Evidence map›Paper›PMID 19663040›Full record

ReviewCurrent opinion in pediatrics2009

The developmental origins of adult disease.

Lisa A Joss-Moore, Robert H Lane

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in pediatrics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
13.8field-weighted citation impact, top 1% 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

31 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
  2. Article
  3. Sex, hormones, and lung health.Physiological reviews · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Observational
  10. BaByVFSSImPDysphagia · 2020
    Article
  11. Article
  12. Tyrosine phosphorylation of Kv1.5 is upregulated in intrauterine growth retardation rats with exaggerated pulmonary hypertension.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Association of low-protein supplemented diets with fetal growth in pregnant women with CKD.Clinical journal of the American Society of Nephrology : CJASN · 2014
    Article
  17. Review
  18. Article
  19. Article
  20. Predicting later-life outcomes of early-life exposures.Environmental health perspectives · 2012
    Review
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

2 authors at 1 institution in 1 country.

Lisa A Joss-MooreDivision of Neonatology, Department of Pediatrics,University of Utah, 295 Chipeta Way, 2N131 Salt Lake City, UT 84108, USA.
Robert H Lane
University of Utah · US

Funding

Maternal Diet Modifies the Fetal Primate Epigenome and Circadian Gene ExpressionR01DK080558 · NIDDK · UNIVERSITY OF UTAH · PI LANE, ROBERT H · 2007 to 2010
$987k
NIDDK NIH HHS R01 DK080558
6 · The paper itself

Abstract

purpose of reviewIntrauterine growth restriction (IUGR) is associated with an increased propensity to develop adult-onset disease and is described by the developmental origins of adult disease hypothesis. Sequelae of fetal growth restriction include metabolic disease as well as nonmetabolic disorders. Although it has become clear that the morbidities associated with IUGR are complex and result from disruptions to multiple pathways and multiple organs, the mechanisms driving the long-term effects are only just beginning to be understood. RECENT

findingsIUGR affects most organ systems by either interrupting developmental processes such as apoptosis or producing lasting changes to levels of key regulatory factors. Both of these are associated with an often persistent change in gene expression. Epigenetic modulation of transcription is a mechanism that is at least partially responsible for this. IUGR is accompanied by changes in the quantity and activity of enzymes responsible for making modifications to chromatin as well as global and gene-specific modifications of chromatin. SUMMARY: The subtle adjustments needed to ensure developmental plasticity in IUGR are provided by epigenetic modulation of critical genes. Translating the messages of the epigenetic profile and identifying the players that mediate the effects remains one of the major challenges in the field. An understanding of the mechanisms driving the epigenetic changes will facilitate identification of dietary and pharmaceutical approaches that can be applied in the postnatal period.

Indexed as

Fetal Growth RetardationAdultAnimalsApoptosisChronic DiseaseDisease ProgressionEpigenesis, GeneticFetal DevelopmentGene Expression Regulation, DevelopmentalHumansMetabolic DiseasesObesityYoung Adult

Identifiers

PMID19663040
PMCPMC2726974
OpenAlexW2038137111

What OpenQuestion holds

Textmetadata
LicenceTDM
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.