Evidence map›Paper›PMID 27666579›Full record

ArticleGenome biology2016

Heritable components of the human fecal microbiome are associated with visceral fat.

Michelle Beaumont, Julia K Goodrich, Matthew A Jackson, Idil Yet, Emily R Davenport, Sara Vieira-Silva, Justine Debelius, Tess Pallister, Massimo Mangino, Jeroen Raes and 5 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed, 1 pooled it
14.3field-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

119 citing papers in PubMed, 1 synthesis or guideline pooled it, 242 citations in OpenAlex.

  1. Pooled it
  2. Testosterone administration partially modulates gut microbiota responses to severe energy deficit.American journal of physiology. Endocrinology and metabolism · 2026
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  6. FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
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59 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

15 authors at 7 institutions in 4 countries.

Michelle BeaumontDepartment of Twin Research & Genetic Epidemiology, King's College London, St Thomas' Hospital, 3rd Floor, South Wing, Block D, London, SE1 7EH, UK.
Julia K GoodrichDepartment of Microbiology, Cornell University, Ithaca, NY, 14853, USA.
Matthew A JacksonDepartment of Twin Research & Genetic Epidemiology, King's College London, St Thomas' Hospital, 3rd Floor, South Wing, Block D, London, SE1 7EH, UK.
Idil YetDepartment of Twin Research & Genetic Epidemiology, King's College London, St Thomas' Hospital, 3rd Floor, South Wing, Block D, London, SE1 7EH, UK.
Emily R DavenportDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY, 14853, USA.
Sara Vieira-SilvaDepartment of Microbiology and Immunology, KU Leuven - University of Leuven, Leuven, Belgium.
Justine DebeliusDepartment of Chemistry and Biochemistry, University of Colorado, Boulder, CO, 80309, USA.
Tess PallisterDepartment of Twin Research & Genetic Epidemiology, King's College London, St Thomas' Hospital, 3rd Floor, South Wing, Block D, London, SE1 7EH, UK.
Massimo ManginoDepartment of Twin Research & Genetic Epidemiology, King's College London, St Thomas' Hospital, 3rd Floor, South Wing, Block D, London, SE1 7EH, UK.
Jeroen RaesDepartment of Microbiology and Immunology, KU Leuven - University of Leuven, Leuven, Belgium.
Rob KnightDepartment of Chemistry and Biochemistry, University of Colorado, Boulder, CO, 80309, USA.
Andrew G ClarkDepartment of Microbiology, Cornell University, Ithaca, NY, 14853, USA.
Ruth E LeyDepartment of Microbiology, Cornell University, Ithaca, NY, 14853, USA.
Tim D SpectorDepartment of Twin Research & Genetic Epidemiology, King's College London, St Thomas' Hospital, 3rd Floor, South Wing, Block D, London, SE1 7EH, UK. tim.spector@kcl.ac.uk.
Jordana T BellDepartment of Twin Research & Genetic Epidemiology, King's College London, St Thomas' Hospital, 3rd Floor, South Wing, Block D, London, SE1 7EH, UK. jordana.bell@kcl.ac.uk.
King's College London · GBCornell University · USSt Thomas' Hospital · GBKU Leuven · BEUniversity of California, San Diego · USUniversity of Colorado Boulder · USVIB-UGent Center for Plant Systems Biology · BE

Funding

Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
Genetic Transmission of Components of the Human Gut MicrobiomeR01DK093595 · NIDDK · CORNELL UNIVERSITY · PI CLARK, ANDREW G, LEY, RUTH EMILY · 2011 to 2020
$3.5M
Modeling Human Gut Microbiome Community Structure in Healthy and Diseased StatesF32DK109595 · NIDDK · CORNELL UNIVERSITY · PI DAVENPORT, EMILY · 2016 to 2018
$173k
European Research Council 250157Medical Research Council MR/N030125/1NIDDK NIH HHS R01 DK093595Wellcome Trust
6 · The paper itself

Abstract

backgroundVariation in the human fecal microbiota has previously been associated with body mass index (BMI). Although obesity is a global health burden, the accumulation of abdominal visceral fat is the specific cardio-metabolic disease risk factor. Here, we explore links between the fecal microbiota and abdominal adiposity using body composition as measured by dual-energy X-ray absorptiometry in a large sample of twins from the TwinsUK cohort, comparing fecal 16S rRNA diversity profiles with six adiposity measures.

resultsWe profile six adiposity measures in 3666 twins and estimate their heritability, finding novel evidence for strong genetic effects underlying visceral fat and android/gynoid ratio. We confirm the association of lower diversity of the fecal microbiome with obesity and adiposity measures, and then compare the association between fecal microbial composition and the adiposity phenotypes in a discovery subsample of twins. We identify associations between the relative abundances of fecal microbial operational taxonomic units (OTUs) and abdominal adiposity measures. Most of these results involve visceral fat associations, with the strongest associations between visceral fat and Oscillospira members. Using BMI as a surrogate phenotype, we pursue replication in independent samples from three population-based cohorts including American Gut, Flemish Gut Flora Project and the extended TwinsUK cohort. Meta-analyses across the replication samples indicate that 8 OTUs replicate at a stringent threshold across all cohorts, while 49 OTUs achieve nominal significance in at least one replication sample. Heritability analysis of the adiposity-associated microbial OTUs prompted us to assess host genetic-microbe interactions at obesity-associated human candidate loci. We observe significant associations of adiposity-OTU abundances with host genetic variants in the FHIT, TDRG1 and ELAVL4 genes, suggesting a potential role for host genes to mediate the link between the fecal microbiome and obesity.

conclusionsOur results provide novel insights into the role of the fecal microbiota in cardio-metabolic disease with clear potential for prevention and novel therapies.

Indexed as

Fecal microbiomeGenetic associationHeritabilityObesityTwinsVisceral fat

Identifiers

PMID27666579
PMCPMC5036307
OpenAlexW2521421819

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.