Evidence map›Paper›PMID 28925408›Full record

ArticleInternational journal of obesity (2005)2018

Liver volume and hepatic adiposity in childhood: relations to body growth and visceral fat.

R Malpique, J Bassols, A López-Bermejo, M Diaz, F Villarroya, J Pavia, A Congo, F de Zegher, L Ibáñez

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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 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 14% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
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  3. Article
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  5. 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

9 authors at 7 institutions in 2 countries.

R MalpiqueEndocrinology, Pediatric Research Institute Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
J BassolsDepartment of Pediatrics, Hospital Dr Josep Trueta and Girona Institute for Biomedical Research, Girona, Spain.
A López-BermejoDepartment of Pediatrics, Hospital Dr Josep Trueta and Girona Institute for Biomedical Research, Girona, Spain.
M DiazEndocrinology, Pediatric Research Institute Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
F VillarroyaBiochemical and Molecular Biology Department, Biomedicine Institute, University of Barcelona, Barcelona, Spain.
J PaviaCETIR Medical Center, Barcelona, Spain.
A CongoCETIR Medical Center, Barcelona, Spain.
F de ZegherDepartment of Development and Regeneration, University of Leuven, Leuven, Belgium.
L IbáñezEndocrinology, Pediatric Research Institute Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
Institut d'Investigació Biomèdica de Girona · ESUniversitat de Barcelona · ESBiomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine · ESCenter of Regenerative Medicine in Barcelona · ESHospital Sant Joan de Déu Barcelona · ESInstitute for Research in Biomedicine · ESKU Leuven · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveThe sequence of prenatal growth restraint and postnatal catch-up growth may lead to hepato-visceral adiposity, insulin resistance and low-grade inflammation before the onset of puberty. In prepubertal children born appropriate for gestational age (AGA) or small for gestational age (SGA), we assessed potential relationships between the aforementioned sequence and liver volume. SUBJECTS/

methodsThe study population consisted of 86 children (41 AGA and 45 SGA with catch-up growth; age (mean±s.e.m.), 8.5±0.1 years), recruited into two prospective longitudinal studies. Anthropometry, endocrine-metabolic variables and inflammatory and hepatic markers were assessed, along with liver volume, hepatic adiposity and abdominal fat partitioning (by magnetic resonance imaging).

resultsAGA and SGA children differed in hepato-visceral adiposity, but had similar liver volumes. Boys had larger livers than girls, and higher sex hormone binding globulin and inflammation markers. Liver volume correlated with height Z-score, body mass index Z-score, HOMA-IR (homeostasis model assessment-insulin resistance) and with subcutaneous and visceral fat, but not with birth weight Z-score or with hepatic adiposity. Height, visceral fat, gender and HOMA-IR were major determinants of liver volume, together explaining 61% of its variance.

conclusionsThe trajectory from prenatal restraint, via postnatal catch-up, to hepato-visceral adiposity and insulin resistance does not appear to be detectably influenced by prepubertal alterations of liver volume. Further follow-up will disclose the potential role of liver volume in the pubertal segment of this trajectory, and whether the augmented fat content and visceral adiposity in SGA subjects is followed by the development of metabolic syndrome and hepatic dysfunction in adulthood.

Indexed as

ChildFatty LiverFemaleGrowth ChartsHumansInfant, NewbornInfant, Small for Gestational AgeIntra-Abdominal FatLiverLongitudinal StudiesMaleMultivariate AnalysisOverweightPediatric ObesityProspective StudiesRisk Factors

Identifiers

PMID28925408
OpenAlexW2747689738

What OpenQuestion holds

Textmetadata
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.