TY - JOUR
T1 - Multimodal neuroimaging analysis reveals age-associated common and discrete cognitive control constructs
AU - Yang, Meng Heng
AU - Yao, Zai Fu
AU - Hsieh, Shulan
N1 - Funding Information:
This work was supported by the Ministry of Science and Technology (MOST), Taiwan, for financially supporting this research (Contract No. 104-2410-H-006-021-MY2 & 106-2410-H-006-031-MY2). We thank Frini Karayanidis, Birte Forstmann, Alexander Conley, and Wou-ter Boekel for their great help in setting up this study and Hsing-Hao Lee, Yu-Chi Lin, and Yenting Yu for their help in collecting data. We also thank Howard Hsu for his help in generating supplemental figures during the revision. We thank the Mind Research and Imaging Center (MRIC), supported by MOST, at NCKU for consultation and instrument availability.
Publisher Copyright:
© 2019 Wiley Periodicals, Inc.
PY - 2019/6/15
Y1 - 2019/6/15
N2 - The aims of this study were to determine which cognitive control functions are most sensitive to cross-sectional age differences and to identify neural features in different neuroimaging modalities that associated cognitive control function across the adult lifespan. We employed a joint independent component analysis (jICA) approach to obtain common networks among three different brain-imaging modalities (i.e., structural MRI, resting-state functional MRI, and diffusion tensor imaging) in relation to the cognitive control function. We differentiated three distinct cognitive constructs: one common (across inhibition, shifting, and updating) and two specific (shifting, updating) factors. These common/specific constructs were transformed from three original performance indexes: (a) stop-signal reaction time, (b) switch-cost, and (c) performance sensitivity collected from 156 individuals aged 20 to 78 years old. The current results show that the cross-sectional age difference is associated with a wide spread of brain degeneration that is not limited to the frontal region. Crucially, these findings suggest there are some common and distinct joined multimodal components that correlate with the psychological constructs of common and discrete cognitive control functions, respectively. To support current findings, other fusion ICA models were also analyzed including, parallel ICA (para-ICA) and multiset canonical correlation analysis with jICA (mCCA + jICA). Dynamic interactions among these brain features across different brain modalities could serve as possible developmental mechanisms associated with these age effects.
AB - The aims of this study were to determine which cognitive control functions are most sensitive to cross-sectional age differences and to identify neural features in different neuroimaging modalities that associated cognitive control function across the adult lifespan. We employed a joint independent component analysis (jICA) approach to obtain common networks among three different brain-imaging modalities (i.e., structural MRI, resting-state functional MRI, and diffusion tensor imaging) in relation to the cognitive control function. We differentiated three distinct cognitive constructs: one common (across inhibition, shifting, and updating) and two specific (shifting, updating) factors. These common/specific constructs were transformed from three original performance indexes: (a) stop-signal reaction time, (b) switch-cost, and (c) performance sensitivity collected from 156 individuals aged 20 to 78 years old. The current results show that the cross-sectional age difference is associated with a wide spread of brain degeneration that is not limited to the frontal region. Crucially, these findings suggest there are some common and distinct joined multimodal components that correlate with the psychological constructs of common and discrete cognitive control functions, respectively. To support current findings, other fusion ICA models were also analyzed including, parallel ICA (para-ICA) and multiset canonical correlation analysis with jICA (mCCA + jICA). Dynamic interactions among these brain features across different brain modalities could serve as possible developmental mechanisms associated with these age effects.
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U2 - 10.1002/hbm.24550
DO - 10.1002/hbm.24550
M3 - Article
C2 - 30779255
AN - SCOPUS:85061926214
SN - 1065-9471
VL - 40
SP - 2639
EP - 2661
JO - Human Brain Mapping
JF - Human Brain Mapping
IS - 9
ER -