Evidence map›Paper›PMID 25879645›Full record

ArticleReproductive biology and endocrinology : RB&E2015

Offspring subcutaneous adipose markers are sensitive to the timing of maternal gestational weight gain.

Linda Giblin, Christian Darimont, Patricia Leone, Louise B McNamara, Florence Blancher, Donagh Berry, Eurídice Castañeda-Gutiérrez, Peadar G Lawlor

Open access · goldAbstract read
In one paragraph

Article in Reproductive biology and endocrinology : RB&E, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.3field-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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Secondary bile acids are associated with body lipid accumulation in obese pigs.Animal nutrition (Zhongguo xu mu shou yi xue hui) · 2024
    Article
  2. 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

8 authors at 2 institutions in 2 countries.

Linda GiblinTeagasc Food Research Centre, Moorepark, Fermoy, Co.Cork, Ireland. Linda.Giblin@teagasc.ie.
Christian DarimontNestlé Research Centre, Nutrition & Health Research Department, Vers-Chez-les-Blanc, Lausanne, Switzerland. christian.darimont@rdls.nestle.com.
Patricia LeoneNestlé Research Centre, Nutrition & Health Research Department, Vers-Chez-les-Blanc, Lausanne, Switzerland. patricia.leone@rdls.nestle.com.
Louise B McNamaraTeagasc Food Research Centre, Moorepark, Fermoy, Co.Cork, Ireland. louisemcnamara@gmail.com.
Florence BlancherNestlé Research Centre, Nutrition & Health Research Department, Vers-Chez-les-Blanc, Lausanne, Switzerland. Florence.Blancher@rdls.nestle.com.
Donagh BerryAnimal and Grassland Research and Innovation Centre, Teagasc, Moorepark, Fermoy, Co. Cork, Ireland. Donagh.Berry@teagasc.ie.
Eurídice Castañeda-GutiérrezNestlé Research Centre, Nutrition & Health Research Department, Vers-Chez-les-Blanc, Lausanne, Switzerland. Euridice.CastanedaGutierrez@rdls.nestle.com.
Peadar G LawlorAnimal and Grassland Research and Innovation Centre, Teagasc, Moorepark, Fermoy, Co. Cork, Ireland. Peadar.Lawlor@teagasc.ie.
Nestlé (Switzerland) · CHTeagasc - The Irish Agriculture and Food Development Authority · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExcessive maternal weight gain during pregnancy impacts on offspring health. This study focused on the timing of maternal gestational weight gain, using a porcine model with mothers of normal pre-pregnancy weight.

methodsTrial design ensured the trajectory of maternal gestational weight gain differed across treatments in early, mid and late gestation. Diet composition did not differ. On day 25 gestation, sows were assigned to one of five treatments: Control sows received a standard gestation diet of 2.3 kg/day (30 MJ DE/day) from early to late gestation (day 25-110 gestation). E sows received 4.6 kg food/day in early gestation (day 25-50 gestation). M sows doubled their food intake in mid gestation (day 50-80 gestation). EM sows doubled their food intake during both early and mid gestation (day 25-80 gestation). L sows consumed 3.5 kg food/day in late gestation (day 80-110 gestation). Offspring body weight and food intake levels were measured from birth to adolescence. Markers of lipid metabolism, hypertrophy and inflammation were investigated in subcutaneous adipose tissue of adolescent offspring.

resultsThe trajectory of gestational weight gain differed across treatments. However total gestational weight gain did not differ except for EM sows who were the heaviest and fattest mothers at parturition. Offspring birth weight did not differ across treatments. Subcutaneous adipose tissue from EM offspring differed significantly from controls, with elevated mRNA levels of lipogenic (CD36, ACACB and LPL), nutrient transporters (FABP4 and GLUT4), lipolysis (HSL and ATGL), adipocyte size (MEST) and inflammation (PAI-1) indicators. The subcutaneous adipose depot from L offspring exhibited elevated levels of CD36, ACACB, LPL, GLUT4 and FABP4 mRNA transcripts compared to control offspring.

conclusionsIncreasing gestational weight gain in early gestation had the greatest impact on offspring postnatal growth rate. Increasing maternal food allowance in late gestation appeared to shift the offspring adipocyte focus towards accumulation of fat. Mothers who gained the most weight during gestation (EM mothers) gave birth to offspring whose subcutaneous adipose tissue, at adolescence, appeared hyperactive compared to controls. This study concluded that mothers, who gained more than the recommended weight gain in mid and late gestation, put their offspring adipose tissue at risk of dysfunction.

Indexed as

Weight GainAdipose TissueAnimalsBiomarkersBody Fat DistributionEatingFemaleGestational AgeHumansPregnancyPrenatal Exposure Delayed EffectsSwineTime FactorsBiomarkers

Identifiers

PMID25879645
PMCPMC4363193
OpenAlexW2127461626

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.