Evidence map›Paper›PMID 28675387›Full record

ArticleTranslational psychiatry2017

Serotonin transporter gene promoter methylation status correlates with in vivo prefrontal 5-HTT availability and reward function in human obesity.

M Drabe, M Rullmann, J Luthardt, Y Boettcher, R Regenthal, T Ploetz, G A Becker, M Patt, C Schinke, F T Bergh and 7 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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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

17 authors at 2 institutions in 2 countries.

M DrabeIntegrated Research and Treatment Centre AdiposityDiseases, University of Leipzig, Leipzig, Germany.
M RullmannIntegrated Research and Treatment Centre AdiposityDiseases, University of Leipzig, Leipzig, Germany.
J LuthardtDepartment of Nuclear Medicine, University of Leipzig, Leipzig, Germany.
Y BoettcherIntegrated Research and Treatment Centre AdiposityDiseases, University of Leipzig, Leipzig, Germany.
R RegenthalDivision of Clinical Pharmacology, Rudolf-Boehm-Institute for Pharmacology and Toxicology, University of Leipzig, Leipzig, Germany.
T PloetzDivision of Clinical Pharmacology, Rudolf-Boehm-Institute for Pharmacology and Toxicology, University of Leipzig, Leipzig, Germany.
G A BeckerDepartment of Nuclear Medicine, University of Leipzig, Leipzig, Germany.
M PattDepartment of Nuclear Medicine, University of Leipzig, Leipzig, Germany.
C SchinkeIntegrated Research and Treatment Centre AdiposityDiseases, University of Leipzig, Leipzig, Germany.
F T BerghDepartment of Neurology, University of Leipzig, Leipzig, Germany.
F ZientekIntegrated Research and Treatment Centre AdiposityDiseases, University of Leipzig, Leipzig, Germany.
A HilbertIntegrated Research and Treatment Centre AdiposityDiseases, University of Leipzig, Leipzig, Germany.
A BreschDepartment of Nuclear Medicine, University of Leipzig, Leipzig, Germany.
W FenskeIntegrated Research and Treatment Centre AdiposityDiseases, University of Leipzig, Leipzig, Germany.
M K HankirIntegrated Research and Treatment Centre AdiposityDiseases, University of Leipzig, Leipzig, Germany.
O SabriIntegrated Research and Treatment Centre AdiposityDiseases, University of Leipzig, Leipzig, Germany.
S HesseIntegrated Research and Treatment Centre AdiposityDiseases, University of Leipzig, Leipzig, Germany.
Leipzig University · DEIFB Adiposity Diseases · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A polymorphism in the promoter region of the human serotonin transporter (5-HTT)-coding SLC6A4 gene (5-HTTLPR) has been implicated in moderating susceptibility to stress-related psychopathology and to possess regulatory functions on human in vivo 5-HTT availability. However, data on a direct relation between 5-HTTLPR and in vivo 5-HTT availability have been inconsistent. Additional factors such as epigenetic modifications of 5-HTTLPR might contribute to this association. This is of particular interest in the context of obesity, as an association with 5-HTTLPR hypermethylation has previously been reported. Here, we tested the hypothesis that methylation rates of 14 cytosine-phosphate-guanine (CpG) 5-HTTLPR loci, in vivo central 5-HTT availability as measured with [

Indexed as

DNA MethylationRewardAdultEpigenesis, GeneticFemaleHumansMaleObesityPolymorphism, GeneticPrefrontal CortexPromoter Regions, GeneticSerotonin Plasma Membrane Transport ProteinsSerotonin Plasma Membrane Transport ProteinsSLC6A4 protein, human

Identifiers

PMID28675387
PMCPMC5538116
OpenAlexW2730013809

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.