Evidence map›Paper›PMID 29899523›Full record

ArticleInternational journal of obesity (2005)2018

Relation of placental alkaline phosphatase expression in human term placenta with maternal and offspring fat mass.

Birgit Hirschmugl, Sarah Crozier, Nina Matthews, Eva Kitzinger, Ingeborg Klymiuk, Hazel M Inskip, Nicholas C Harvey, Cyrus Cooper, Colin P Sibley, Jocelyn Glazier and 4 more

Open access · greenAbstract read
In one paragraph

Article in International journal of obesity (2005), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.6field-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

7 citing papers in PubMed, 14 citations in OpenAlex.

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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

14 authors at 5 institutions in 2 countries.

Birgit HirschmuglDepartment of Obstetrics and Gynaecology, Medical University of Graz, Graz, Austria.
Sarah CrozierMRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, UK.
Nina MatthewsMRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, UK.
Eva KitzingerDepartment of Obstetrics and Gynaecology, Medical University of Graz, Graz, Austria.
Ingeborg KlymiukCore Facility Molecular Biology, Centre for Medical Research, Medical University of Graz, Graz, Austria.
Hazel M InskipMRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, UK.
Nicholas C HarveyMRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, UK.
Cyrus CooperMRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, UK.
Colin P SibleyMaternal and Fetal Health Research Centre, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9WL, UK.ORCID http://orcid.org/0000-0002-2713-0492
Jocelyn GlazierMaternal and Fetal Health Research Centre, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9WL, UK.
Christian WadsackDepartment of Obstetrics and Gynaecology, Medical University of Graz, Graz, Austria.
Keith M GodfreyMRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, UK.
Gernot DesoyeDepartment of Obstetrics and Gynaecology, Medical University of Graz, Graz, Austria.
Rohan M LewisFaculty of Medicine, University of Southampton, Southampton, UK. Rohan.Lewis@soton.ac.uk.ORCID http://orcid.org/0000-0003-4044-9104
Medical University of Graz · ATMRC Lifecourse Epidemiology Unit · GBManchester Academic Health Science Centre · GBUniversity Hospital Southampton NHS Foundation Trust · GBUniversity of Southampton · GB

Funding

British Heart Foundation RG/15/17/31749Department of Health 10/33/04Medical Research Council G0400491Medical Research Council MC_U147574222Medical Research Council MC_U147574226Medical Research Council MC_U147585819Medical Research Council MC_U147585827Medical Research Council MC_UP_A620_1014Medical Research Council MC_UP_A620_1017Medical Research Council MC_UU_12011/1Medical Research Council MC_UU_12011/4Medical Research Council MR/J000094/1Versus Arthritis 17702Versus Arthritis 21231
6 · The paper itself

Abstract

introductionAlkaline phosphatase is implicated in intestinal lipid transport and in the development of obesity. Placental alkaline phosphatase is localised to the microvillous plasma membrane of the placental syncytiotrophoblast at the maternal-fetal interface, but its role is unclear. We investigated the relations of placental alkaline phosphatase activity and mRNA expression with maternal body composition and offspring fat mass in humans.

methodsTerm human placentas from the UK Birthright cohort (n = 52) and the Southampton Women's Survey (SWS) (n = 95) were studied. In the Birthright cohort, alkaline phosphatase activity was measured in placental microvillous plasma membrane vesicles. In the SWS, alkaline phosphatase mRNA was measured using Nanostring. Alkaline phosphatase gene expression was compared to other lipid-related genes.

resultsIn Birthright samples placental microvillous plasma membrane alkaline phosphatase activity was positively associated with maternal triceps skinfold thickness and BMI (β = 0.04 (95% CI: 0.01-0.06) and β = 0.02 (0.00-0.03) µmol/mg protein/min per SD, P = 0.002 and P = 0.05, respectively) after adjusting for potential confounders. In SWS samples placental alkaline phosphatase mRNA expression in term placenta was positively associated with maternal triceps skinfold (β = 0.24 (0.04, 0.44) SD/SD, P = 0.02), had no association with neonatal %fat mass (β = 0.01 (-0.20 to 0.21) SD/SD, P = 0.93) and was negatively correlated with %fat mass at ages 4 (β = -0.28 (-0.52 to -0.04) SD/SD, P = 0.02), 6-7 (β = -0.25 (-0.49 to -0.02) SD/SD, P = 0.03) years. When compared with placental expression of other genes, alkaline phosphatase expression was positively related to genes including the lysophosphatidylcholine transporter MFSD2A (major facilitator superfamily domain containing 2A, P < 0.001) and negatively related to genes including the fatty acid transport proteins 2 and 3 (P = 0.001, P < 0.001).

conclusionsOur findings suggest relationships between placental alkaline phosphatase and both maternal and childhood adiposity. The inverse relationship between placental alkaline phosphatase gene expression and childhood %fat mass suggests that placental alkaline phosphatase may help to protect the foetus from the adverse effects of maternal obesity.

Indexed as

AdultAlkaline PhosphataseBiological TransportBody CompositionChild DevelopmentCohort StudiesFemaleGPI-Linked ProteinsHumansInfant, NewbornIsoenzymesObesityPregnancyPrenatal Exposure Delayed EffectsSymportersTerm BirthAlkaline Phosphatasealkaline phosphatase, placentalGPI-Linked ProteinsIsoenzymesMFSD2A protein, humanSymportersTumor Suppressor Proteins

Identifiers

PMID29899523
PMCPMC6173293
OpenAlexW2807809259

What OpenQuestion holds

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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.