Evidence map›Paper›PMID 37419079›Full record

ArticleEarly human development2023

Evaluation of neurovascular coupling during neuroprotective therapies: A single site HEAL ancillary study.

Lina F Chalak, Shu Kang, Srinivas Kota, Hanli Liu, Yulun Liu, Sandra E Juul, Yvonne W Wu

Open access · greenAbstract read
In one paragraph

Article in Early human development, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

7 authors at 5 institutions in 1 country.

Lina F ChalakDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX, United States of America. Electronic address: Lina.chalak@utsouthwestern.edu.
Shu KangDepartment of Bioengineering, University of Texas at Arlington, Arlington, TX, United States of America.
Srinivas KotaDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX, United States of America.
Hanli LiuDepartment of Bioengineering, University of Texas at Arlington, Arlington, TX, United States of America.
Yulun LiuDepartment of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, United States of America.
Sandra E JuulDivision of Neonatology, Department of Pediatrics, University of Washington School of Medicine, Seattle, WA, United States of America.
Yvonne W WuDepartment of Neurology, University of California San Francisco, San Francisco, CA, United States of America.
The University of Texas at Arlington · USThe University of Texas Southwestern Medical Center · USSouthwestern Medical Center · USUniversity of California, San Francisco · USUniversity of Washington · US

Funding

High-dose Erythropoietin for Asphyxia and Encephalopathy (HEAL) CCCU01NS092764 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JUUL, SANDRA E, WU, YVONNE W · 2016 to 2020
$12.7M
Mechanisms of Brain Dysmorphology in MN1 C-Terminal Truncation Syndrome, a Novel Intellectual Developmental Disability Disorder P50HD103524 · NICHD · UNIVERSITY OF WASHINGTON · PI Sandra E Juul · 2020 to 2026
$9.9M
A Novel Wavelet Neurovascular Bundle for Real Time Detection of Injury in Neonatal EncephalopathyR01NS102617 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI LINA F CHALAK · 2017 to 2026
$4.0M
NICHD NIH HHS P50 HD103524NINDS NIH HHS R01 NS102617NINDS NIH HHS U01 NS092764
6 · The paper itself

Abstract

backgroundThere is a critical need for development of physiological biomarkers in infants with birth asphyxia to identify the physiologic response to therapies in real time. This is an ancillary single site study of the High-Dose Erythropoietin for Asphyxia and Encephalopathy (Wu et al., 2022 [1]) to measure neurovascular coupling (NVC) non-invasively during an ongoing blinded randomized trial.

methodsNeonates who randomized in the HEAL enrolled at a single-center Level III Neonatal Intensive Care Unit were recruited between 2017 and 2019. Neurodevelopmental impairment was blinded and defined as any of the following: cognitive score <90 on Bayley Scales of Infant Toddler Development, third edition (BSID-III), Gross Motor Function Classification Score (GMFCS) ≥1.

resultsAll twenty-seven neonates enrolled in HEAL were recruited and 3 died before complete recording. The rank-based analysis of covariance models demonstrated lack of difference in NVC between the two groups (Epo versus Placebo) that was consistent with the observed lack of effect on neurodevelopmental outcomes.

conclusionWe demonstrate no difference in neurovascular coupling after Epo administration. These findings are consistent with overall negative trial results. Physiological biomarkers can help elucidate mechanisms of neuroprotective therapies in real time in future trials.

Indexed as

Asphyxia NeonatorumErythropoietinHypoxia-Ischemia, BrainNeurovascular CouplingAsphyxiaBiomarkersHumansInfantInfant, NewbornNeuroprotectionBiomarkersErythropoietinErythropoietinHypoxic ischemic encephalopathyNeuroprotective therapyNeurovascular couplingPhysiological biomarker

Identifiers

PMID37419079
PMCPMC10824020
OpenAlexW4382940764

What OpenQuestion holds

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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.