Anna K Mueller1, Miriam Heynckes2, Christopher J Wiggins3, Omer Faruk Gulban4, Yuhui Chai5, Benedikt Poser2, and Renzo Huber2
1Goethe-Universität Frankfurt am Main, Mainz, Germany, 2Faculty of Psychology and Neuroscience, Maastricht University, Maastricht, Netherlands, 3Scannexus, Maastricht, Netherlands, 4Brain Innovation, Maastricht, Netherlands, 5NIH, Bethesda, MD, United States
Synopsis
Laminar-specific fMRI allows neuroscientists to address research questions of directional functional connectivity within and across brain areas. While recent sequence developments allow considerable improvements in coverage, resolution, and mitigation of venous biases, it is not established how routinely useful those methods are for everyday neuroscientific application.
We present an open dataset of whole-brain CBV-sensitive layer-dependent fMRI during free movie watching. Its purpose is to:
- investigate the reproducibility of laminar connectivity results,
- to benchmark preprocessing pipelines,
- to provide reference atlases of laminar connectivity and venous physiology,
- and to explore new potential neuroscientific research questions that become addressable with laminar fMRI.
Purpose
Laminar-specific fMRI allows neuroscientists to address research questions of directional functional connectivity within and across brain areas. While recent sequence developments allow considerable improvements in coverage, resolution, and mitigation of venous biases, it is not established how usable those methods are for routine neuroscience praxis.
Here, we provide a whole-brain layer-dependent functional connectome dataset with cerebral blood volume and BOLD contrast. The purpose of this dataset is to:
- characterize the challenges of whole brain layer-fMRI acquisition sequences in a test-retest setting and to see which neuroscientific research questions are reliably addressable and which ones aren’t.
- provide a test bed for developing and benchmarking new layer-dependent preprocessing and analysis tools.
- provide an atlas of laminar connectivity and depth-specific vascular physiology (vascular reactivity).
- characterize the layer-dependent representation content across all areas.
Methods
Scanning was performed on a SIEMENS MAGNETOM “Classic” 7T scanner while subjects were watching the Human Connectome Project (HCP) audio movie. For layer-fMRI scanning without venous biases, a blood volume sensitive VASO (Lu 2003) sequence was used. We further developed a previously presented MAGEC VASO variant with an inversion T1-primer to increase the coverage by another 20% compared to previous protocols (Huber 2020).
Scanning: Resolution = 0.8mm iso, TR = 8.9s, 3D-EPI readout (Poser 2010), in-plane GRAPPA 3, TA = 14 min, 4-5 runs per session and 6 sessions in total (one of which failed). For further acquisition parameters see: https://github.com/layerfMRI/Sequence_Github/blob/master/Whole_brain_layers/Ann_WB_VASO_fMRI.pdf. Respiration and pulse traces were recorded to provide the required physiological measures for further analysis.
Data processing: Motion correction and VASO's BOLD correction was performed in LayNii. Segmentation of GM and WM were initially performed in BrainVoyager and then manually corrected. To estimate the functional sensitivity to extract brain networks, ICA was used and the number of ‘neural’ vs. ‘non-neural’ were counted for various layer-specific smoothing strengths.
Venous baseline CBV was extracted by means of the recorded respiratory volume using the VasA approach (Kazan 2017; Guidi 2020).
The data are openly accessible on OpenNeurio: https://10.18112/openneuro.ds003216.v1.0.0. We are happy to share the used sequence via SIEMENS C2P.Results and Discussion
Figs. 1 and 2 show that common acquisition and analysis procedures that work for conventional resolutions and small FOV laminar fMRI do not suffice for whole brain laminar fMRI. With the long EPI echo spacing (low bandwidth), which is necessary with the large matrix sizes, the common rigid body motion-correction across runs and sessions does not provide sufficient local accuracy. Higher-order non-linear motion correction with ANTs SyN (Avants 2008) becomes necessary. Furthermore, the small bandwidth also makes the data more sensitive to frequency drifts that cause run-consistent traveling-wave artifacts into the time series (Fig. 2), which suggests that laminar-fMRI results need to go though additional temporally shifted detrending (nuisance regression) steps.
Fig. 3 shows that the commonly low SNR of laminar fMRI can be accounted for with moderate layer-specific smoothing (Blazejewska 2019), without significantly reducing the laminar specificity.
Fig. 4 depicts a representative atlas of area specific distributions of vascular reactivity (venous baseline blood density) across depth. This atlas will play an important role in future studies using laminar signal models (Markuerkiaga 2016,2020; Havlicek 2019).
Fig. 5 depicts an exploratory analysis method to map brain areas based on their layer-specific information content. The purpose of this figure is to exemplify what kind of new research questions can be addressed with whole brain layer-fMRI datasets like this one that cannot be easily addressed with conventional fMRI protocols. Here we use it for hypothesis testing of two models of brain function: A representational vs. an intentional framework (Shadlen 2013). Conventional two-dimensional brain cartography often operates under the implicit assumption that each brain module's purpose is to ‘represent’ and ‘classify’ features and objects of the outside world. Laminar fMRI allows us to investigate how appropriate this model is. We find indeed that many associative areas seem to be also well characterized based on a ‘non-representational’, but by an ‘intentional’ framework (Shadlen 2013).Summary and Conclusion
Here we present an open dataset for benchmarking laminar fMRI acquisition, for testing and optimizing preprocessing strategies, and for characterizing the reproducibility of layer-fMRI neuroscience results. We find that upon appropriate preprocessing, common connectivity networks can be reliably obtained with local specificity to the laminar profiles. The exceptionally high number of identical runs in this dataset allow us to provide representational atlases of venous baseline blood volume distribution.
These data were further used to estimate a ‘column-by-column’ level characterization of whether or not a brain area is dominated from externally-driven feedforward activity or intentionally-driven endogenious activity. Acknowledgements
Help with scanning: These data were acquired with the kind support of scannexus at their 7T MAGENTOM “Classic” SIEMENS scanner. We thank Sebastian Dresbach and Kabir Arora for assistance with after hour scans. We thank Bianka Linssen for advice regarding head stabilization cushions and cardio-respiratory tracing.
Funding:
Anna Katharina Mueller was supported for this project by a fellowship from the Goethe-University in Frankfurt am Main.
Laurentius Huber was funded form the NWO VENI project 016.Veni.198.032.
Benedikt Poser is partially funded by the NWO VIDI grant 16.Vidi.178.052 and by the National Institute for Health grant (R01MH/111444) (PI David Feinberg).
Miriam Heynckes is funded by The Netherlands Organization for Scientific Research (NWO) Research Talent Grant 406.17.200.
Ethics: The scanning procedures have been approved by the Ethics Review Committee for Psychology and Neuroscience (ERCPN) at Maastricht University, following the principles expressed in the Declaration of Helsinki.
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