Evidence map›Paper›PMID 38433703›Full record

ArticleDiabetes, obesity & metabolism2024

Accelerated onset of diabetes in non-obese diabetic mice fed a refined high-fat diet.

Heidi M Batdorf, Luz de Luna Lawes, Gabrielle A Cassagne, Molly S Fontenot, Innocence C Harvey, Jeremy T Richardson, David H Burk, Samuel D Dupuy, Michael D Karlstad, J Michael Salbaum and 5 more

Open access · greenAbstract read
In one paragraph

Article in Diabetes, obesity & metabolism, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

15 authors at 2 institutions in 1 country.

Heidi M BatdorfPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Luz de Luna LawesPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Gabrielle A CassagnePennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Molly S FontenotPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Innocence C HarveyPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Jeremy T RichardsonPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
David H BurkPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Samuel D DupuyDepartment of Surgery, University of Tennessee Health Science Center, Graduate School of Medicine, Knoxville, Tennessee, USA.
Michael D KarlstadDepartment of Surgery, University of Tennessee Health Science Center, Graduate School of Medicine, Knoxville, Tennessee, USA.
J Michael SalbaumPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Jaroslaw StaszkiewiczPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Robbie BeylPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Sujoy GhoshPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Susan J BurkePennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
J Jason CollierPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.ORCID 0000-0003-2817-4152
Pennington Biomedical Research Center · USUniversity of Tennessee Health Science Center · US

Funding

Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI ROBERT A KESTERSON · 2005 to 2026
$26.5M
The role of maternal obesity-driven inflammation and adverse pregnancy outcomes in a mouse model of preeclampsiaP20GM135002 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Jacqueline M Stephens · 2020 to 2026
$18.4M
SGK1 is a regulator of islet beta cell mass and secretory functionR01DK123183 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI COLLIER, JAMES JASON · 2020 to 2024
$1.8M
Sable Systems Promethion for Mouse Metabolic AnalysisS10OD023703 · OD · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MORRISON, CHRISTOPHER D · 2017 to 2017
$626k
NIDDK NIH HHS P30 DK072476NIDDK NIH HHS R01 DK123183NIGMS NIH HHS P20 GM135002NIH HHS S10 OD023703
6 · The paper itself

Abstract

aimType 1 diabetes results from autoimmune events influenced by environmental variables, including changes in diet. This study investigated how feeding refined versus unrefined (aka 'chow') diets affects the onset and progression of hyperglycaemia in non-obese diabetic (NOD) mice.

methodsFemale NOD mice were fed either unrefined diets or matched refined low- and high-fat diets. The onset of hyperglycaemia, glucose tolerance, food intake, energy expenditure, circulating insulin, liver gene expression and microbiome changes were measured for each dietary group.

resultsNOD mice consuming unrefined (chow) diets developed hyperglycaemia at similar frequencies. By contrast, mice consuming the defined high-fat diet had an accelerated onset of hyperglycaemia compared to the matched low-fat diet. There was no change in food intake, energy expenditure, or physical activity within each respective dietary group. Microbiome changes were driven by diet type, with chow diets clustering similarly, while refined low- and high-fat bacterial diversity also grouped closely. In the defined dietary cohort, liver gene expression changes in high-fat-fed mice were consistent with a greater frequency of hyperglycaemia and impaired glucose tolerance.

conclusionGlucose intolerance is associated with an enhanced frequency of hyperglycaemia in female NOD mice fed a defined high-fat diet. Using an appropriate matched control diet is an essential experimental variable when studying changes in microbiome composition and diet as a modifier of disease risk.

Indexed as

Diabetes Mellitus, Type 1Diet, High-FatHyperglycemiaMice, Inbred NODAnimalsBlood GlucoseDiet, Fat-RestrictedEnergy MetabolismFemaleGlucose IntoleranceInsulinLiverMiceBlood GlucoseInsulinautoimmunitydiabetesdietmicrobiomenon‐obese diabetic (NOD) mouse modelobesity

Identifiers

PMID38433703
PMCPMC11078605
OpenAlexW4392374380

What OpenQuestion 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 OpenQuestion graph.