Evidence map›Paper›PMID 29795201›Full record

ArticlePediatric research2018

Characterization and origin of heme precursors in amniotic fluid: lessons from normal and pathological pregnancies.

Hana Manceau, Vincent Puy, Caroline M Schmitt, Sophie Gil, Thibaud Lefebvre, Bichr Allaf, Jonathan Rosenblatt, Laurent Gouya, Hervé Puy, Francoise Muller and 1 more

Open access · bronzeAbstract read
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In one paragraph

Article in Pediatric research, 2018. 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
0.1field-weighted citation impact, top 53% 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, 1 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

11 authors at 8 institutions in 1 country.

Hana Manceau *Biochimie Clinique, Hôpital Beaujon, APHP, HUPNVS, Clichy, France.
Vincent Puy *Reproductive Medicine and Medical Cytogenetics Department, Regional University Hospital and School of Medicine, Amiens, France.
Caroline M SchmittUMRs 1149, Centre de Recherche sur l'Inflammation, Institut National de la Santé et de la Recherche Médicale, F-75018, Paris, France.
Sophie GilUMRs1139, UFR des Sciences Pharmaceutiques, Université Paris Descartes, Paris, France.
Thibaud LefebvreUMRs 1149, Centre de Recherche sur l'Inflammation, Institut National de la Santé et de la Recherche Médicale, F-75018, Paris, France.
Bichr AllafBiochimie-Hormonologie, Hôpital Robert Debré, APHP, Paris, France.
Jonathan RosenblattGynécologie-Obstétrique, Hôpital Robert Debré, APHP, Paris, France.
Laurent GouyaUMRs 1149, Centre de Recherche sur l'Inflammation, Institut National de la Santé et de la Recherche Médicale, F-75018, Paris, France.
Hervé Puy *UMRs 1149, Centre de Recherche sur l'Inflammation, Institut National de la Santé et de la Recherche Médicale, F-75018, Paris, France.
Francoise Muller *Biochimie-Hormonologie, Hôpital Robert Debré, APHP, Paris, France.
Katell Peoc'h *Biochimie Clinique, Hôpital Beaujon, APHP, HUPNVS, Clichy, France. katell.peoch@aphp.fr.
Assistance Publique – Hôpitaux de Paris · FRHôpital Louis-Mourier · FRCentre de Recherche sur l'Inflammation · FRCentre Hospitalier Universitaire Amiens-Picardie · FRDélégation Paris 5 · FRHôpital Beaujon · FRInserm · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeme is the prosthetic group of numerous proteins involved in vital processes such as oxygen transport, oxidative stress, and energetic mitochondrial metabolism. Free heme also plays a significant role at early stages of development and in cell differentiation processes. The metabolism of heme by the fetal placenta unit is not well-established in humans.

methodsIn a retrospective study, we measured heme precursors in the amniotic fluid (AF) of 51 healthy women, and 10 AF samples from pregnancies with either upper or lower intestinal atresia or ileus were also analyzed.

resultsWe showed that the porphyrin precursors aminolevulinic acid, porphobilinogen, and protoporphyrin IX are present at the limit of detection in the AF. Total porphyrin levels decreased progressively from week 13 to week 33 (p < 0.01). Interestingly, uroporphyrin, initially detected as traces, increased with maturation, in contrast to coproporphyrin. Uro- and coproporphyrins were type I immature isomers (>90%), suggesting a lack of maturity in the fetal compartment of the heme pathway. Finally, the differential analysis of AF from normal and pathological pregnancies demonstrated the predominant hepatic origin of fetal porphyrins excreted in the AF.

conclusionThis study gives the first insight into heme metabolism in the AF during normal and pathological pregnancies.

Indexed as

AdultAmniocentesisAmniotic FluidCell DifferentiationCoproporphyrinsFemaleHemeHumansIleusIntestinal AtresiaKaryotypingMaternal AgeMitochondriaOxidative StressOxygenPlacentaCoproporphyrinsHemeOxygenprotoporphyrin IXProtoporphyrinsUroporphyrins

Identifiers

PMID29795201
OpenAlexW2804657953

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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.