Effects of phase-encoding on BOLD data with a positive control task

Poster No:

1361 

Submission Type:

Abstract Submission 

Authors:

Céline Provins1, Alexandre Cionca1, Elodie Savary1, Patric Hagmann1, Oscar Esteban1

Institutions:

1Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland

First Author:

Céline Provins  
Lausanne University Hospital and University of Lausanne
Lausanne, Switzerland

Co-Author(s):

Alexandre Cionca  
Lausanne University Hospital and University of Lausanne
Lausanne, Switzerland
Elodie Savary  
Lausanne University Hospital and University of Lausanne
Lausanne, Switzerland
Patric Hagmann  
Lausanne University Hospital and University of Lausanne
Lausanne, Switzerland
Oscar Esteban  
Lausanne University Hospital and University of Lausanne
Lausanne, Switzerland

Introduction:

Quality assessment and quality control (QA/QC) checkpoints layered throughout the dataflow are essential to ensure the reliability of neuroimaging analyses (Niso et al. 2022). In the case of functional MRI, best practices recommend collecting a 'positive control' task with which the different layers of QA/QC can be validated. These are short and simple tasks designed to elicit robust and precisely located brain activation patterns, permitting the diagnosis of potential issues in the workflow. Here, we examine how the phase-encoding direction (PE) choice in echo-planar imaging (EPI) blood-oxygen-level-dependent (BOLD) fMRI influences the resulting activation maps using a positive control task that includes visual and motor paradigms.

Methods:

Data. 36 fMRI images were extracted from a dense sampling dataset, called the Human Connectome Phantom (HCPh), acquired as part of a registered report (Provins et al. 2023). A single male subject underwent repeated scans over four weeks. fMRI was acquired in a 3T Siemens Magnetom PrismaFit using a multi-echo EPI BOLD sequence varying PE across sessions in the four possible directions: anterior-posterior (AP), PA, left-right (LR), and RL. The echo times were TE=(12.60/33.04/53.48/73.92)ms. The other parameters, unchanged across sessions, were: 99 volumes with TR=1.6s, FA=64°, 2.2×2.2×2.2[mm3] resolution, distance factor 0%, 60 slices, 96×96 matrix, FOV=211mm, GRAPPA factor 2, SMS factor 4.
Task. Our quality control task (QCT), implemented with PsychoPy (Peirce et al. 2019), was adapted from the 'eye-movement' variant of the tasks proposed by (Harvey et al. 2018). It consists of four paradigms: a central fixation dot (blank), gaze movement, visual grating patterns, and a finger-tapping (left/right) block. The presentation order and realization of these paradigms (e.g. the coordinates in the gaze movement and the hand in fingertapping) were randomized.
Preprocessing. Data were preprocessed with fMRIPrep (Esteban et al. 2019) and further denoised by regressing out the 6 motion parameters, the WM and CSF mean signal, censoring frames with a framewise displacement above 0.4mm and smoothed to an estimated 4mm Gaussian kernel. No susceptibility distortion correction was applied to preserve the impact of different PE directions. Four QCT fMRI scans were excluded, three due to failed fMRIPrep runs and one for incorrectly defined events.
Task activation analysis. We used an event-based first-level model to estimate which voxels are significantly active during the tasks. Second-level models were then constructed using PE as confounds. The models were implemented with nilearn ("Nilearn" 2023).
Data & code availability. The HCPh dataset and the fMRIPrep derivatives will be publicly released with the Stage 2 culmination of the corresponding registered report. The task implementation is openly available at https://github.com/TheAxonLab/HCPh-fMRI-tasks. Our analysis is openly available as an educational notebook at https://www.axonlab.org/hcph-sops/analysis/qct-activation/.

Results:

Our QCT produces precisely-located brain activations. Confirming that the responses align with the expected activations is an integral component of the quality control protocol for our HCPh project (Figure 1).
Different PE caused activation disparities beyond susceptibility distortion-prone areas. We constrasted several pairs of PE and report the most relevant one in Figure 2. The latter highlights significant differences in fingertapping-induced activation within a segment of the primary motor cortex, a region that is usually not considered impacted by susceptibility distortion.
Supporting Image: QCTactivation_figure1.png
Supporting Image: QCTactivation_figure2.png
 

Conclusions:

Quality control tasks, acquired in just a few minutes, can easily be integrated into any acquisition protocol, serving as a potent tool to assess the integrity of analysis workflows. We showcased its potential by examining how PE affects task activation maps. Next steps include inspecting maps in subject space and further interpreting the differences among PE directions.

Modeling and Analysis Methods:

Activation (eg. BOLD task-fMRI) 1

Neuroinformatics and Data Sharing:

Workflows 2

Novel Imaging Acquisition Methods:

BOLD fMRI

Keywords:

Data analysis
Design and Analysis
FUNCTIONAL MRI
Modeling
Open Data
Open-Source Code
Open-Source Software
Pre-registration
Other - Quality Control; positive control task;

1|2Indicates the priority used for review

Provide references using author date format

Esteban, Oscar, Christopher J. Markiewicz, Ross W. Blair, Craig A. Moodie, A. Ilkay Isik, Asier Erramuzpe, James D. Kent, et al. 2019. “fMRIPrep: A Robust Preprocessing Pipeline for Functional MRI.” Nature Methods 16 (1): 111–16. https://doi.org/10.1038/s41592-018-0235-4.
Harvey, Jessica-Lily, Lysia Demetriou, John McGonigle, and Matthew B. Wall. 2018. “A Short, Robust Brain Activation Control Task Optimised for Pharmacological fMRI Studies.” PeerJ 6 (September): e5540. https://doi.org/10.7717/peerj.5540.
“Nilearn.” 2023. https://doi.org/10.5281/zenodo.8397157.
Niso, Guiomar, Rotem Botvinik-Nezer, Stefan Appelhoff, Alejandro De La Vega, Oscar Esteban, Joset A. Etzel, Karolina Finc, et al. 2022. “Open and Reproducible Neuroimaging: From Study Inception to Publication.” NeuroImage 263 (November): 119623. https://doi.org/10.1016/j.neuroimage.2022.119623.
Peirce, Jonathan, Jeremy R. Gray, Sol Simpson, Michael MacAskill, Richard Höchenberger, Hiroyuki Sogo, Erik Kastman, and Jonas Kristoffer Lindeløv. 2019. “PsychoPy2: Experiments in Behavior Made Easy.” Behavior Research Methods 51 (1): 195–203. https://doi.org/10.3758/s13428-018-01193-y.
Provins, Céline, Yasser Alemán-Gómez, Eleonora Fornari, Benedetta Franceschiello, Hélène Lajous, William H. Thompson, Ileana Jelescu, Patric Hagmann, and Oscar Esteban. 2023. “Reliability Characterization of MRI Measurements for Analyses of Brain Networks on a Human Phantom.” Nat. Methods (Stage 1 accepted-in-principle) https://doi.org/10.17605/OSF.IO/VAMQ6.