YFLogxK
U2 - 10.1159/000486152
DO - 10.1159/000486152
M3 - Journal articles
C2 - 29268260
AN - SCOPUS:85038636199
SN - 1424-862X
VL - 25
SP - 127
EP - 138
JO - NeuroSignals
JF - NeuroSignals
IS - 1
ER -