Evidence map›Paper›PMID 41648381›Full record

ArticlebioRxiv : the preprint server for biology2026

Simultaneous Real-time Imaging of Neurofluid and Neurovascular Dynamics Using Ultrafast Flow-weighted Echo-Planar Imaging.

Amir H Shaker, Amir H G Arani, Bryn A Martin, Aristeidis Sotiras, Cihat Eldeniz, Helia Hosseini, Joshua S Shimony, David D Limbrick, Jennifer M Strahle, Arash Nazeri

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Amir H ShakerMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Amir H G AraniMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Bryn A MartinUniversity of Idaho, Department of Chemical and Biological Engineering, Moscow, ID.
Aristeidis SotirasMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Cihat EldenizMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Helia HosseiniMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Joshua S ShimonyMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
David D LimbrickDepartment of Pediatric Neurosurgery, Virginia Commonwealth University, Richmond, VA.
Jennifer M StrahleImaging Science Program, McKelvey School of Engineering, Washington University in St. Louis, St. Louis, MO.
Arash NazeriMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-6983-0641

Funding

Redefining Chiari Type I Malformation through Genetically, Radiologically, and Clinically-Derived Endophenotypes that are Predictive of Long-Term Neurological OutcomeP01NS131131 · NINDS · WASHINGTON UNIVERSITY · PI David Delmar Limbrick, Chenyang Lu · 2023 to 2026
$7.6M
NINDS NIH HHS P01 NS131131
6 · The paper itself

Abstract

Cerebrospinal fluid (CSF) circulation is tightly coupled to cerebral blood flow under the fixed-volume constraint of the cranial vault, with cardiac pulsations and respiration acting as dominant physiological drivers. Disruption of these flow dynamics has been implicated in various neurological disorders, motivating the need for imaging methods that capture CSF and vascular flow simultaneously and in real time. Conventional phase contrast MRI (PC-MRI) provides quantitative CSF velocity measurements but relies on cardiac gating and velocity encoding, which limit temporal resolution, dynamic range, and sensitivity to non-cardiac fluctuations. Here, we introduce self-gated ultrafast real-time flow-weighted echo-planar imaging (SURF-EPI), an inflow-weighted approach in which signal intensity reflects the replacement of saturated spins by freshly inflowing, unsaturated water molecules, yielding higher signal with higher flow. This allows simultaneous assessment of arterial inflow, venous outflow, and CSF motion at high temporal resolution. SURF-EPI was acquired at the C2-C3 spinal level, enabling real-time imaging of CSF flow dynamics in the cervical spinal canal alongside arterial and venous blood flow in major cervical vessels (frame-rate: 21.7 Hz). In addition to frequency-domain analyses, we leveraged intrinsic arterial signal fluctuations as a timing reference to reconstruct cardiac-resolved CSF dynamics for individual cardiac cycles without external physiological recordings. Frequency-domain analysis revealed distinct spectral signatures in CSF flow compared with neurovascular flow, including broadened cardiac peaks and enhanced respiratory modulation, particularly within the ventral spinal canal. In contrast, dorsal CSF showed increased power within the cardiac frequency band, higher coherence with cervical vasculature at the cardiac frequency, and reduced non-cardiac contributions. Time-domain analysis showed strong correlation between CSF flow waveforms derived from SURF-EPI and PC-MRI. Beyond ensemble-averaged waveforms, SURF-EPI enabled beat-to-beat analysis, revealing substantial cycle-to-cycle variability in CSF flow that is not captured by time-averaged gated approaches. Together, these findings establish SURF-EPI as a rapid, complementary framework to PC-MRI, enabling real-time neurofluid imaging with integrated time- and frequency-domain characterization of CSF and neurovascular flow dynamics.

Indexed as

CSF flowneurofluid imagingneurovascular imagingreal-time MRItemporal dynamics

Identifiers

PMID41648381
PMCPMC12871303

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.