Evidence map›Paper›PMID 30819197›Full record

ArticleJournal of translational medicine2019

Increased expression and phosphorylation of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase isoforms in urinary exosomes in pre-eclampsia.

R Ellis, M Katerelos, S W Choy, N Cook, M Lee, K Paizis, G Pell, S Walker, D A Power, P F Mount

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Observational
  4. Article
  5. Review
  6. Extracellular Vesicles as Biomarkers of Pregnancy Complications.International journal of molecular sciences · 2024
    Review
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  8. Article
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  10. Article
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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

10 authors at 4 institutions in 1 country.

R EllisFaculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Australia.
M KaterelosDepartment of Nephrology, Austin Health, Studley Road, Heidelberg, Melbourne, VIC, 3084, Australia.
S W ChoyDepartment of Nephrology, Austin Health, Studley Road, Heidelberg, Melbourne, VIC, 3084, Australia.
N CookDepartment of Nephrology, Austin Health, Studley Road, Heidelberg, Melbourne, VIC, 3084, Australia.
M LeeFaculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Australia.
K PaizisDepartment of Nephrology, Austin Health, Studley Road, Heidelberg, Melbourne, VIC, 3084, Australia.
G PellMercy Hospital for Women, Heidelberg, Australia.
S WalkerMercy Hospital for Women, Heidelberg, Australia.
D A PowerFaculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Australia.
P F MountFaculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Australia. peter.mount@austin.org.au.ORCID 0000-0001-7637-3661
The University of Melbourne · AUAustin Health · AUMercy Hospital for Women · AUInstitute for Breathing and Sleep · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlycolysis is altered in various kidney diseases, but little is known about glycolysis in pre-eclampsia, a multi-system disorder with major pathological effects on the kidney. Urinary exosomes provide a non-invasive alternative for studying changes in kidney metabolism. This study aims to characterise the expression and phosphorylation of isozymes of the key glycolytic regulatory protein, 6-phosphofructokinase-2-kinase/fructose-2,6-bisphosphatase (PFK-2/FBPase-2), in urinary exosomes of subjects with pre-eclampsia (PE), compared to normotensive non-pregnant (NC) and normotensive pregnant (NP) controls.

methodsA cross-sectional study of NC (n = 19), NP (n = 23) and PE (n = 29) subjects was performed. Exosomes were isolated from urine samples by differential ultracentrifugation, and then analyzed by Western blot and densitometry for expression of PFK-2/FBPase-2 isozymes (PFKFB2, PFKFB3 and PFKFB4) and phosphorylation of PFKFB2 at residues Ser483 and Ser466 and PFKFB3 at Ser461.

resultsPFKFB2 expression was increased 4.7-fold in PE compared to NP (p < 0.001). PFKFB2 phosphorylation at Ser483 was increased 2.6-fold in PE compared to NP (p = 0.002). Expression of phosphorylated PFKFB2/PFKFB3 at Ser466/Ser461 was increased in PE, being present in 77.4% (95% CI 59.9-88.9%) of PE and 8.3% (95% CI 1.2-27.0%) of NP samples (p < 0.001). PFKFB3 was more commonly expressed in PE, detected in 90.3% (95% CI 74.3-97.4%) of PE and 8.3% (95% CI 1.2-27.0%) of NP samples (p < 0.001). PFKFB4 had a 7.2-fold increase in expression in PE compared to NP (p < 0.001). No significant differences between NP and NC groups were observed.

conclusionRegulatory proteins that increase glycolysis are increased in the urinary exosomes of subjects with pre-eclampsia, suggesting that renal glycolysis may be increased in this condition.

Indexed as

AdultExosomesFemaleGlycolysisHumansIsoenzymesPhosphofructokinase-2PhosphorylationPhosphoserinePre-EclampsiaPregnancyYoung AdultIsoenzymesPFKFB3 protein, humanPFKFB4 protein, humanPhosphofructokinase-2Phosphoserine6-Bisphosphatase6-Phosphofructo-2-kinase/fructose-2GlycolysisPhosphorylationPre-eclampsiaUrinary exosomes

Identifiers

PMID30819197
PMCPMC6394033
OpenAlexW2939041766

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.