Evidence map›Paper›PMID 38406838›Full record

ArticlePhysiological genomics2024

The genetic regulation of the gastric transcriptome is associated with metabolic and obesity-related traits and diseases.

Laura L Koebbe, Timo Hess, Ann-Sophie Giel, Jessica Bigge, Jan Gehlen, Vitalia Schueller, Michael Geppert, Franz Ludwig Dumoulin, Joerg Heller, Michael Schepke and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Physiological genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. 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 6 institutions in 1 country.

Laura L KoebbeCenter for Human Genetics, University of Marburg, Marburg, Germany.ORCID 0000-0001-9962-0741
Timo HessCenter for Human Genetics, University of Marburg, Marburg, Germany.
Ann-Sophie GielCenter for Human Genetics, University of Marburg, Marburg, Germany.
Jessica BiggeCenter for Human Genetics, University of Marburg, Marburg, Germany.
Jan GehlenCenter for Human Genetics, University of Marburg, Marburg, Germany.
Vitalia SchuellerCenter for Human Genetics, University of Marburg, Marburg, Germany.
Michael GeppertGastroenterological Centre (Dr. Geppert), Bayreuth, Germany.
Franz Ludwig DumoulinDepartment of Gastroenterology, St. Elisabeth Hospital Bonn, Bonn, Germany.
Joerg HellerMarienhaus Hospital Ahrweiler, Ahrweiler, Germany.
Michael SchepkeDepartment of Gastroenterology, Helios Hospital Siegburg, Siegburg, Germany.
Dominik PlaßmannGastroenterological Centre (Dr. Plassmann), Bonn, Germany.
Michael ViethInstitute for Pathology, Klinikum Bayreuth, University of Erlangen-Nuremberg, Bayreuth, Germany.
Marino VeneritoDepartment of Gastroenterology, Hepatology and Infectious Diseases, Otto-von-Guericke University Hospital, Magdeburg, Germany.
Johannes SchumacherCenter for Human Genetics, University of Marburg, Marburg, Germany.
Carlo MajCenter for Human Genetics, University of Marburg, Marburg, Germany.ORCID 0000-0002-9559-1725
Philipps University of Marburg · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEHelios Hospital Siegburg · DERefonet · DEUniversity Hospital Bonn · DEUniversity Hospital Magdeburg · DE

Funding

German Research Foundation (DFG) SCHU 1596/6-1German Research Foundation (DFG) VE 917-1-1
6 · The paper itself

Abstract

Tissue-specific gene expression and gene regulation lead to a better understanding of tissue-specific physiology and pathophysiology. We analyzed the transcriptome and genetic regulatory profiles of two distinct gastric sites, corpus and antrum, to identify tissue-specific gene expression and its regulation. Gastric corpus and antrum mucosa biopsies were collected during routine gastroscopies from up to 431 healthy individuals. We obtained genotype and transcriptome data and performed transcriptome profiling and expression quantitative trait locus (eQTL) studies. We further used data from genome-wide association studies (GWAS) of various diseases and traits to partition their heritability and to perform transcriptome-wide association studies (TWAS). The transcriptome data from corpus and antral mucosa highlights the heterogeneity of gene expression in the stomach. We identified enriched pathways revealing distinct and common physiological processes in gastric corpus and antrum. Furthermore, we found an enrichment of the single nucleotide polymorphism (SNP)-based heritability of metabolic, obesity-related, and cardiovascular traits and diseases by considering corpus- and antrum-specifically expressed genes. Particularly, we could prioritize gastric-specific candidate genes for multiple metabolic traits, like

Indexed as

Genome-Wide Association StudyTranscriptomeGene Expression RegulationGenetic Predisposition to DiseaseHumansObesityPolymorphism, Single NucleotideStomachexpression quantitative trait locigene expressionmetabolismstomach

Identifiers

PMID38406838
PMCPMC11368570
OpenAlexW4392159322

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.