Evidence map›Paper›PMID 37768433›Full record

ArticleMagma (New York, N.Y.)2024

Subject-specific timing adaption in time-encoded arterial spin labeling imaging.

Nora-Josefin Breutigam, Daniel Christopher Hoinkiss, Simon Konstandin, Mareike Alicja Buck, Amnah Mahroo, Klaus Eickel, Federico von Samson-Himmelstjerna, Matthias Günther

Open access · hybridAbstract read
In one paragraph

Article in Magma (New York, N.Y.), 2024. 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
0.2field-weighted citation impact, top 40% of its field
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 citations in OpenAlex.

  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 at 4 institutions in 1 country.

Nora-Josefin BreutigamImaging Physics, Fraunhofer Institute for Digital Medicine MEVIS, Max-von-Laue-Str. 2, 28359, Bremen, Germany. nora-josefin.breutigam@mevis.fraunhofer.de.ORCID http://orcid.org/0000-0002-8528-9792
Daniel Christopher HoinkissImaging Physics, Fraunhofer Institute for Digital Medicine MEVIS, Max-von-Laue-Str. 2, 28359, Bremen, Germany.
Simon KonstandinImaging Physics, Fraunhofer Institute for Digital Medicine MEVIS, Max-von-Laue-Str. 2, 28359, Bremen, Germany.
Mareike Alicja BuckImaging Physics, Fraunhofer Institute for Digital Medicine MEVIS, Max-von-Laue-Str. 2, 28359, Bremen, Germany.
Amnah MahrooImaging Physics, Fraunhofer Institute for Digital Medicine MEVIS, Max-von-Laue-Str. 2, 28359, Bremen, Germany.
Klaus EickelImaging Physics, Fraunhofer Institute for Digital Medicine MEVIS, Max-von-Laue-Str. 2, 28359, Bremen, Germany.
Federico von Samson-HimmelstjernaImaging Physics, Fraunhofer Institute for Digital Medicine MEVIS, Max-von-Laue-Str. 2, 28359, Bremen, Germany.
Matthias GüntherImaging Physics, Fraunhofer Institute for Digital Medicine MEVIS, Max-von-Laue-Str. 2, 28359, Bremen, Germany.
Fraunhofer Institute for Digital Medicine · DEUniversity of Bremen · DEHochschule Bremerhaven · DEMediri (Germany) · DE

Funding

EU Joint Programme - Neurodegenerative Disease Research 825664
6 · The paper itself

Abstract

objectivesOne challenge in arterial spin labeling (ASL) is the high variability of arterial transit times (ATT), which causes associated arterial transit delay (ATD) artifacts. In patients with pathological changes, these artifacts occur when post-labeling delay (PLD) and bolus durations are not optimally matched to the subject, resulting in difficult quantification of cerebral blood flow (CBF) and ATT. This is also true for the free lunch approach in Hadamard-encoded pseudocontinuous ASL (H-pCASL). MATERIAL AND

methodsFive healthy volunteers were scanned with a 3 T MR-system. pCASL-subbolus timing was adjusted individually by the developed adaptive Walsh-ordered pCASL sequence and an automatic feedback algorithm. The quantification results for CBF and ATT and the respective standard deviations were compared with results obtained using recommended timings and intentionally suboptimal timings.

resultsThe algorithm individually adjusted the pCASL-subbolus PLD for each subject within the range of recommended timing for healthy subjects, with a mean intra-subject adjustment deviation of 47.15 ms for single-shot and 44.5 ms for segmented acquisition in three repetitions. DISCUSSION: A first positive assessment of the results was performed on healthy volunteers. The extent to which the results can be transferred to patients and are of benefit must be investigated in follow-up studies.

Indexed as

ArteriesMagnetic Resonance ImagingCerebrovascular CirculationHumansReproducibility of ResultsSpin LabelsSpin LabelsArterial spin labelingArterial transit delay artifactsFree-lunch approachSubject-specific timingTime-encoded pCASL

Identifiers

PMID37768433
PMCPMC10876770
OpenAlexW4387115860

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.