Evidence map›Paper›PMID 35106835›Full record

ArticleActa paediatrica (Oslo, Norway : 1992)2022

Proteomic profiles in cerebrospinal fluid predicted death and disability in term infants with perinatal asphyxia: A pilot study.

Kristin Leifsdottir, Eric P Thelin, Philipp Lassarén, Veronica Siljehav, Peter Nilsson, Staffan Eksborg, Eric Herlenius

Open access · hybridAbstract read
In one paragraph

Article in Acta paediatrica (Oslo, Norway : 1992), 2022. 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
1.5field-weighted citation impact, top 18% 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, 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 3 institutions in 1 country.

Kristin LeifsdottirDepartment of Women´s and Children´s Health, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0003-0491-7302
Eric P ThelinDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-2338-4364
Philipp LassarénDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0003-0833-1093
Veronica SiljehavDepartment of Women´s and Children´s Health, Karolinska Institutet, Stockholm, Sweden.
Peter NilssonDepartment of Protein Science, KTH Royal Institute of Technology, SciLifeLab, Stockholm, Sweden.ORCID 0000-0002-4657-8532
Staffan EksborgDepartment of Women´s and Children´s Health, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-7326-9471
Eric HerleniusDepartment of Women´s and Children´s Health, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-6859-0620
Karolinska University Hospital · SEKarolinska Institutet · SEScience for Life Laboratory · SE

Funding

Axel Tielmans, Freemasons Childern's House and the Swedish National Heart and Lung 20180505Region Stockholm 20190400Swedish Brain Foundation FO2019-0006Swedish Brain Foundation FO2019-0087Swedish Research Council 2019-01157
6 · The paper itself

Abstract

aimPerinatal asphyxia, resulting in hypoxic-ischaemic encephalopathy (HIE), has been associated with high mortality rates and severe lifelong neurodevelopmental disabilities. Our aim was to study the association between the proteomic profile in cerebrospinal fluid (CSF) and the degree of HIE and long-term outcomes.

methodsWe prospectively enrolled 18-term born infants with HIE and 10-term born controls between 2000 and 2004 from the Karolinska University Hospital. An antibody suspension bead array and FlexMap3D analysis was used to characterise 178 unique brain-derived and inflammation associated proteins in their CSF.

resultsIncreased CSF concentrations of several brain-specific proteins were observed in the proteome of HIE patients compared with the controls. An upregulation of neuroinflammatory pathways was also noted and this was confirmed by pathway analysis. Principal component analysis revealed a gradient from favourable to unfavourable HIE grades and outcomes. The proteins that provided strong predictors were structural proteins, including myelin basic protein and alpha-II spectrin. The functional proteins included energy-related proteins like neuron-specific enolase and synaptic regulatory proteins. Increased CSF levels of 51 proteins correlated with adverse outcomes in infants with HIE.

conclusionBrain-specific proteins and neuroinflammatory mediators in CSF may predict HIE degrees and outcomes after perinatal asphyxia.

Indexed as

Asphyxia NeonatorumHypoxia-Ischemia, BrainAsphyxiaFemaleHumansInfantInfant, NewbornPilot ProjectsPregnancyProteomicsbiomarkerscerebrospinal fluidhypoxic-ischaemic encephalopathyperinatal asphyxiaprotein profile

Identifiers

PMID35106835
PMCPMC9305740
OpenAlexW4210559661

What OpenQuestion holds

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LicenceCC BY-NC
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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.