Evidence map›Paper›PMID 32141655›Full record

ArticleMagnetic resonance in medicine2020

Systematic evaluation of velocity-selective arterial spin labeling settings for placental perfusion measurement.

Anita A Harteveld, Jana Hutter, Suzanne L Franklin, Laurence H Jackson, Mary Rutherford, Joseph V Hajnal, Matthias J P van Osch, Clemens Bos, Enrico De Vita

Abstract read
In one paragraph

Article in Magnetic resonance in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  16. Fetal Neuroimaging Updates.Magnetic resonance imaging clinics of North America · 2021
    Review
  17. Article
  18. 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

9 authors.

Anita A HarteveldDepartment of Radiology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID 0000-0002-3379-0710
Jana HutterBiomedical Engineering, School of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom.ORCID 0000-0003-3476-3500
Suzanne L FranklinDepartment of Radiology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID 0000-0001-6886-5578
Laurence H JacksonBiomedical Engineering, School of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom.ORCID 0000-0002-5904-8012
Mary RutherfordBiomedical Engineering, School of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom.
Joseph V HajnalBiomedical Engineering, School of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom.
Matthias J P van OschC.J. Gorter Center for high field MRI, Department of Radiology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0001-7034-8959
Clemens BosDepartment of Radiology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Enrico De VitaBiomedical Engineering, School of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom.

Funding

Structure and function of the placenta from implantation to delivery: a next generation MRI approachU01HD087202 · NICHD · KING'S COLLEGE LONDON · PI ALEXANDER, DANIEL, ALJABAR, PAUL · 2015 to 2015
$3.2M
NICHD NIH HHS U01 HD087202Wellcome TrustWellcome Trust 201374/Z/16/ZWellcome Trust WT 203148/Z/16/Z
6 · The paper itself

Abstract

purposePlacental function is key for successful human pregnancies. Perfusion may be a sensitive marker for the in vivo assessment of placental function. Arterial spin labeling (ASL) MRI enables noninvasive measurement of tissue perfusion and it was recently suggested that ASL with velocity-selective (VS) labeling could be advantageous in the placenta. We systematically evaluated essential VS-ASL sequence parameters to determine optimal settings for efficient placental perfusion measurements.

methodsEleven pregnant women were scanned at 3T using VS-ASL with 2D multislice echo planar imaging (EPI)-readout. One reference VS-ASL scan was acquired in all subjects; within subgroups the following parameters were systematically varied: cutoff velocity, velocity encoding direction, and inflow time. Visual evaluation and region of interest analyses were performed to compare perfusion signal differences between acquisitions.

resultsIn all subjects, a perfusion pattern with clear hyperintense focal regions was observed. Perfusion signal decreased with inflow time and cutoff velocity. Subject-specific dependence on velocity encoding direction was observed. High temporal signal-to-noise ratios with high contrast on the perfusion images between the hyperintense regions and placental tissue were seen at ~1.6 cm/s cutoff velocity and ~1000 ms inflow time. Evaluation of measurements at multiple inflow times revealed differences in blood flow dynamics between placental regions.

conclusionPlacental perfusion measurements are feasible at 3T using VS-ASL with 2D multislice EPI-readout. A clear dependence of perfusion signal on VS labeling parameters and inflow time was demonstrated. Whereas multiple parameter combinations may advance the interpretation of placental circulation dynamics, this study provides a basis to select an effective set of parameters for the observation of placenta perfusion natural history and its potential pathological changes.

Indexed as

ArteriesMagnetic Resonance ImagingCerebrovascular CirculationFemaleHumansMagnetic Resonance AngiographyPerfusionPlacentaPregnancySpin LabelsSpin Labelsarterial spin labeling (ASL)magnetic resonance imagingperfusionplacental functionvelocity-selective arterial spin labeling

Identifiers

PMID32141655
PMCPMC7384055

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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.