Evidence map›Paper›PMID 26667607›Full record

ArticleScientific reports2015

Sildenafil Therapy Normalizes the Aberrant Metabolomic Profile in the Comt(-/-) Mouse Model of Preeclampsia/Fetal Growth Restriction.

Joanna L Stanley, Karolina Sulek, Irene J Andersson, Sandra T Davidge, Louise C Kenny, Colin P Sibley, Rupasri Mandal, David S Wishart, David I Broadhurst, Philip N Baker

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Guidelines for assessing maternal cardiovascular physiology during pregnancy and postpartum.American journal of physiology. Heart and circulatory physiology · 2024
    Guideline
  2. Article
  3. Regulation of maternal-fetal metabolic communication.Cellular and molecular life sciences : CMLS · 2021
    Review
  4. Catechol-O-methyltransferase and Pregnancy Outcome: an Appraisal in Rat.Reproductive sciences (Thousand Oaks, Calif.) · 2021
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. 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

10 authors at 5 institutions in 4 countries.

Joanna L StanleyLiggins Institute, University of Auckland, New Zealand.
Karolina SulekLiggins Institute, University of Auckland, New Zealand.
Irene J AnderssonDepartment of Medicine, University of Alberta, Edmonton, Canada.
Sandra T DavidgeWomen and Children's Health Research Institute, University of Alberta, Edmonton, Canada.
Louise C KennyAnu Research Centre, University College Cork, Ireland.
Colin P SibleyMaternal &Fetal Health Research Centre, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, UK.
Rupasri MandalThe Metabolomics Innovation Centre (TMIC), University of Alberta, Edmonton, Canada.
David S WishartThe Metabolomics Innovation Centre (TMIC), University of Alberta, Edmonton, Canada.
David I BroadhurstDepartment of Medicine, University of Alberta, Edmonton, Canada.
Philip N BakerLiggins Institute, University of Auckland, New Zealand.
University of Alberta · CAUniversity of Auckland · NZThe Metabolomics Innovation Centre · CAUniversity College Cork · IEUniversity of Manchester · GB

Funding

Medical Research Council
6 · The paper itself

Abstract

Preeclampsia (PE) and fetal growth restriction (FGR) are serious complications of pregnancy, associated with greatly increased risk of maternal and perinatal morbidity and mortality. These complications are difficult to diagnose and no curative treatments are available. We hypothesized that the metabolomic signature of two models of disease, catechol-O-methyl transferase (COMT(-/-)) and endothelial nitric oxide synthase (Nos3(-/-)) knockout mice, would be significantly different from control C57BL/6J mice. Further, we hypothesised that any differences in COMT(-/-) mice would be resolved following treatment with Sildenafil, a treatment which rescues fetal growth. Targeted, quantitative comparisons of serum metabolic profiles of pregnant Nos3(-/-), COMT(-/-) and C57BL/6J mice were made using a kit from BIOCRATES. Significant differences in 4 metabolites were observed between Nos3(-/-) and C57BL/6J mice (p < 0.05) and in 18 metabolites between C57BL/6J and COMT(-/-) mice (p < 0.05). Following treatment with Sildenafil, only 5 of the 18 previously identified differences in metabolites (p < 0.05) remained in COMT(-/-) mice. Metabolomic profiling of mouse models is possible, producing signatures that are clearly different from control animals. A potential new treatment, Sildenafil, is able to normalize the aberrant metabolomic profile in COMT(-/-) mice; as this treatment moves into clinical trials, this information may assist in assessing possible mechanisms of action.

Indexed as

AnimalsCatechol O-MethyltransferaseDisease Models, AnimalFemaleFetal Growth RetardationMetabolomeMetabolomicsMiceMice, KnockoutPre-EclampsiaPregnancySildenafil CitrateCatechol O-MethyltransferaseSildenafil Citrate

Identifiers

PMID26667607
PMCPMC4678899
OpenAlexW2207920818

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.