Evidence map›Paper›PMID 31362150›Full record

ArticleNeuroImage. Clinical2019

Changes in brain perfusion in successive arterial spin labeling MRI scans in neonates with hypoxic-ischemic encephalopathy.

Maïa Proisy, Isabelle Corouge, Antoine Legouhy, Amélie Nicolas, Valérie Charon, Nadia Mazille, Stéphanie Leroux, Bertrand Bruneau, Christian Barillot, Jean-Christophe Ferré

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
6.2field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

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  19. Bedside and laboratory neuromonitoring in neonatal encephalopathy.Seminars in fetal & neonatal medicine · 2021
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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 at 2 institutions in 1 country.

Maïa ProisyUniv Rennes, Inria, CNRS, INSERM, IRISA, Empenn ERL U-1228, F-35000 Rennes, France; CHU Rennes, Radiology Department, F-35033 Rennes, France. Electronic address: maia.proisy@chu-rennes.fr.
Isabelle CorougeUniv Rennes, Inria, CNRS, INSERM, IRISA, Empenn ERL U-1228, F-35000 Rennes, France.
Antoine LegouhyUniv Rennes, Inria, CNRS, INSERM, IRISA, Empenn ERL U-1228, F-35000 Rennes, France.
Amélie NicolasCHU Rennes, Radiology Department, F-35033 Rennes, France.
Valérie CharonCHU Rennes, Radiology Department, F-35033 Rennes, France.
Nadia MazilleCHU Rennes, Neonatology Department, F-35033 Rennes, France.
Stéphanie LerouxCHU Rennes, Neonatology Department, F-35033 Rennes, France.
Bertrand BruneauCHU Rennes, Radiology Department, F-35033 Rennes, France.
Christian BarillotUniv Rennes, Inria, CNRS, INSERM, IRISA, Empenn ERL U-1228, F-35000 Rennes, France.
Jean-Christophe FerréUniv Rennes, Inria, CNRS, INSERM, IRISA, Empenn ERL U-1228, F-35000 Rennes, France; CHU Rennes, Radiology Department, F-35033 Rennes, France.
Centre Hospitalier Universitaire de Rennes · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The primary objective of this study was to evaluate changes in cerebral blood flow (CBF) using arterial spin labeling MRI between day 4 of life (DOL4) and day 11 of life (DOL11) in neonates with hypoxic-ischemic encephalopathy (HIE) treated with hypothermia. The secondary objectives were to compare CBF values between the different regions of interest (ROIs) and between infants with ischemic lesions on MRI and infants with normal MRI findings. We prospectively included all consecutive neonates with HIE admitted to the neonatal intensive care unit of our institution who were eligible for therapeutic hypothermia. Each neonate systematically underwent two MRI examinations as close as possible to day 4 (early MRI) and day 11 (late MRI) of life. A custom processing pipeline of morphological and perfusion imaging data adapted to neonates was developed to perform automated ROI analysis. Twenty-eight neonates were included in the study between April 2015 and December 2017. There were 16 boys and 12 girls. Statistical analysis was finally performed on 37 MRIs, 17 early MRIs and 20 late MRIs. Eleven neonates had both early and late MRIs of good quality available. Eight out of 17 neonates (47%) had an abnormal on late MRI as performed and 7/20 neonates (35%) had an abnormal late MRI. CBF values in the basal ganglia and thalami (BGT) and temporal lobes were significantly higher on DOL4 than on DOL11. There were no significant differences between DOL4 and DOL11 for the other ROIs. CBF values were significantly higher in the BGT vs. the cortical GM, on both DOL4 and DOL11. On DOL4, the CBF was significantly higher in the cortical GM, the BGT, and the frontal and parietal lobes in subjects with an abnormal MRI compared to those with a normal MRI. On DOL11, CBF values in each ROI were not significantly different between the normal MRI group and the abnormal MRI group, except for the temporal lobes. This article proposes an innovative processing pipeline for morphological and ASL data suited to neonates that enable automated segmentation to obtain CBF values over ROIs. We evaluate CBF on two successive scans within the first 15 days of life in the same subjects. ASL imaging in asphyxiated neonates seems more relevant when used relatively early, in the first days of life. The correlation of intra-subject changes in cerebral perfusion between early and late MRI with neurodevelopmental outcome warrants investigation in a larger cohort, to determine whether the CBF pattern change can provide prognostic information beyond that provided by visible structural abnormalities on conventional MRI.

Indexed as

Spin LabelsCerebrovascular CirculationCohort StudiesFemaleHumansHypoxia-Ischemia, BrainInfant, NewbornMagnetic Resonance ImagingMaleProspective StudiesSpin LabelsASLAsphyxiaCerebral perfusionMRINeonates

Identifiers

PMID31362150
PMCPMC6664197
OpenAlexW2957648308

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.