Evidence map›Paper›PMID 38769383›Full record

ArticleScientific reports2024

Angiogenesis-associated pathways play critical roles in neonatal sepsis outcomes.

Mario Fidanza, Julie Hibbert, Erica Acton, Danny Harbeson, Elizna Schoeman, Patrycja Skut, Tabitha Woodman, Adrien Eynaud, Lucy Hartnell, Byron Brook and 13 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

23 authors.

Mario FidanzaTelethon Kids Institute, Perth, WA, Australia.
Julie Hibbert *Westfarmers Center of Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, WA, Australia.
Erica Acton *Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, Canada.
Danny Harbeson *Department of Pediatrics, University of British Columbia, Vancouver, Canada.
Elizna SchoemanTelethon Kids Institute, Perth, WA, Australia.
Patrycja SkutTelethon Kids Institute, Perth, WA, Australia.
Tabitha WoodmanMedical, Molecular and Forensic Sciences, Murdoch University, Perth, WA, Australia.
Adrien EynaudTelethon Kids Institute, Perth, WA, Australia.
Lucy HartnellTelethon Kids Institute, Perth, WA, Australia.
Byron BrookDepartment of Pediatrics, University of British Columbia, Vancouver, Canada.
Bing CaiDepartment of Pediatrics, University of British Columbia, Vancouver, Canada.
Mandy LoDepartment of Pediatrics, University of British Columbia, Vancouver, Canada.
Reza FalsafiDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.
Robert E W HancockDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.
Msandeni Chiume-KayuniDepartment of Pediatrics, Kamuzu Central Hospital, Lilongwe, Malawi.
Norman LufesiDepartment of Curative and Medical Rehabilitation, Ministry of Health, Lilongwe, Malawi.
Constantin R PopescuDepartment of Pediatrics, University of British Columbia, Vancouver, Canada.
Pascal M LavoieDepartment of Pediatrics, University of British Columbia, Vancouver, Canada.
Tobias StrunkTelethon Kids Institute, Perth, WA, Australia.
Andrew J CurrieMedical, Molecular and Forensic Sciences, Murdoch University, Perth, WA, Australia. A.Currie@murdoch.edu.au.
Tobias R KollmannTelethon Kids Institute, Perth, WA, Australia. trkollmann@gmail.com.
Nelly AmenyogbeTelethon Kids Institute, Perth, WA, Australia. n.akuvy@gmail.com.
Amy H LeeDepartment of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, Canada. amy_lee_10@sfu.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neonatal sepsis is a major cause of childhood mortality. Limited diagnostic tools and mechanistic insights have hampered our abilities to develop prophylactic or therapeutic interventions. Biomarkers in human neonatal sepsis have been repeatedly identified as associated with dysregulation of angiopoietin signaling and altered arachidonic acid metabolism. We here provide the mechanistic evidence in support of the relevance for these observations. Angiopoetin-1 (Ang-1), which promotes vascular integrity, was decreased in blood plasma of human and murine septic newborns. In preclinical models, administration of Ang-1 provided prophylactic protection from septic death. Arachidonic acid metabolism appears to be functionally connected to Ang-1 via reactive oxygen species (ROS) with a direct role of nitric oxide (NO). Strengthening this intersection via oral administration of arachidonic acid and/or the NO donor L-arginine provided prophylactic as well as therapeutic protection from septic death while also increasing plasma Ang-1 levels among septic newborns. Our data highlight that targeting angiogenesis-associated pathways with interventions that increase Ang-1 activity directly or indirectly through ROS/eNOS provide promising avenues to prevent and/or treat severe neonatal sepsis.

Indexed as

Angiopoietin-1Neonatal SepsisNitric OxideReactive Oxygen SpeciesAngiogenesisAnimalsAnimals, NewbornArachidonic AcidArginineBiomarkersDisease Models, AnimalFemaleHumansInfant, NewbornMaleMiceAngiopoietin-1ANGPT1 protein, humanArachidonic AcidArginineBiomarkersNitric OxideNitric Oxide Synthase Type IIIReactive Oxygen Species

Identifiers

PMID38769383
PMCPMC11106288

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.