Evidence map›Paper›PMID 34080727›Full record

ArticleAnnals of neurology2021

Longitudinal CSF Iron Pathway Proteins in Posthemorrhagic Hydrocephalus: Associations with Ventricle Size and Neurodevelopmental Outcomes.

Jennifer M Strahle, Kelly B Mahaney, Diego M Morales, Chandana Buddhala, Chevis N Shannon, John C Wellons, Abhaya V Kulkarni, Hailey Jensen, Ron W Reeder, Richard Holubkov and 9 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Annals of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
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  8. Paediatric hydrocephalus.Nature reviews. Disease primers · 2024
    Review
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  17. Observational
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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

19 authors at 10 institutions in 2 countries.

Jennifer M StrahleDepartment of Neurosurgery, Washington University St. Louis, St. Louis, MO, USA.
Kelly B MahaneyDepartment of Neurosurgery, Stanford University, Palo Alto, CA, USA.
Diego M MoralesDepartment of Neurosurgery, Washington University St. Louis, St. Louis, MO, USA.ORCID 0000-0001-6672-9046
Chandana BuddhalaDepartment of Neurosurgery, Washington University St. Louis, St. Louis, MO, USA.
Chevis N ShannonDepartment of Neurosurgery, Vanderbilt University Medical Center, Nashville, TN, USA.
John C WellonsDepartment of Neurosurgery, Vanderbilt University Medical Center, Nashville, TN, USA.
Abhaya V KulkarniDepartment of Neurosurgery, University of Toronto, Toronto, Ontario, Canada.
Hailey JensenData Coordinating Center, University of Utah, Salt Lake City, UT, USA.
Ron W ReederData Coordinating Center, University of Utah, Salt Lake City, UT, USA.
Richard HolubkovData Coordinating Center, University of Utah, Salt Lake City, UT, USA.
Jay K Riva-CambrinDepartment of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
William E WhiteheadDepartment of Neurosurgery, Baylor College of Medicine, Houston, TX, USA.
Curtis J RozzelleDepartment of Neurosurgery, University of Alabama - Birmingham, Birmingham, AL, USA.
Mandeep TamberDepartment of Surgery, University of British Columbia, Vancouver, British Columbia, Canada.
Ian F PollackDepartment of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Robert P NaftelDepartment of Neurosurgery, Vanderbilt University Medical Center, Nashville, TN, USA.
John R W KestleDepartment of Neurosurgery, University of Utah, Salt Lake City, UT, USA.
David D LimbrickDepartment of Neurosurgery, Washington University St. Louis, St. Louis, MO, USA.
Hydrocephalus Clinical Research Network
University of Utah · USWashington University in St. Louis · USVanderbilt University Medical Center · USBaylor College of Medicine · USStanford University · USUniversity of Alabama at Birmingham · USUniversity of British Columbia · CAUniversity of Calgary · CAUniversity of Pittsburgh Medical Center · USUniversity of Toronto · CA

Funding

Endoscopic versus Shunt Treatment of Hydrocephalus in InfantsU01NS107486 · NINDS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Richard Holubkov, John Kestle · 2019 to 2026
$9.6M
Ependymal Dysfunction in Neonatal Post-Hemorrhagic HydrocephalusR01NS110793 · NINDS · WASHINGTON UNIVERSITY · PI STRAHLE, JENNIFER · 2019 to 2023
$2.5M
Hydrocephalus Clinical Research Network: a consortium for pediatric hydrocephalusRC1NS068943 · NINDS · UNIVERSITY OF UTAH · PI KESTLE, JOHN · 2009 to 2010
$995k
CSF LEVELS OF L1CAM AND AMYLOID PRECURSOR PROTEIN IN POST-HEMORRHAGIC HYDROCEPHALK23NS075151 · NINDS · WASHINGTON UNIVERSITY · PI LIMBRICK, DAVID DELMAR · 2012 to 2016
$843k
Doris Duke Charitable FoundationHydrocephalus AssociationNIH HHS 1RC1NS068943NINDS NIH HHS K23 NS075151NINDS NIH HHS NS075151NINDS NIH HHS NS110793NINDS NIH HHS R01 NS110793NINDS NIH HHS RC1 NS068943NINDS NIH HHS U01 NS107486Patient-Centered Outcomes Research Institute CER-1403-13857
6 · The paper itself

Abstract

objectiveIron has been implicated in the pathogenesis of brain injury and hydrocephalus after preterm germinal matrix hemorrhage-intraventricular hemorrhage, however, it is unknown how external or endogenous intraventricular clearance of iron pathway proteins affect the outcome in this group.

methodsThis prospective multicenter cohort included patients with posthemorrhagic hydrocephalus (PHH) who underwent (1) temporary and permanent cerebrospinal fluid (CSF) diversion and (2) Bayley Scales of Infant Development-III testing around 2 years of age. CSF proteins in the iron handling pathway were analyzed longitudinally and compared to ventricle size and neurodevelopmental outcomes.

resultsThirty-seven patients met inclusion criteria with a median estimated gestational age at birth of 25 weeks; 65% were boys. Ventricular CSF levels of hemoglobin, iron, total bilirubin, and ferritin decreased between temporary and permanent CSF diversion with no change in CSF levels of ceruloplasmin, transferrin, haptoglobin, and hepcidin. There was an increase in CSF hemopexin during this interval. Larger ventricle size at permanent CSF diversion was associated with elevated CSF ferritin (p = 0.015) and decreased CSF hemopexin (p = 0.007). CSF levels of proteins at temporary CSF diversion were not associated with outcome, however, higher CSF transferrin at permanent CSF diversion was associated with improved cognitive outcome (p = 0.015). Importantly, longitudinal change in CSF iron pathway proteins, ferritin (decrease), and transferrin (increase) were associated with improved cognitive (p = 0.04) and motor (p = 0.03) scores and improved cognitive (p = 0.04), language (p = 0.035), and motor (p = 0.008) scores, respectively.

interpretationLongitudinal changes in CSF transferrin (increase) and ferritin (decrease) are associated with improved neurodevelopmental outcomes in neonatal PHH, with implications for understanding the pathogenesis of poor outcomes in PHH. ANN NEUROL 2021;90:217-226.

Indexed as

Cerebral VentriclesCerebral HemorrhageCerebrospinal Fluid ProteinsCerebrospinal Fluid ShuntsChild DevelopmentChild, PreschoolCohort StudiesFemaleFerritinsHumansHydrocephalusInfantInfant, NewbornInfant, PrematureIronLongitudinal StudiesCerebrospinal Fluid ProteinsFerritinsIronTransferrin

Identifiers

PMID34080727
PMCPMC8702098
OpenAlexW3164321658

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Registered trials

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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.