Evidence map›Paper›PMID 28199845›Full record

ArticleCell reports2017

Host Genotype and Gut Microbiome Modulate Insulin Secretion and Diet-Induced Metabolic Phenotypes.

Julia H Kreznar, Mark P Keller, Lindsay L Traeger, Mary E Rabaglia, Kathryn L Schueler, Donald S Stapleton, Wen Zhao, Eugenio I Vivas, Brian S Yandell, Aimee Teo Broman and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed, 1 pooled it
9.4field-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

104 citing papers in PubMed, 1 synthesis or guideline pooled it, 186 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Microorganisms · 2026
    Review
  5. Article
  6. Article
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  17. Article
  18. Impact of Probiotics and Prebiotics on Gut Microbiome and Hormonal Regulation.Gastrointestinal disorders (Basel, Switzerland) · 2024
    Article
  19. Article
  20. Article

44 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

13 authors at 2 institutions in 1 country.

Julia H KreznarDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, USA.
Mark P KellerDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Lindsay L TraegerDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, USA.
Mary E RabagliaDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Kathryn L SchuelerDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Donald S StapletonDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Wen ZhaoDepartment of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, WI 53706, USA.
Eugenio I VivasDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, USA.
Brian S YandellDepartment of Statistics, University of Wisconsin-Madison, Madison, WI 53706, USA; Department of Horticulture, University of Wisconsin-Madison, Madison, WI 53706, USA.
Aimee Teo BromanDepartment of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, WI 53706, USA.
Bruno HagenbuchDepartment of Pharmacology, Toxicology and Therapeutics, University of Kansas, Kansas City, KS 66160, USA.
Alan D AttieDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA. Electronic address: adattie@wisc.edu.
Federico E ReyDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, USA. Electronic address: ferey@wisc.edu.
University of Wisconsin–Madison · USUniversity of Kansas · US

Funding

Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
Research Training for Computation and Informatics in Biology and MedicineT15LM007359 · NLM · UNIVERSITY OF WISCONSIN-MADISON · PI Mark W. Craven, Colin Noel Dewey · 2002 to 2026
$22.6M
THE ROLE OF HUMAN PXR IN ANTI-TUBERCULOSIS DRUG-INDUCED LIVER INJURYP20RR021940 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI KRISHNAMURTHY, PARTHA C · 2006 to 2011
$12.1M
TRAINING IN NUTRITIONT32DK007665 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI GUY E GROBLEWSKI, Chi- Liang Eric Yen · 1993 to 2026
$9.2M
Institutional Clinical and Translational Science AwardKL2TR000428 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$6.2M
The Genetics of Obesity and DiabetesR01DK058037 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI ATTIE, ALAN D · 2001 to 2013
$5.7M
Microbial Pathogenesis &Host Responses Training ProgramT32AI055397 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI KLEIN, BRUCE STEVEN · 2003 to 2024
$5.5M
The Diversity Outbred Diabetes ProjectR01DK101573 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI Alan D Attie · 2014 to 2026
$5.3M
Molecular Characterization of Hepatic Organic Anion Transporting PolypeptidesR01GM077336 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI HAGENBUCH, BRUNO · 2007 to 2019
$3.7M
Collaborative Cross of the Microbiome and Metabolic DiseaseR01DK108259 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI REY, FEDERICO E · 2015 to 2019
$2.1M
The Role of Sorcs1 and Sortilin in Diabetes SusceptibilityR01DK102948 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI ATTIE, ALAN D · 2015 to 2019
$1.7M
NCATS NIH HHS KL2 TR000428NCATS NIH HHS UL1 TR000427NCRR NIH HHS P20 RR021940NIAID NIH HHS T32 AI055397NIDDK NIH HHS R01 DK058037NIDDK NIH HHS R01 DK101573NIDDK NIH HHS R01 DK102948NIDDK NIH HHS R01 DK108259NIDDK NIH HHS T32 DK007665NIGMS NIH HHS R01 GM077336NLM NIH HHS T15 LM007359
6 · The paper itself

Abstract

Genetic variation drives phenotypic diversity and influences the predisposition to metabolic disease. Here, we characterize the metabolic phenotypes of eight genetically distinct inbred mouse strains in response to a high-fat/high-sucrose diet. We found significant variation in diabetes-related phenotypes and gut microbiota composition among the different mouse strains in response to the dietary challenge and identified taxa associated with these traits. Follow-up microbiota transplant experiments showed that altering the composition of the gut microbiota modifies strain-specific susceptibility to diet-induced metabolic disease. Animals harboring microbial communities with enhanced capacity for processing dietary sugars and for generating hydrophobic bile acids showed increased susceptibility to metabolic disease. Notably, differences in glucose-stimulated insulin secretion between different mouse strains were partially recapitulated via gut microbiota transfer. Our results suggest that the gut microbiome contributes to the genetic and phenotypic diversity observed among mouse strains and provide a link between the gut microbiome and insulin secretion.

Indexed as

AnimalsBile Acids and SaltsDiabetes MellitusDiet, High-FatGastrointestinal MicrobiomeGastrointestinal TractGenetic VariationGenotypeInsulinInsulin ResistanceMaleMiceMicrobiotaPhenotypeBile Acids and SaltsInsulingut microbiomeinsulin secretionmetabolic diseasepancreatic islets

Identifiers

PMID28199845
PMCPMC5325228
OpenAlexW2588250592

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.