Evidence map›Paper›PMID 31826255›Full record

ArticleThe American journal of clinical nutrition2020

The role of the gut microbiome in the association between habitual anthocyanin intake and visceral abdominal fat in population-level analysis.

Amy Jennings, Manja Koch, Majken K Jensen, Corinna Bang, Jan Kassubek, Hans-Peter Müller, Ute Nöthlings, Andre Franke, Wolfgang Lieb, Aedín Cassidy

Abstract read
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Article in The American journal of clinical nutrition, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Wild blueberries and cardiometabolic health: a current review of the evidence.Critical reviews in food science and nutrition · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Anthocyanins in Colorectal Cancer Prevention Review.Antioxidants (Basel, Switzerland) · 2021
    Review
  14. Review
  15. A Guide to Diet-Microbiome Study Design.Frontiers in nutrition · 2020
    Review
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

10 authors.

Amy JenningsDepartment of Nutrition and Preventive Medicine, Norwich Medical School, University of East Anglia, Norwich, United Kingdom.
Manja KochDepartment of Nutrition, Harvard TH Chan School of Public Health, Boston, MA, USA.
Majken K JensenDepartment of Nutrition, Harvard TH Chan School of Public Health, Boston, MA, USA.
Corinna BangInstitute of Clinical Molecular Biology, Kiel University, Kiel, Germany.
Jan KassubekDepartment of Neurology, University of Ulm, Ulm, Germany.
Hans-Peter MüllerDepartment of Neurology, University of Ulm, Ulm, Germany.
Ute NöthlingsDepartment of Nutrition and Food Sciences, University of Bonn, Bonn, Germany.
Andre FrankeInstitute of Clinical Molecular Biology, Kiel University, Kiel, Germany.
Wolfgang LiebInstitute of Epidemiology, Kiel University, Kiel, Germany.
Aedín CassidyInstitute for Global Food Security, Queen's University Belfast, Belfast, United Kingdom.

Funding

Biotechnology and Biological Sciences Research Council BB/J004545/1
6 · The paper itself

Abstract

backgroundFlavonoid intake modifies the composition of the gut microbiome, which contributes to the metabolism of flavonoids. Few studies have examined the contribution of the gut microbiome to the health benefits associated with flavonoid intake.

objectivesWe aimed to examine associations between habitual intakes of flavonoid subclasses and MRI-determined visceral (VAT) and subcutaneous (SAT) adipose tissue. Uniquely, we also identified associations between the aforementioned measurements and gut microbiome composition sequenced from 16S ribosomal RNA genes.

methodsWe undertook cross-sectional analyses of 618 men and women (n = 368 male), aged 25-83 y, from the PopGen cohort.

resultsHigher intake of anthocyanins was associated with lower amounts of VAT [tertile (T)3-T1:  -0.49 dm3; β: -8.9%; 95% CI: -16.2%, -1.1%; P = 0.03] and VAT:SAT ratio (T3-T1: -0.04; β: -7.1%; 95% CI: -13.5%, -0.3%; P = 0.03). Higher intakes of anthocyanin-rich foods were also inversely associated with VAT [quantile (Q)4-Q1: -0.39 dm3; β: -9.9%; 95% CI: -17.4%, -1.6%; P = 0.02] and VAT:SAT ratio (Q4-Q1: -0.04; β: -6.5%; 95% CI: -13.3%, -0.9%; P = 0.03). Participants with the highest intakes of anthocyanin-rich foods also had higher microbial diversity (Q4-Q1: β: 0.18; 95% CI: 0.06, 0.31; P < 0.01), higher abundances of Clostridiales (Q4-Q1: β: 449; 95% CI: 96.3, 801; P = 0.04) and Ruminococcaceae (Q4-Q1: β: 313; 95% CI: 33.6, 591; P = 0.04), and lower abundance of Clostridium XIVa (Q4-Q1: β: -41.1; 95% CI: -72.4, -9.8; P = 0.04). Participants with the highest microbial diversity, abundances of Clostridiales and Ruminococcaceae, and lower abundance of Clostridium XIVa had lower amounts of VAT. Up to 18.5% of the association between intake of anthocyanin-rich foods and VAT could be explained by the gut microbiome.

conclusionsThese novel data suggest that higher microbial diversity and abundance of specific taxa in the Clostridiales order may contribute to the association between higher intake of anthocyanins and lower abdominal adipose tissue.

Indexed as

Gastrointestinal MicrobiomeAdultAgedAged, 80 and overAnthocyaninsBacteriaFemaleHumansIntra-Abdominal FatMaleMiddle AgedSubcutaneous Fat, AbdominalAnthocyaninsabdominal adipose tissueanthocyaninsflavonoidsgut microbiotamicrobial diversitysubcutaneous fatvisceral fat

Identifiers

PMID31826255
PMCPMC6997102

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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.