Evidence map›Paper›PMID 36541220›Full record

ArticlePhysiological reports2022

Neonatal hypoxic ischemic encephalopathy increases acute kidney injury urinary biomarkers in a rat model.

Angela M Groves, Carl J Johnston, Gisela G Beutner, Jane E Dahlstrom, Mark Koina, Michael A O'Reilly, George Porter, Patrick D Brophy, Alison L Kent

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
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.

Angela M GrovesDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, New York, Rochester, USA.ORCID 0000-0003-1810-5532
Carl J JohnstonDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, New York, Rochester, USA.
Gisela G BeutnerDivision of Cardiology, University of Rochester School of Medicine and Dentistry, New York, Rochester, USA.
Jane E DahlstromDepartment of Anatomical Pathology, ACT Pathology, Canberra Health Services, Canberra, Australia.
Mark KoinaDepartment of Anatomical Pathology, ACT Pathology, Canberra Health Services, Canberra, Australia.
Michael A O'ReillyDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, New York, Rochester, USA.
George PorterDivision of Cardiology, University of Rochester School of Medicine and Dentistry, New York, Rochester, USA.
Patrick D BrophyDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, New York, Rochester, USA.
Alison L KentDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, New York, Rochester, USA.
University of Rochester · USAustralian National University · AUUniversity of Rochester Medical Center · US

Funding

VISUAL INDICES OF NEUROTOXICITYP30ES001247 · NIEHS · UNIVERSITY OF ROCHESTER · PI Martha Susiarjo · 1985 to 2026
$42.8M
Effect of Neonatal Hyperoxia on Alveolar Development and InfectionR01HL091968 · NHLBI · UNIVERSITY OF ROCHESTER · PI O'REILLY, MICHAEL A · 2009 to 2021
$5.4M
Cyclophilin D Regulates Neonatal Cardiac Bioenergetics and FunctionR01HL144776 · NHLBI · UNIVERSITY OF ROCHESTER · PI PORTER, GEORGE A · 2019 to 2022
$2.0M
NHLBI NIH HHS R01 HL091968NHLBI NIH HHS R01 HL144776NIEHS NIH HHS P30 ES001247
6 · The paper itself

Abstract

Hypoxic ischemic encephalopathy (HIE) is associated with acute kidney injury (AKI) in neonates with birth asphyxia. This study aimed to utilize urinary biomarkers to characterize AKI in an established neonatal rat model of HIE. Day 7 Sprague-Dawley rat pups underwent HIE using the Rice-Vannucci model (unilateral carotid ligation followed by 120 mins of 8% oxygen). Controls included no surgery and sham surgery. Weights and urine for biomarkers (NGAL, osteopontin, KIM-1, albumin) were collected the day prior, daily for 3 days post-intervention, and at sacrifice day 14. Kidneys and brains were processed for histology. HIE pups displayed histological evidence of kidney injury including damage to the proximal tubules, consistent with resolving acute tubular necrosis, and had significantly elevated urinary levels of NGAL and albumin compared to sham or controls 1-day post-insult that elevated for 3 days. KIM-1 significantly increased for 2 days post-HIE. HIE did not significantly alter osteopontin levels. Seven days post-start of experiment, controls were 81.2% above starting weight compared to 52.1% in HIE pups. NGAL and albumin levels inversely correlated with body weight following HIE injury. The AKI produced by the Rice-Vannucci HIE model is detectable by urinary biomarkers, which can be used for future studies of treatments to reduce kidney injury.

Indexed as

Acute Kidney InjuryHypoxia-Ischemia, BrainAnimalsBiomarkersLipocalin-2OsteopontinRatsRats, Sprague-DawleyBiomarkersLipocalin-2OsteopontinAKIHIEurinary biomarkers

Identifiers

PMID36541220
PMCPMC9768655
OpenAlexW4312194619

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.