A multimodal study of multiscale individual structural-connectivity-based parcellations

Poster No:

1647 

Submission Type:

Abstract Submission 

Authors:

Clément Langlet1, Denis Rivière1, Bastien Herlin1, Ivy Uszynski1, Cyril Poupon1, Jean-François Mangin1

Institutions:

1BAOBAB, NeuroSpin, Université Paris-Saclay, CNRS, CEA, Gif-sur-Yvette, France

First Author:

Clément Langlet  
BAOBAB, NeuroSpin, Université Paris-Saclay, CNRS, CEA
Gif-sur-Yvette, France

Co-Author(s):

Denis Rivière  
BAOBAB, NeuroSpin, Université Paris-Saclay, CNRS, CEA
Gif-sur-Yvette, France
Bastien Herlin  
BAOBAB, NeuroSpin, Université Paris-Saclay, CNRS, CEA
Gif-sur-Yvette, France
Ivy Uszynski  
BAOBAB, NeuroSpin, Université Paris-Saclay, CNRS, CEA
Gif-sur-Yvette, France
Cyril Poupon  
BAOBAB, NeuroSpin, Université Paris-Saclay, CNRS, CEA
Gif-sur-Yvette, France
Jean-François Mangin  
BAOBAB, NeuroSpin, Université Paris-Saclay, CNRS, CEA
Gif-sur-Yvette, France

Introduction:

Mapping the brain is a long standing goal of the neuroscience community as cerebral maps provide a spatial referential crucial to understand the human brain. An additional application of these cerebral maps is the dimension reduction that they provide for further genetics and machine learning analyses. Two main strategies coexist to yield these maps: defining anatomical atlases or generating data-driven parcellations. However, these maps are often average templates that are projected onto the individual via an alignment driven by cortical landmarks, and fail to represent the anatomical peculiarities of the individuals (Glasser, 2016) (Mangin, 2019). Individual parcellations have already been shown to improve the study of cortical thickness heritability in some regions of the brain (Langlet, 2024), yet a better understanding across other phenotypes remains of interest for the brain mapping community. In this work, we generated multiscale individual parcellations using a data-driven algorithm based on structural connectivity profiles and studied their relevance using multimodal MRI data.

Methods:

First, we used a group-based clustering algorithm - Constellation (Lefranc and Roca, 2015) - to generate averaged subdivisions of the Desikan atlas (Desikan, 2006) based on structural connectivity profiles derived from the diffusion MRI of the HCP dataset (Van Essen, 2013) [Figure 1]. In each region, from 2 to 12 subdivisions were generated. These multiscale subdivisions were then projected onto 1004 subjects of the dataset using their individual structural connectivity profiles (Langlet, 2023). We then estimated the probability density function of each parcel - using a gaussian Kernel Density Estimation - on various phenotypes such as myelin, cortical thickness and cortical thickness corrected by curvature, grey matter volume, DTI measures (Fractional Anisotropy and Mean Diffusivity) and NODDI model (Zhang, 2012) indexes (Neurite Density Index and Orientation Dispersion Index). To study the impact of the number of subdivisions for each Desikan region and each modality, we used a Generalized Contrast-to-Noise ratio (gCNR) (Rodriguez-Molares, 2020) defined as an inverse function of the overlap between each subdivision and the neighbouring parcels. This process was applied on tractograms stemming from the FSL probabilistic tractography algorithm and the MRtrix algorithm using SIFT2 yielding two sets of results.
Supporting Image: constellation.png
   ·Constellation algorithm
 

Results:

We obtained the gCNR for multiscale subdivisions of Desikan regions for each studied phenotype and two tractography algorithms. Although the evolution of this score seems to follow a general trend across the number of subdivisions (kmax), it can be different according to the phenotype [Figure 2]. The evolution of the contrast score is fairly reproducible between the two tractography algorithms. These results suggest that, from a data processing point of view, there may be no such thing as one relevant number of parcels and this may depend on several factors such as the phenotype or the region of the brain.
Supporting Image: gcnr.png
   ·Generalized Contrast-to-Noise ratio on multiple phenotypes
 

Conclusions:

The present study gives insights into the relevance of individual parcellations for data processing purposes through a multimodal evaluation. Although the generalized Contrast-to-Noise ratio is not a standard score in the MRI community to study parcellations, the recent use of probability density estimates in MIND networks (Sebenius, 2023) has yielded promising results, therefore further investigations on the multiscale individual parcellations will be conducted. These multiscale individual parcellations will be provided to the community for replication and further studies.

Modeling and Analysis Methods:

Segmentation and Parcellation 1
Univariate Modeling 2

Keywords:

Data analysis
Morphometrics
MRI
Statistical Methods
STRUCTURAL MRI
Tractography
Univariate
White Matter
Other - Parcellations, Connectivity

1|2Indicates the priority used for review

Abstract Information

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Please indicate below if your study was a "resting state" or "task-activation” study.

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Healthy subjects only or patients (note that patient studies may also involve healthy subjects):

Healthy subjects

Was this research conducted in the United States?

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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.

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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.

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Please indicate which methods were used in your research:

Structural MRI
Diffusion MRI

For human MRI, what field strength scanner do you use?

3.0T

Which processing packages did you use for your study?

FSL
Free Surfer
Other, Please list  -   MRtrix, Brainvisa

Provide references using APA citation style.

Desikan, R. S. (2006). An automated labeling system for subdividing
the human cerebral cortex on mri scans into gyral based regions of interest.
NeuroImage, 31.

Glasser, M. F. (2016). A multi-modal parcellation of human cerebral cortex. Nature, 536(7615):171–178.

Langlet, C. (2023). Nested parcellations connectome delivered for one large dataset using constellation algorithm (v1.2).

Langlet, C. (2024). "Structural-Connectivity-Based Individual Parcellations Improve Regional Cortical Thickness Heritability Study," 2024 IEEE International Symposium on Biomedical Imaging (ISBI), Athens, Greece, 2024, pp. 1-5, doi: 10.1109/ISBI56570.2024.10635119.

Lefranc, S. and Roca, P. (2016). Groupwise connectivity-based parcellation of the whole human cortical surface using watershed-driven dimension reduction. Medical Image Analysis, 30.

Mangin, J.-F. (2019). “Plis de passage” Deserve a role in models of the cortical folding process. Brain Topography, 32.

Rodriguez-Molares A. (2020). The Generalized Contrast-to-Noise Ratio: A Formal Definition for Lesion Detectability. IEEE Trans Ultrason Ferroelectr Freq Control. 2020 Apr;67(4):745-759. doi: 10.1109/TUFFC.2019.2956855

Sebenius, I. (2023). Robust estimation of cortical similarity networks from brain MRI. Nat Neurosci 26, 1461–1471 (2023). https://doi.org/10.1038/s41593-023-01376-7

Van Essen, D. C. (2013). The WU-Minn Human Connectome Project: An overview. NeuroImage, 80:62–79.

Zhang H. (2012). NODDI: practical in vivo neurite orientation dispersion and density imaging of the human brain. Neuroimage. 2012 Jul 16;61(4):1000-16. doi: 10.1016/j.neuroimage.2012.03.072.

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