Evidence map›Paper›PMID 41253701›Full record

ArticleJournal of magnetic resonance imaging : JMRI2026

T2-Weighted T1 Mapping and Automated Segmentation of CSF: Assessment of Solute Gradients in the Healthy Brain.

Tryggve Holck Storås, Sofie Lysholm Lian, Ingrid Mossige, Jørgen Riseth, Siri Fløgstad Svensson, Grethe Løvland, Geir Ringstad, Kent-André Mardal, Kyrre Eeg Emblem, Kaja Nordengen

Abstract read
In one paragraph

Article in Journal of magnetic resonance imaging : JMRI, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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.

Tryggve Holck StoråsDepartment of Physics and Computational Radiology, Division of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway.ORCID 0009-0006-5359-4801
Sofie Lysholm LianInstitute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
Ingrid MossigeDepartment of Physics and Computational Radiology, Division of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway.
Jørgen RisethScientific Computing and Numerical Analysis (SCAN), Simula Research Laboratory, Oslo, Norway.
Siri Fløgstad SvenssonDepartment of Physics and Computational Radiology, Division of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway.
Grethe LøvlandThe Intervention Center, Oslo University Hospital, Oslo, Norway.ORCID 0000-0002-1866-9613
Geir RingstadInstitute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0003-0919-4510
Kent-André MardalKG Jebsen Center for Brain Fluid Research, UiO, Oslo, Norway.
Kyrre Eeg EmblemDepartment of Physics and Computational Radiology, Division of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway.
Kaja NordengenInstitute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0002-5897-6394

Funding

European Research Council 101141807HORIZON-MSCA-2023-DN-01 101169519Norwegian Health Association 25598Norwegian Research Council 333956South-Eastern Norway Health Authorities 2022022South-Eastern Norway Health Authorities 2023050Stiftelsen Kristian Gerhard Jebsen
6 · The paper itself

Abstract

backgroundCerebrospinal fluid (CSF) serves as a medium for nutrient delivery and waste clearance. The T1 relaxation rate, R1, can be used to measure the concentration of intrinsic solutes and extrinsic contrast agents. PURPOSE: To implement a method for R1 mapping and segmentation of CSF and to use this method to explore how R1 of CSF relates to protein content and gadobutrol after intrathecal administration. STUDY TYPE: Prospective cohort study, complemented by phantom analysis. POPULATION: Ten healthy control subjects (mean age 65.5 ± 4.4 years, range 57-72 years; five males and five females) and protein- and gadobutrol-gradient phantom. FIELD STRENGTH/SEQUENCE: 3 T Philips Ingenia scanner; 3D T2W mixed inversion recovery spin-echo (T2W-mixed IRSE) sequence and 3D T1W turbo field echo (3D T1W-TFE). ASSESSMENT: R1 maps were calculated by combining IR and SE data. An automated segmentation method derived from FreeSurfer employed SE data for CSF segmentation and T1W-TFE for anatomical reference. CSF was collected by lumbar puncture for protein measurements, and 0.25 mmol gadobutrol was injected intrathecally. Post-contrast assessments were performed at 3, 24, 48, and 72 h. STATISTICAL TESTS: One-way ANOVA, followed by a post hoc Tukey HSD test, and simple and multiple linear regression analysis; significance level of 0.05.

resultsR1 of ventricular CSF 0.216 ± 0.001 s DATA

conclusionIntrinsic R1 of CSF in the subarachnoid space correlated with protein content. Intracranial CSF enrichment after intrathecal administration of gadobutrol showed a large variation among healthy volunteers. EVIDENCE LEVEL: 2. TECHNICAL EFFICACY: 3.

Indexed as

BrainCerebrospinal FluidImage Processing, Computer-AssistedMagnetic Resonance ImagingAgedContrast MediaFemaleHumansImaging, Three-DimensionalMaleMiddle AgedOrganometallic CompoundsPhantoms, ImagingProspective StudiesContrast MediagadobutrolOrganometallic Compoundsautomated segmentationcerebrospinal fluid (CSF)gadolinium‐based contrast agents (GBCA)mixed MRI sequenceprotein clearancesubarachnoid space (SAS)

Identifiers

PMID41253701
PMCPMC13254029

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.