Identifying brain networks in synaptic density PET ((11)C-UCB-J) with independent component analysis.
Identifying brain networks in synaptic density PET ((11)C-UCB-J) with independent component analysis.
复制标题
DOI:
10.1016/j.neuroimage.2021.118167
复制
发表时间:
2021-08-15
期刊:
影响因子:
5.7
通讯作者:
Carson RE
中科院分区:
文献类型:
--
作者:
Fang XT;Toyonaga T;Hillmer AT;Matuskey D;Holmes SE;Radhakrishnan R;Mecca AP;van Dyck CH;D'Souza DC;Esterlis I;Worhunsky PD;Carson RE
The human brain is inherently organized into distinct networks, as reported widely by resting-state functional magnetic resonance imaging (rs-fMRI), which are based on blood-oxygen-level-dependent (BOLD) signal fluctuations. 11C-UCB-J PET maps synaptic density via synaptic vesicle protein 2A, which is a more direct structural measure underlying brain networks than BOLD rs-fMRI. The aim of this study was to identify maximally independent brain source networks, i.e., “spatial patterns with common covariance across subjects”, in 11C-UCB-J data using independent component analysis (ICA), a data-driven analysis method. Using a population of 80 healthy controls, we applied ICA to two 40-sample subsets and compared source network replication across samples. We examined the identified source networks at multiple model orders, as the ideal number of maximally independent components (IC) is unknown. In addition we investigated the relationship between the strength of the loading weights for each source network and age and sex. Thirteen source networks replicated across both samples. We determined that a model order of 18 components provided stable, replicable components, whereas estimations above 18 were not stable. Effects of sex were found in two ICs. Nine ICs showed age-related change, with 4 remaining significant after correction for multiple comparison. This study provides the first evidence that human brain synaptic density can be characterized into organized covariance patterns. Furthermore, we demonstrated that multiple synaptic density source networks are associated with age, which supports the potential utility of ICA to identify biologically relevant synaptic density source networks.
登录
查看更多内容
影响因子:
11
作者:
D'Souza, Deepak Cyril;Radhakrishnan, Rajiv;Skosnik, Patrick
通讯作者:
Skosnik, Patrick
影响因子:
17.1
作者:
Finnema, Sjoerd J.;Nabulsi, Nabeel B.;Carson, Richard E.
通讯作者:
Carson, Richard E.
影响因子:
3.2
作者:
Laird AR;Fox PM;Eickhoff SB;Turner JA;Ray KL;McKay DR;Glahn DC;Beckmann CF;Smith SM;Fox PT
通讯作者:
Fox PT
影响因子:
4.8
作者:
Abou-Elseoud, Ahmed;Starck, Tuomo;Kiviniemi, Vesa
通讯作者:
Kiviniemi, Vesa
影响因子:
29
作者:
Chen, Ming-Kai;Mecca, Adam P.;van Dyck, Christopher H.
通讯作者:
van Dyck, Christopher H.