Evidence map›Paper›PMID 36924810›Full record

ArticleMagnetic resonance imaging2023

Brain BOLD and NIRS response to hyperoxic challenge in sickle cell disease and chronic anemias.

Chau Vu, Adam Bush, Matthew Borzage, Soyoung Choi, Julie Coloigner, Shayan Farzad, Yaqiong Chai, Thomas D Coates, John C Wood

Open access · greenAbstract read
In one paragraph

Article in Magnetic resonance imaging, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Current Progress in the CT- and MRI-Based Detection and Evaluation of Acute Pancreatitis Complications.Medical science monitor : international medical journal of experimental and clinical research · 2025
    Review
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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

9 authors at 3 institutions in 2 countries.

Chau VuDepartment of Biomedical Engineering, University of Southern California, Los Angeles, CA, United States of America.
Adam BushDepartment of Biomedical Engineering, University of Southern California, Los Angeles, CA, United States of America; Department of Biomedical Engineering, University of Texas, Austin, TX, United States of America.
Matthew BorzageDivision of Neonatology, Fetal and Neonatal Institute, Children's Hospital Los Angeles, Los Angeles, CA, United States of America; Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States of America.
Soyoung ChoiNeuroscience Graduate Program, University of Southern California, Los Angeles, CA, United States of America.
Julie ColoignerCIBORG Laboratory, Division of Radiology, Children's Hospital Los Angeles, Los Angeles, CA, United States of America; Univ Rennes, CNRS, Inria, Inserm, IRISA UMR 6074, Empenn ERL U 1228, F-35000 Rennes, France.
Shayan FarzadDepartment of Biomedical Engineering, University of Southern California, Los Angeles, CA, United States of America.
Yaqiong ChaiDepartment of Biomedical Engineering, University of Southern California, Los Angeles, CA, United States of America.
Thomas D CoatesDivision of Hematology-Oncology, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, United States of America; Departments of Pediatrics and Pathology, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States of America.
John C WoodDepartment of Biomedical Engineering, University of Southern California, Los Angeles, CA, United States of America; Division of Cardiology, Departments of Pediatrics and Radiology, Children's Hospital Los Angeles, Los Angeles, CA, United States of America. Electronic address: jwood@chla.usc.edu.
University of Southern California · USChildren's Hospital of Los Angeles · USCentre National de la Recherche Scientifique · FR

Funding

Southern California Clinical and Translational Science InstituteUL1TR001855 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Thomas A Buchanan, Michele D. Kipke · 2016 to 2026
$81.3M
Southern California Clinical and Translational Science InstituteUL1TR000130 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BUCHANAN, THOMAS A · 2012 to 2015
$36.0M
LOS ANGELES BASIN CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR031986 · NCRR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BUCHANAN, THOMAS A · 2010 to 2011
$21.1M
Neuromodulatory Mechanisms and Regional Autonomic Dysregulation in the Development of Pain in Sickle Cell Disease PatientsU01HL117718 · NHLBI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI COATES, THOMAS DUANE, KHOO, MICHAEL C K · 2013 to 2017
$9.6M
Interactive software for semiautomated analysis of structural brain imagesR01NS074980 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LEAHY, RICHARD M, SHATTUCK, DAVID W · 2011 to 2021
$5.0M
Cerebrovascular reserve and white matter disease in patients with anemiaR01HL136484 · NHLBI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI WOOD, JOHN C · 2018 to 2021
$2.5M
Neurological Consequences of AnemiaF31NS106828 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHOI, SOYOUNG · 2018 to 2020
$116k
NCATS NIH HHS UL1 TR000130NCATS NIH HHS UL1 TR001855NCRR NIH HHS UL1 RR031986NHLBI NIH HHS R01 HL136484NHLBI NIH HHS U01 HL117718NINDS NIH HHS F31 NS106828NINDS NIH HHS R01 NS074980
6 · The paper itself

Abstract

purposeCongenital anemias, including sickle cell anemia and thalassemia, are associated with cerebral tissue hypoxia and heightened stroke risks. Recent works in sickle cell disease mouse models have suggested that hyperoxia respiratory challenges can identify regions of the brain having chronic tissue hypoxia. Therefore, this work investigated differences in hyperoxic response and regional cerebral oxygenation between anemic and healthy subjects.

methodsA cohort of 38 sickle cell disease subjects (age 22 ± 8 years, female 39%), 25 non-sickle anemic subjects (age 25 ± 11 years, female 52%), and 31 healthy controls (age 25 ± 10 years, female 68%) were examined. A hyperoxic gas challenge was performed with concurrent acquisition of blood oxygen level-dependent (BOLD) MRI and near-infrared spectroscopy (NIRS). In addition to hyperoxia-induced changes in BOLD and NIRS, global measurements of cerebral blood flow, oxygen delivery, and cerebral metabolic rate of oxygen were obtained and compared between the three groups.

resultsRegional BOLD changes were not able to identify brain regions of flow limitation in chronically anemic patients. Higher blood oxygen content and tissue oxygenation were observed during hyperoxia gas challenge. Both control and anemic groups demonstrated lower blood flow, oxygen delivery, and metabolic rate compared to baseline, but the oxygen metabolism in anemic subjects were abnormally low during hyperoxic exposure.

conclusionThese results indicated that hyperoxic respiratory challenge could not be used to identify chronically ischemic brain. Furthermore, the low hyperoxia-induced metabolic rate suggested potential negative effects of prolonged oxygen therapy and required further studies to evaluate the risk for hyperoxia-induced oxygen toxicity and cerebral dysfunction.

Indexed as

Anemia, Sickle CellHyperoxiaAnimalsBrainCerebrovascular CirculationFemaleHypoxiaMagnetic Resonance ImagingMiceOxygenSpectroscopy, Near-InfraredOxygenBOLD MRIBrainNeurovascular insufficiencyOxygenSickle cell anemia

Identifiers

PMID36924810
PMCPMC10171837
OpenAlexW4324195447

What Socratic 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 Socratic graph.