Poster No:
976
Submission Type:
Abstract Submission
Authors:
Qiongling Li1, Lianglong Sun1, Xinyuan Liang1, Debin Zeng2, Mingrui Xia1, Shuyu Li1, Yong He1
Institutions:
1State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, Beijing, 2School of Biological Science & Medical Engineering, Beihang University, Beijing, Beijing
First Author:
Qiongling Li
State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University
Beijing, Beijing
Co-Author(s):
Lianglong Sun
State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University
Beijing, Beijing
Xinyuan Liang
State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University
Beijing, Beijing
Debin Zeng
School of Biological Science & Medical Engineering, Beihang University
Beijing, Beijing
Mingrui Xia
State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University
Beijing, Beijing
Shuyu Li
State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University
Beijing, Beijing
Yong He
State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University
Beijing, Beijing
Introduction:
A fundamental aspect of understanding the principle of the human brain organization is the unfolding of the intrinsic functional architecture of the cerebral cortex. Functional gradients allow for the representation of indispensable spatial topography of brain organization at a macroscale, which can be derived from the coherent intrinsic or spontaneous brain activity 1,2. Among these gradients, the sensorimotor-association (S-A) gradient captures the principal axis of cortical functional differentiation spanning from low-order primary to high-order association cortices 3. This cortex-wide embedding optimizes the continuity of function between adjacent areas and subserves the cognitive spectrum from sensation, perception, and action to abstract cognition along the cortical mantle 3. As a fundamental organizational principle, the principal S-A gradient of functional connectome conforms to spatial variations in a number of neurobiological features, including macrostructural cortical thickness 4, and microstructural intracortical myelination 5. Despite its importance, how the S-A axis of cortical functional organization is established and evolves across the lifespan remains largely unknown.
Methods:
Following a rigorous quality control procedure, we included a large multimodal structural MRI and task-free fMRI dataset from 33,247 participants aged 32 postmenstrual weeks to 80 years. Using diffusion map embedding approaches, we obtained functional gradients from both age-specific, group-level connectomes and person-specific connectomes. We also investigated how the maturation of the cortex-wide S-A gradient across the lifespan is associated with changes in structural properties including intrinsic geometric distance, macrostructural cortical thickness, and microstructural intracortical myelination.
Results:
The functional connectome gradient initially manifests as an anterior-posterior differentiation and then progresses through a canonical S-A differentiation (Fig. 1A). The functional gradients across different age groups were found to be categorized into three distinct stages (Fig. 1B): (i) Stage 1, termed "initiation", involving broad anterior-posterior differentiation; (ii) Stage 2, termed "establishment", transitioning from anterior-posterior patterns into canonical primary-association gradient; (iii) Stage 3, termed "expansion and stability", undergoing further expansion and fine-tuning, achieving a more stable and mature configuration, until degeneration during aging (Fig. 1C).
We found the robust coupling between intrinsic geometry and cortical functional differentiation of the S-A axis where the correlations remained high (r>0.90) throughout the lifespan. Nonetheless, this correlation tended to decrease until late adolescence and then showed little change thereafter (Fig. 2A). This result suggests that the geometric constraints on functional differentiation of the S-A axis gradually decrease with development, possibly allowing for greater cognitive flexibility.
The S-A connectome gradient maps showed significant spatial correlations with cortical thickness maps (Fig. 2D) and intracortical myelination maps (Fig. 2E) across the lifespan, especially during the first two decades. The growth rate of the S-A gradient of functional connectome was significantly correlated with the growth rate of cortical thickness during late childhood, adolescence, and early adulthood (Fig. 2E), and the growth rate of intracortical myelination during adolescence and early adulthood (Fig. 2F). During aging, the correlation between these growth rates of functional gradient and intracortical myelination persisted, albeit with a weaker effect size. These results suggest a synchronous maturation of cortical functional hierarchy with cytoarchitectural and myeloarchitectural hierarchies during adolescence and early adulthood.


Conclusions:
Our results identified critical windows of the sensorimotor-association gradient growth, and its structural basis throughout the human lifespan.
