Evidence map›Paper›PMID 29901267›Full record

ArticleObesity (Silver Spring, Md.)2018

Liquid Sucrose Consumption Promotes Obesity and Impairs Glucose Tolerance Without Altering Circulating Insulin Levels.

Susan J Burke, Heidi M Batdorf, Thomas M Martin, David H Burk, Robert C Noland, Christopher R Cooley, Michael D Karlstad, William D Johnson, J Jason Collier

Open access · bronzeAbstract read
In one paragraph

Article in Obesity (Silver Spring, Md.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Susan J BurkePennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Heidi M BatdorfPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Thomas M MartinPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
David H BurkPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Robert C NolandPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Christopher R CooleyDepartment of Surgery, Graduate School of Medicine, University of Tennessee Health Science Center, Knoxville, Tennessee, USA.
Michael D KarlstadDepartment of Surgery, Graduate School of Medicine, University of Tennessee Health Science Center, Knoxville, Tennessee, USA.
William D JohnsonPennington 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

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2005 to 2026
$26.5M
THE ROLE OF PROTEIN MALNUTRITION ON CIRCADIAN PHYSIOLOGY OF C57BL/6J MOUSE DAMSP20RR021945 · NCRR · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2006 to 2011
$9.5M
Mentoring Obesity and Diabetes Research in LouisianaP20GM103528 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2012 to 2015
$8.8M
Transgenics CoreP30GM118430 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2016 to 2020
$5.8M
Defining the role of skeletal muscle peroxisomes in glucose homeostasisR01DK103860 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI NOLAND, ROBERT CHARLES · 2015 to 2019
$1.7M
Sable Systems Promethion for Mouse Metabolic AnalysisS10OD023703 · OD · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MORRISON, CHRISTOPHER D · 2017 to 2017
$626k
NCRR NIH HHS P20 RR021945NIDDK NIH HHS P30 DK072476NIDDK NIH HHS R01 DK103860NIGMS NIH HHS P20 GM103528NIGMS NIH HHS P30 GM118430NIGMS NIH HHS U54 GM104940NIH HHS S10 OD023703
6 · The paper itself

Abstract

objectiveMultiple factors contribute to the rising rates of obesity and to difficulties in weight reduction that exist in the worldwide population. Caloric intake via sugar-sweetened beverages may be influential. This study tested the hypothesis that liquid sucrose intake promotes obesity by increasing serum insulin levels and tissue lipid accumulation.

methodsC57BL/6J mice were given 30% sucrose in liquid form. Changes in weight gain, body composition, energy expenditure (EE), and tissue lipid content were measured.

resultsMice drinking sucrose gained more total body mass (TBM), had greater fat mass, and displayed impaired glucose tolerance relative to control mice. These metabolic changes occurred without alterations in circulating insulin levels and despite increases in whole body EE. Lipid accrued in liver, but not skeletal muscle, of sucrose-consuming mice. Oxygen consumption (VO

conclusionsWeight gain induced by intake of liquid sucrose in mice is associated with lipid accrual in liver, but not skeletal muscle, and occurs without an increase in circulating insulin.

Indexed as

Administration, OralAnimalsBody CompositionBody WeightEnergy IntakeEnergy MetabolismGlucose IntoleranceInsulinLiverMaleMiceMice, Inbred C57BLMice, ObeseObesitySolutionsSucroseInsulinSolutionsSucroseSweetening Agents

Identifiers

PMID29901267
PMCPMC6014929
OpenAlexW2808090875

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.