NiCHART: A Software Suite to Translate Neuroimaging Big Data to Individualized Biomarkers in Disease

Presented During:

Tuesday, June 25, 2024: 12:00 PM - 1:15 PM
COEX  
Room: Grand Ballroom 103  

Poster No:

2259 

Submission Type:

Abstract Submission 

Authors:

Fengling Hu1, Guray Erus1, George Aidinis1, Kyunglok Baik1, Matthew Cieslak1, Yuhan Cui1, Alexander Getka1, Hongming Li1, Yuncong Ma1, Zheng Ren1, Taylor Salo1, Dhivya Srinivasan1, Di Wu1, Mark Bergman1, Daniel Wolf1, Russell Shinohara1, Theodore Satterthwaite1, Haochang Shou1, Yong Fan1, Ilya Nasrallah1, Christos Davatzikos1

Institutions:

1University of Pennsylvania, Philadelphia, PA

First Author:

Fengling Hu  
University of Pennsylvania
Philadelphia, PA

Co-Author(s):

Guray Erus  
University of Pennsylvania
Philadelphia, PA
George Aidinis  
University of Pennsylvania
Philadelphia, PA
Kyunglok Baik  
University of Pennsylvania
Philadelphia, PA
Matthew Cieslak  
University of Pennsylvania
Philadelphia, PA
Yuhan Cui  
University of Pennsylvania
Philadelphia, PA
Alexander Getka  
University of Pennsylvania
Philadelphia, PA
Hongming Li  
University of Pennsylvania
Philadelphia, PA
Yuncong Ma  
University of Pennsylvania
Philadelphia, PA
Zheng Ren  
University of Pennsylvania
Philadelphia, PA
Taylor Salo  
University of Pennsylvania
Philadelphia, PA
Dhivya Srinivasan  
University of Pennsylvania
Philadelphia, PA
Di Wu  
University of Pennsylvania
Philadelphia, PA
Mark Bergman  
University of Pennsylvania
Philadelphia, PA
Daniel Wolf  
University of Pennsylvania
Philadelphia, PA
Russell Shinohara  
University of Pennsylvania
Philadelphia, PA
Theodore Satterthwaite  
University of Pennsylvania
Philadelphia, PA
Haochang Shou  
University of Pennsylvania
Philadelphia, PA
Yong Fan  
University of Pennsylvania
Philadelphia, PA
Ilya Nasrallah  
University of Pennsylvania
Philadelphia, PA
Christos Davatzikos  
University of Pennsylvania
Philadelphia, PA

Introduction:

Growing availability of open-access, large-scale neuroimaging data in healthy development and disease allows for rapid discovery of radiologic, neurologic, and psychiatric insights . This is especially true in the context of machine learning (ML), which promises improved prediction of diagnoses, prognoses, disease subtypes, and more. However, harnessing ML to pursue such precision medicine efforts remains a challenge for many neuroimaging scientists – barriers in coding skills, field-specific knowledge of state-of-the-art methodology, and access to large-scale neuroimaging data all limit the rate of biomarker discovery. We introduce niCHART (NeuroImaging Computational Harmonization and ARtificial intelligence Toolbox), a mutually-compatible ecosystem of state-of-the-art methods allowing for holistic processing of multi-modal MRI images as well as calculation of statistical and ML-based imaging-derived phenotypes (IDPs). Ultimately, niCHART will allow for improved reproducibility and accessibility of neuroimaging analysis as well as allow end-users to contextualize their own data among open-access, curated neuroimaging big data.

Methods:

niCHART integrates all-in-one software pipelines for pre-processing, harmonization, and statistical analysis of structural MRI, diffusion MRI, and functional MRI (Figure 1). Image pre-processing components consist of a validated structural MRI atlas-based segmentation pipeline, fMRIPrep, XCPEngine, QSIPrep (q-space image preprocesing), sopNMF (stochastic orthogonally projectie non-negative matrix factorization), and pNet (personalized networks) [1-7]. Post-processing components include generalized ComBat family harmonization methods, SPARE (Spatial Pattern of Abnormality for Recognition) IDP methods, smileGAN (SeMI-supervised cLustEring via Generative Adversarial Network), and more [8-12]. Additionally, niCHART develops a statistical and ML-based dimensional system based on a large reference population and automatically projects end-user image data into this dimensional system. These niCHART dimensions capture multivariate imaging patterns of brain heterogeneity covering both normative aging and disease.

