Evidence map›Paper›PMID 38362586›Full record

ArticleFrontiers in endocrinology2023

Asymmetric growth-limiting development of the female conceptus.

Consuelo Amor S Estrella, Kathryn L Gatford, Ruidong Xiang, Ali Javadmanesh, Mani Ghanipoor-Samami, Greg S Nattrass, Entesar Shuaib, Milton M McAllister, Ian Beckman, Dana A Thomsen and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2023. 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
7.8field-weighted citation impact, top 3% 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, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

15 authors at 4 institutions in 1 country.

Consuelo Amor S EstrellaRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
Kathryn L GatfordRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
Ruidong XiangRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
Ali JavadmaneshRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
Mani Ghanipoor-SamamiRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
Greg S NattrassSouth Australian Research and Development Institute, Livestock Systems, Roseworthy, SA, Australia.
Entesar ShuaibRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
Milton M McAllisterSchool of Animal and Veterinary Sciences, The University of Adelaide, Roseworthy, SA, Australia.
Ian BeckmanSchool of Animal and Veterinary Sciences, The University of Adelaide, Roseworthy, SA, Australia.
Dana A ThomsenRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
Vicki L CliftonRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
Julie A OwensRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
Claire T RobertsRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
Stefan HiendlederRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
Karen L KindRobinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
University of Adelaide · AUDeakin University · AUFlinders University · AUSouth Australian Research and Development Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Sex differences in prenatal growth may contribute to sex-dependent programming effects on postnatal phenotype. Methods: We integrated for the first time phenotypic, histomorphological, clinico-chemical, endocrine and gene expression analyses in a single species, the bovine conceptus at mid-gestation. Results: We demonstrate that by mid-gestation, before the onset of accelerated growth, the female conceptus displays asymmetric lower growth compared to males. Female fetuses were smaller with lower ponderal index and organ weights than males. However, their brain:body weight, brain:liver weight and heart:body weight ratios were higher than in males, indicating brain and heart 'sparing'. The female placenta weighed less and had lower volumes of trophoblast and fetal connective tissue than the male placenta. Female umbilical cord vessel diameters were smaller, and female-specific relationships of body weight and brain:liver weight ratios with cord vessel diameters indicated that the umbilico-placental vascular system creates a growth-limiting environment where blood flow is redistributed to protect brain and heart growth. Clinico-chemical indicators of liver perfusion support this female-specific growth-limiting phenotype, while lower insulin-like growth factor 2 (IGF2) gene expression in brain and heart, and lower circulating IGF2, implicate female-specific modulation of key endocrine mediators by nutrient supply. Conclusion: This mode of female development may increase resilience to environmental perturbations

Indexed as

FetusPlacentaAnimalsBody WeightCattleFemaleLiverMalePregnancyTrophoblastsasymmetric growthclinico-chemical screenconceptushistomorphologyIGF systemsex differencesuncomplicated pregnancy

Identifiers

PMID38362586
PMCPMC10867182
OpenAlexW4391444319

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.