Evidence map›Paper›PMID 19864158›Full record

ReviewTrends in endocrinology and metabolism: TEM2010

Epigenetic mechanisms in the development of type 2 diabetes.

Sara E Pinney, Rebecca A Simmons

Abstract readReview
In one paragraph

Review in Trends in endocrinology and metabolism: TEM, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
21.3field-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

80 citing papers in PubMed, 199 citations in OpenAlex.

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20 more citing papers are in PubMed but not listed here.

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.

Sara E PinneyDepartment of Pediatrics, The Children's Hospital Philadelphia, Philadelphia, PA 19104, USA.
Rebecca A Simmons
Children's Hospital of Philadelphia · US

Funding

MECHANISMS BY WHICH IUGR LEADS TO DIABETESR01DK055704 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI SIMMONS, REBECCA A · 2000 to 2014
$3.6M
Mechanisms by which GDM Leads to Diabetes in OffspringR01AG020898 · NIA · UNIVERSITY OF PENNSYLVANIA · PI SIMMONS, REBECCA A · 2001 to 2005
$1.6M
NIA NIH HHS R01 AG020898NICHD NIH HHS K12HD0432545NIDDK NIH HHS DK55704NIDDK NIH HHS L40 DK079770NIDDK NIH HHS R01 DK055704
6 · The paper itself

Abstract

Type 2 diabetes (T2D) is a disorder of complex genetics influenced by interactions between susceptible genetic loci and environmental perturbations. Intrauterine growth retardation is one such environmental perturbation linked to the development of T2D in adulthood. An abnormal metabolic intrauterine milieu affects fetal development by permanently modifying expression of key genes regulating beta-cell development (Pdx1) and glucose transport (Glut4) in muscle. Epigenetic regulation of gene expression is one mechanism by which genetic susceptibility and environmental insults can lead to T2D. Therefore, therapeutic agents targeting epigenetic gene regulation can ultimately be used to treat T2D; however, there is much to be learned about genome-wide epigenetic programming of health and disease before these therapies can be used in patient care.

Indexed as

Epigenesis, GeneticChromatin Assembly and DisassemblyDiabetes Mellitus, Type 2Fetal Growth RetardationGene Expression RegulationGlucose Transporter Type 4HistonesHomeodomain ProteinsHumansOxidative StressTrans-ActivatorsGlucose Transporter Type 4HistonesHomeodomain Proteinspancreatic and duodenal homeobox 1 proteinSLC2A4 protein, humanTrans-Activators

Identifiers

PMID19864158
PMCPMC2848901
OpenAlexW1977200537

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.