TY - JOUR
T1 - Single-subject Single-session Temporally-Independent Functional Modes of Brain Activity
AU - Gomez, Daniel E.P.
AU - Llera, Alberto
AU - Marques, José P.R.F.
AU - Beckmann, Christian F.
AU - Norris, David G.
PY - 2020/9/1
Y1 - 2020/9/1
N2 - Temporally independent functional modes (TFMs) are functional brain networks identified based on their temporal independence. The rationale behind identifying TFMs is that different functional networks may share a common anatomical infrastructure yet display distinct temporal dynamics. Extracting TFMs usually require a larger number of samples than acquired in standard fMRI experiments, and thus have therefore previously only been performed at the group level. Here, using an ultra-fast fMRI sequence, MESH-EPI, with a volume repetition time of 158 ms, we conducted an exploratory study with n = 6 subjects and computed TFMs at the single subject level on both task and resting-state datasets. We identified 6 common temporal modes of activity in our participants, including a temporal default mode showing patterns of anti-correlation between the default mode and the task-positive networks, a lateralised motor mode and a visual mode integrating the visual cortex and the visual streams. In alignment with other findings reported recently, we also showed that independent time-series are largely free from confound contamination. In particular for ultra-fast fMRI, TFMs can separate the cardiac signal from other fluctuations. Using a non-linear dimensionality reduction technique, UMAP, we obtained preliminary evidence that combinations of spatial networks as described by the TFM model are highly individual. Our results show that it is feasible to measure reproducible TFMs at the single-subject level, opening new possibilities for investigating functional networks and their integration. Finally, we provide a python toolbox for generating TFMs and comment on possible applications of the technique and avenues for further investigation.
AB - Temporally independent functional modes (TFMs) are functional brain networks identified based on their temporal independence. The rationale behind identifying TFMs is that different functional networks may share a common anatomical infrastructure yet display distinct temporal dynamics. Extracting TFMs usually require a larger number of samples than acquired in standard fMRI experiments, and thus have therefore previously only been performed at the group level. Here, using an ultra-fast fMRI sequence, MESH-EPI, with a volume repetition time of 158 ms, we conducted an exploratory study with n = 6 subjects and computed TFMs at the single subject level on both task and resting-state datasets. We identified 6 common temporal modes of activity in our participants, including a temporal default mode showing patterns of anti-correlation between the default mode and the task-positive networks, a lateralised motor mode and a visual mode integrating the visual cortex and the visual streams. In alignment with other findings reported recently, we also showed that independent time-series are largely free from confound contamination. In particular for ultra-fast fMRI, TFMs can separate the cardiac signal from other fluctuations. Using a non-linear dimensionality reduction technique, UMAP, we obtained preliminary evidence that combinations of spatial networks as described by the TFM model are highly individual. Our results show that it is feasible to measure reproducible TFMs at the single-subject level, opening new possibilities for investigating functional networks and their integration. Finally, we provide a python toolbox for generating TFMs and comment on possible applications of the technique and avenues for further investigation.
KW - connectivity
KW - fmri
KW - mesh
KW - multiband
KW - resting-state
KW - sms
KW - tfm
KW - Ultra-fast
UR - http://www.scopus.com/inward/record.url?scp=85085842331&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2020.116783
DO - 10.1016/j.neuroimage.2020.116783
M3 - Article
C2 - 32413462
AN - SCOPUS:85085842331
SN - 1053-8119
VL - 218
JO - NeuroImage
JF - NeuroImage
M1 - 116783
ER -