Evidence map›Paper›PMID 26378058›Full record

ArticleEndocrine connections2015

Born from pre-eclamptic pregnancies predisposes infants to altered cortisol metabolism in the first postnatal year.

Fiona Broughton Pipkin, Hiten D Mistry, Chandrima Roy, Bernhard Dick, Jason Waugh, Rebecca Chikhi, Lesia O Kurlak, Markus G Mohaupt

Open access · goldAbstract read
In one paragraph

Article in Endocrine connections, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 86% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 3 institutions in 2 countries.

Fiona Broughton PipkinDepartment of Obstetrics and GynaecologySchool of Medicine, University of Nottingham, Nottingham, NG5 1PB, UKDepartment of NephrologyHypertension and Clinical Pharmacology, Clinical Research, University of Bern, 3010 Berne, SwitzerlandLeicester Royal InfirmaryLeicester, LE1 5WW, UK.
Hiten D MistryDepartment of Obstetrics and GynaecologySchool of Medicine, University of Nottingham, Nottingham, NG5 1PB, UKDepartment of NephrologyHypertension and Clinical Pharmacology, Clinical Research, University of Bern, 3010 Berne, SwitzerlandLeicester Royal InfirmaryLeicester, LE1 5WW, UK.
Chandrima RoyDepartment of Obstetrics and GynaecologySchool of Medicine, University of Nottingham, Nottingham, NG5 1PB, UKDepartment of NephrologyHypertension and Clinical Pharmacology, Clinical Research, University of Bern, 3010 Berne, SwitzerlandLeicester Royal InfirmaryLeicester, LE1 5WW, UK.
Bernhard DickDepartment of Obstetrics and GynaecologySchool of Medicine, University of Nottingham, Nottingham, NG5 1PB, UKDepartment of NephrologyHypertension and Clinical Pharmacology, Clinical Research, University of Bern, 3010 Berne, SwitzerlandLeicester Royal InfirmaryLeicester, LE1 5WW, UK.
Jason WaughDepartment of Obstetrics and GynaecologySchool of Medicine, University of Nottingham, Nottingham, NG5 1PB, UKDepartment of NephrologyHypertension and Clinical Pharmacology, Clinical Research, University of Bern, 3010 Berne, SwitzerlandLeicester Royal InfirmaryLeicester, LE1 5WW, UK.
Rebecca ChikhiDepartment of Obstetrics and GynaecologySchool of Medicine, University of Nottingham, Nottingham, NG5 1PB, UKDepartment of NephrologyHypertension and Clinical Pharmacology, Clinical Research, University of Bern, 3010 Berne, SwitzerlandLeicester Royal InfirmaryLeicester, LE1 5WW, UK.
Lesia O KurlakDepartment of Obstetrics and GynaecologySchool of Medicine, University of Nottingham, Nottingham, NG5 1PB, UKDepartment of NephrologyHypertension and Clinical Pharmacology, Clinical Research, University of Bern, 3010 Berne, SwitzerlandLeicester Royal InfirmaryLeicester, LE1 5WW, UK.
Markus G MohauptDepartment of Obstetrics and GynaecologySchool of Medicine, University of Nottingham, Nottingham, NG5 1PB, UKDepartment of NephrologyHypertension and Clinical Pharmacology, Clinical Research, University of Bern, 3010 Berne, SwitzerlandLeicester Royal InfirmaryLeicester, LE1 5WW, UK markus.mohaupt@insel.ch.
University of Bern · CHLeicester Royal Infirmary · GBUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pre-eclampsia leads to disturbed fetal organ development, including metabolic syndrome, attributed to altered pituitary-adrenal feedback loop. We measured cortisol metabolites in infants born from pre-eclamptic and normotensive women and hypothesised that glucocorticoid exposure would be exaggerated in the former. Twenty-four hour urine was collected from infants at months 3 and 12. Cortisol metabolites and apparent enzyme activities were analysed by gas chromatography-mass spectrometry. From 3 to 12 months, excretion of THS, THF and pregnandiol had risen in both groups; THF also rose in the pre-eclamptic group. No difference was observed with respect to timing of the visit or to hypertensive status for THE or total F metabolites (P>0.05). All apparent enzymes activities, except 17α-hydroxylase, were lower in infants at 12 compared to 3 months in the normotensive group. In the pre-eclamptic group, only 11β-HSD activities were lower at 12 months.17α-hydroxylase and 11β-HSD activities of tetrahydro metabolites were higher in the pre-eclamptic group at 3 months (P<0.05). 11β-hydroxylase activity increased in the pre-eclamptic group at 12 months. Cortisol excretion, determined by increased 11β-hydroxylase, compensates for high 11β-HSD-dependent cortisol degradation at 3 months and at 12 months counterbalances the reduced cortisol substrate availability in infants born from pre-eclamptic mothers.

Indexed as

infantspre-eclampsiasteroid hormonesurine

Identifiers

PMID26378058
PMCPMC4621850
OpenAlexW2341715791

What OpenQuestion holds

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LicenceCC BY
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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.