ArticleNature communications2025
MR perfusion source mapping depicts venous territories and reveals perfusion modulation during neural activation.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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.
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.
Who cites it
3 citing papers in PubMed.
- Large-Vessel Venous Signal Confounds Apparent Amygdala Activation in BOLD fMRI.bioRxiv : the preprint server for biology · 2026Article
- Imaging Venous Transit Time and Blood-Brain Barrier Permeability of the Deep Brain.Magnetic resonance in medicine · 2026Article
- Bi-component modeling of cerebrospinal fluid outflow using Time-SLIP MRI.Fluids and barriers of the CNS · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
The cerebral venous system plays a crucial role in neurological and vascular conditions, yet its hemodynamics remain underexplored due to its complexity and variability across individuals. To address this, we develop a venous perfusion source mapping method using Displacement Spectrum MRI, a non-contrast technique that leverages blood water as an endogenous tracer. Our technique encodes spatial information into the magnetization of blood water spins during tagging and detects it once the tagged blood reaches the brain's surface, where the signal-to-noise ratio is 3-4 times higher. We resolve the sources of blood entering the imaging slice across short (10 ms) to long (3 s) evolution times, effectively capturing perfusion sources in reverse. This approach enables the measurement of slow venous blood flow, including potential contributions from capillary beds and surrounding tissue. We demonstrate perfusion source mapping in the superior cerebral veins, verify its sensitivity to global perfusion modulation induced by caffeine, and establish its specificity by showing repeatable local perfusion modulation during neural activation. From all blood within the imaging slice, our method localizes the portion originating from an activated region upstream.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.