Evidence map›Paper›PMID 28816579›Full record

ArticleGut microbes2018

Application of the distance-based F test in an mGWAS investigating β diversity of intestinal microbiota identifies variants in SLC9A8 (NHE8) and 3 other loci.

Malte C Rühlemann, Frauke Degenhardt, Louise B Thingholm, Jun Wang, Jurgita Skiecevičienė, Philipp Rausch, Johannes R Hov, Wolfgang Lieb, Tom H Karlsen, Matthias Laudes and 3 more

Abstract readComparative Study
In one paragraph

Article in Gut microbes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

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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

13 authors.

Malte C Rühlemanna Institute of Clinical Molecular Biology , Christian-Albrechts-University of Kiel , Kiel , Germany.
Frauke Degenhardta Institute of Clinical Molecular Biology , Christian-Albrechts-University of Kiel , Kiel , Germany.
Louise B Thingholma Institute of Clinical Molecular Biology , Christian-Albrechts-University of Kiel , Kiel , Germany.
Jun Wangb Evolutionary Genomics , Max Planck Institute for Evolutionary Biology , Plön , Germany.
Jurgita Skiecevičienėa Institute of Clinical Molecular Biology , Christian-Albrechts-University of Kiel , Kiel , Germany.
Philipp Rauschb Evolutionary Genomics , Max Planck Institute for Evolutionary Biology , Plön , Germany.
Johannes R Hovd Norwegian PSC Research Center, Division of Surgery, Inflammatory Medicine and Transplantation , University Hospital Rikshospitalet , Oslo , Norway.
Wolfgang Liebh Institute of Epidemiology , Christian-Albrechts-University of Kiel , Kiel , Germany.
Tom H Karlsend Norwegian PSC Research Center, Division of Surgery, Inflammatory Medicine and Transplantation , University Hospital Rikshospitalet , Oslo , Norway.
Matthias Laudesj Department of Internal Medicine I , University Hospital S.-H. (UKSH, Campus Kiel) , Kiel , Germany.
John F Bainesb Evolutionary Genomics , Max Planck Institute for Evolutionary Biology , Plön , Germany.
Femke-Anouska Heinsena Institute of Clinical Molecular Biology , Christian-Albrechts-University of Kiel , Kiel , Germany.ORCID 0000-0003-3652-6402
Andre Frankea Institute of Clinical Molecular Biology , Christian-Albrechts-University of Kiel , Kiel , Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Factors shaping the human intestinal microbiota range from environmental influences, like smoking and exercise, over dietary patterns and disease to the host's genetic variation. Recently, we could show in a microbiome genome-wide association study (mGWAS) targeting genetic variation influencing the β diversity of gut microbial communities, that approximately 10% of the overall gut microbiome variation can be explained by host genetics. Here, we report on the application of a new method for genotype-β-diversity association testing, the distance-based F (DBF) test. With this we identified 4 loci with genome-wide significant associations, harboring the genes CBEP4, SLC9A8, TNFSF4, and SP140, respectively. Our findings highlight the utility of the high-performance DBF test in β diversity GWAS and emphasize the important role of host genetics and immunity in shaping the human intestinal microbiota.

Indexed as

BiodiversityGastrointestinal MicrobiomeGenome-Wide Association StudyModels, StatisticalAntigens, NuclearBacteriaGenetic LociGenetic VariationHost-Pathogen InteractionsHumansImmunityOX40 LigandReproducibility of ResultsRNA-Binding ProteinsSodium-Hydrogen ExchangersTranscription FactorsAntigens, NuclearCPEB4 protein, humanOX40 LigandRNA-Binding ProteinsSLC9A8 protein, humanSodium-Hydrogen ExchangersSP140 protein, humanTNFSF4 protein, humanTranscription FactorsGWAShuman gut microbiotaIBDimmunityβ diversity

Identifiers

PMID28816579
PMCPMC5939986

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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.