Lifespan Development:
Early life, Adolescence, Aging 1
Modeling and Analysis Methods:
Connectivity (eg. functional, effective, structural) 2
fMRI Connectivity and Network Modeling
Novel Imaging Acquisition Methods:
BOLD fMRI
Keywords:
Other - functional connectome
1|2Indicates the priority used for review
By submitting your proposal, you grant permission for the Organization for Human Brain Mapping (OHBM) to distribute your work in any format, including video, audio print and electronic text through OHBM OnDemand, social media channels, the OHBM website, or other electronic publications and media.
I accept
The Open Science Special Interest Group (OSSIG) is introducing a reproducibility challenge for OHBM 2025. This new initiative aims to enhance the reproducibility of scientific results and foster collaborations between labs. Teams will consist of a “source” party and a “reproducing” party, and will be evaluated on the success of their replication, the openness of the source work, and additional deliverables. Click here for more information.
Propose your OHBM abstract(s) as source work for future OHBM meetings by selecting one of the following options:
I am submitting this abstract as an original work to be reproduced. I am available to be the “source party” in an upcoming team and consent to have this work listed on the OSSIG website. I agree to be contacted by OSSIG regarding the challenge and may share data used in this abstract with another team.
Please indicate below if your study was a "resting state" or "task-activation” study.
Resting state
Healthy subjects only or patients (note that patient studies may also involve healthy subjects):
Healthy subjects
Was this research conducted in the United States?
No
Were any human subjects research approved by the relevant Institutional Review Board or ethics panel?
NOTE: Any human subjects studies without IRB approval will be automatically rejected.
Yes
Were any animal research approved by the relevant IACUC or other animal research panel?
NOTE: Any animal studies without IACUC approval will be automatically rejected.
Not applicable
Please indicate which methods were used in your research:
Functional MRI
Structural MRI
For human MRI, what field strength scanner do you use?
3.0T
Which processing packages did you use for your study?
AFNI
SPM
FSL
Free Surfer
Provide references using APA citation style.
Burt, J. B., Demirtaş, M., Eckner, W. J., Navejar, N. M., Ji, J. L., Martin, W. J., Bernacchia, A., Anticevic, A., & Murray, J. D. (2018). Hierarchy of transcriptomic specialization across human cortex captured by structural neuroimaging topography. Nature Neuroscience, 21(9), Article 9. https://doi.org/10.1038/s41593-018-0195-0
Huntenburg, J. M., Bazin, P.-L., & Margulies, D. S. (2018). Large-Scale Gradients in Human Cortical Organization. Trends in Cognitive Sciences, 22(1), 21–31. https://doi.org/10.1016/j.tics.2017.11.002
Margulies, D. S., Ghosh, S. S., Goulas, A., Falkiewicz, M., Huntenburg, J. M., Langs, G., Bezgin, G., Eickhoff, S. B., Castellanos, F. X., Petrides, M., Jefferies, E., & Smallwood, J. (2016). Situating the default-mode network along a principal gradient of macroscale cortical organization. Proceedings of the National Academy of Sciences, 113(44), 12574–12579. https://doi.org/10.1073/pnas.1608282113
Paquola, C., Wael, R. V. D., Wagstyl, K., Bethlehem, R. A. I., Hong, S.-J., Seidlitz, J., Bullmore, E. T., Evans, A. C., Misic, B., Margulies, D. S., Smallwood, J., & Bernhardt, B. C. (2019). Microstructural and functional gradients are increasingly dissociated in transmodal cortices. PLOS Biology, 17(5), e3000284. https://doi.org/10.1371/journal.pbio.3000284
Sydnor, V. J., Larsen, B., Bassett, D. S., Alexander-Bloch, A., Fair, D. A., Liston, C., Mackey, A. P., Milham, M. P., Pines, A., Roalf, D. R., Seidlitz, J., Xu, T., Raznahan, A., & Satterthwaite, T. D. (2021). Neurodevelopment of the association cortices: Patterns, mechanisms, and implications for psychopathology. Neuron, 109(18), 2820–2846. https://doi.org/10.1016/j.neuron.2021.06.016
Wagstyl, K., Ronan, L., Goodyer, I. M., & Fletcher, P. C. (2015). Cortical thickness gradients in structural hierarchies. NeuroImage, 111, 241–250. https://doi.org/10.1016/j.neuroimage.2015.02.036
No