Results:

niCHART reference data consists of pooled and harmonized multi-modal imaging data from 62,859 individuals across 24 studies (Figure 2). These reference individuals are demographically diverse with respect to age, sex, race, and underlying health conditions. Statistically-extracted IDPs include atlas-based anatomical and network segmentations, data-driven parcellations, structural covariance networks, and network metrics. In neurodegeneration, additional ML IDPs include deep learning metrics describing spatial patterns of atrophy related to normal aging, Alzheimer disease, and cardiovascular disease as well as metrics for subgroup identification within Alzheimer disease patients. In neuropsychiatry, ML IDPs include indices related to normal development, depression, autism spectrum disorder, and schizophrenia. Statistical harmonization models for IDPs have been pre-trained on this reference data and allow for automated harmonization of end-user data to the reference data, which allows for improved reproducibility and more valid inference.

Conclusions:

niCHART offers an accessible and feature-rich software suite for processing and analysis of neuroimaging data to translate state-of-the-art methodology to the individual-subject level. niCHART's panel of statistical and ML IDPs allow end-users to automatically extract high-level, individualized information from complex imaging data and contextualize their subjects among demographically and phenotypically diverse reference subjects. This machinery promises to accelerate research in precision medicine and dimensional phenomics.

Disorders of the Nervous System:

Neurodegenerative/ Late Life (eg. Parkinson’s, Alzheimer’s)

Lifespan Development:

Early life, Adolescence, Aging

Neuroinformatics and Data Sharing:

Databasing and Data Sharing 2
Workflows 1
Informatics Other

Keywords:

Aging
Data Organization
Degenerative Disease
Informatics
Machine Learning
MRI
Open Data
Open-Source Software
Statistical Methods
Workflows

1|2Indicates the priority used for review
Supporting Image: NiChart_Architecture_Simple.png
   ·Visualization of niCHART integrated software platform, including mutually-compatible web-based processing and local container-based pipelines.
Supporting Image: NiChart_OHBM.png
   ·Visualization of niCHART general analysis pipeline, post-processing data visualization, and ML-based dimensional representation system for biomarker discovery with inclusion of a reference data..
 

Provide references using author date format

[1] Tustison, N.J. 2021. The ANTsX ecosystem for quantitative biological and medical imaging. Sci Rep 11, 9068. https://doi.org/10.1038/s41598-021-87564-6
[2] Doshi, J. 2016. MUSE: MUlti-atlas region Segmentation utilizing Ensembles of registration algorithms and parameters, and locally optimal atlas selection. Neuroimage 127, 186–195. https://doi.org/10.1016/j.neuroimage.2015.11.073
[3] Esteban, O. 2019. fMRIPrep: a robust preprocessing pipeline for functional MRI. Nat Methods 16, 111–116. https://doi.org/10.1038/s41592-018-0235-4
[4] Ciric, R. 2017. Benchmarking of participant-level confound regression strategies for the control of motion artifact in studies of functional connectivity. Neuroimage 154, 174–187. https://doi.org/10.1016/j.neuroimage.2017.03.020
[5] Cieslak, M. 2021. QSIPrep: an integrative platform for preprocessing and reconstructing diffusion MRI data. Nat Methods 18, 775–778. https://doi.org/10.1038/s41592-021-01185-5
[6] Sotiras, A. 2015. Finding imaging patterns of structural covariance via Non-Negative Matrix Factorization. NeuroImage 108, 1–16. https://doi.org/10.1016/j.neuroimage.2014.11.045
[7] Li, H. 2017. Large-scale sparse functional networks from resting state fMRI. Neuroimage 156, 1–13. https://doi.org/10.1016/j.neuroimage.2017.05.004
[8] Pomponio, R. 2020. Harmonization of large MRI datasets for the analysis of brain imaging patterns throughout the lifespan. NeuroImage 208, 116450. https://doi.org/10.1016/j.neuroimage.2019.116450
[9] Chen, A.A. 2022. Mitigating site effects in covariance for machine learning in neuroimaging data. Hum Brain Mapp 43, 1179–1195. https://doi.org/10.1002/hbm.25688
[10] Davatzikos, C. 2009. Longitudinal progression of Alzheimer’s-like patterns of atrophy in normal older adults: the SPARE-AD index. Brain 132, 2026–2035. https://doi.org/10.1093/brain/awp091
[11] Habes, M. 2016. Advanced brain aging: relationship with epidemiologic and genetic risk factors, and overlap with Alzheimer disease atrophy patterns. Transl Psychiatry 6, e775. https://doi.org/10.1038/tp.2016.39
[12] Yang, Z. 2021. A deep learning framework identifies dimensional representations of Alzheimer’s Disease from brain structure. Nat Commun 12, 7065. https://doi.org/10.1038/s41467-021-26703-z