Evidence map›Paper›PMID 40384457›Full record

ArticleMagnetic resonance in medicine2025

MULti-TImepoint VElocity-selective Reconciled with Spatially-sElective (MULTIVERSE) ASL: Improving robustness to both shortened and prolonged arterial transit time.

Feng Xu, Dan Zhu, Dapeng Liu, Anja Soldan, Marilyn Albert, Martin A Lindquist, Doris D M Lin, Qin Qin

Abstract read
In one paragraph

Article in Magnetic resonance in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Feng XuThe Russell H. Morgan Department of Radiology and Radiological Science, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0001-7958-3787
Dan ZhuThe Russell H. Morgan Department of Radiology and Radiological Science, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0002-0940-1519
Dapeng LiuThe Russell H. Morgan Department of Radiology and Radiological Science, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0002-4432-3202
Anja SoldanDepartment of Neurology, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Marilyn AlbertDepartment of Neurology, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Martin A LindquistDepartment of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, USA.
Doris D M LinThe Russell H. Morgan Department of Radiology and Radiological Science, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Qin QinThe Russell H. Morgan Department of Radiology and Radiological Science, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0002-6432-2944

Funding

Research Education ComponentP30AG066507 · NIA · JOHNS HOPKINS UNIVERSITY · PI MARILYN S. ALBERT · 2020 to 2026
$29.3M
TRD 4: Platforms for multi-modal and multi-scale imaging dataP41EB031771 · NIBIB · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI Hanzhang Lu, Peter CM Van Zijl · 2021 to 2026
$9.9M
Velocity-Selective Arterial Spin Labeling based Perfusion Mapping for Alzheimer's diseaseRF1AG082243 · NIA · JOHNS HOPKINS UNIVERSITY · PI QIN, QIN · 2023 to 2023
$2.4M
Non-Contrast-Enhanced Velocity-Selective MR Angiography at 3T for Cerebrovascular DiseasesR01HL138182 · NHLBI · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI QIN, QIN · 2018 to 2022
$2.0M
Development and Evaluation of Advanced Non-Contrast Perfusion MRI for Monitoring Treatment Response in Brain MetastasesR01CA282928 · NCI · UNIVERSITY OF WASHINGTON · PI QIN, QIN · 2023 to 2025
$1.8M
Velocity-Selective Arterial Spin Labeling based Perfusion Mapping for Cerebrovascular DiseasesR01HL144751 · NHLBI · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI QIN, QIN · 2019 to 2022
$1.7M
Non-Contrast-Enhanced MRI for Brain Perfusion Mapping of Lewy Body DementiaR01NS139369 · NINDS · UNIVERSITY OF WASHINGTON · PI Dan Zhu · 2024 to 2026
$1.3M
Imaging Vascular Function in Normal Aging, MCI, and Mild DementiaK25AG083114 · NIA · JOHNS HOPKINS UNIVERSITY · PI Feng Xu · 2024 to 2026
$444k
Division of Cancer Prevention, National Cancer Institute CA282928National Heart and Lung Institute HL138182National Heart and Lung Institute HL144751NCI NIH HHS R01 CA282928NHLBI NIH HHS R01 HL138182NHLBI NIH HHS R01 HL144751NIA NIH HHS AG066507NIA NIH HHS AG082243NIA NIH HHS AG083114NIA NIH HHS K25 AG083114NIA NIH HHS P30 AG066507NIA NIH HHS RF1 AG082243NIBIB NIH HHS EB031771NIBIB NIH HHS P41 EB031771NINDS NIH HHS NS139369NINDS NIH HHS R01 NS139369
6 · The paper itself

Abstract

purposeTo improve the quantification of existing multi-timepoint arterial spin labeling (ASL) methods in estimating cerebral blood flow (CBF) and arterial transit time (ATT) for a wider range of ATTs.

methodsMULti-TImepoint VElocity-selective Reconciled with Spatially-sElective (MULTIVERSE) ASL utilizes multi-delay pseudo-continuous (PC) ASL and velocity-selective (VS) ASL with spatially defined bolus, and joint fitting to estimate CBF and ATT. Numerical simulations were performed to evaluate the accuracy and precision of single-delay and multi-delay PCASL and VSASL, as well as the proposed MULTIVERSE ASL, in quantifying CBF and ATT across an extended range of ATTs. The CBF and ATT estimates between multi-delay PCASL, VSASL, and MULTIVERSE ASL were compared across healthy volunteers.

resultsNumerical simulations showed that the utility of MULTIVERSE ASL improved the accuracy and precision over an extended ATT range of up to 4000 ms. In vivo scans from healthy subjects demonstrated that MULTIVERSE ASL led to reduced uncertainty in CBF and ATT quantification compared to multi-post-labeling delay PCASL while maintaining comparable repeatability.

conclusionThis novel and straightforward approach improves the accuracy and precision of the fitted CBF and ATT over an extended range of ATT, which is not possible with existing ASL methods. Brain scans from healthy subjects demonstrated the feasibility and reliability of the technique, highlighting the clinical potential of ASL-based perfusion mapping in various altered physiological and pathological conditions.

Indexed as

BrainCerebrovascular CirculationImage Processing, Computer-AssistedMagnetic Resonance AngiographyMagnetic Resonance ImagingAdultAlgorithmsBlood Flow VelocityComputer SimulationFemaleHealthy VolunteersHumansMaleReproducibility of ResultsSpin LabelsYoung AdultSpin Labelsarterial spin labeling (ASL)arterial transit time (ATT)bolus arrival time (BAT)bolus durationcerebral blood flowMULTIVERSE ASLpseudo‐continuous ASL (PCASL)velocity‐selective ASL (VSASL)

Identifiers

PMID40384457
PMCPMC12204808

What OpenQuestion holds

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Registered trials

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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.