Evidence map›Paper›PMID 36105576›Full record

ArticleFrontiers in nutrition2022

A modified standard American diet induces physiological parameters associated with metabolic syndrome in C57BL/6J mice.

Sophie B Chehade, George B H Green, Christopher D Graham, Ayanabha Chakraborti, Bijal Vashai, Amber Moon, Michael B Williams, Benjamin Vickers, Taylor Berryhill, William Van Der Pol and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in nutrition, 2022. 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
0.2field-weighted citation impact, top 47% 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.

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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

19 authors at 1 institution in 1 country.

Sophie B ChehadeDepartment of Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
George B H GreenDepartment of Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
Christopher D GrahamDepartment of Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
Ayanabha ChakrabortiDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Bijal VashaiDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Amber MoonDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Michael B WilliamsDepartment of Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
Benjamin VickersDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Taylor BerryhillComprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, United States.
William Van Der PolCenter for Clinical and Translational Science, University of Alabama at Birmingham, Birmingham, AL, United States.
Landon WilsonDepartment of Pharmacology and Toxicology, University of Alabama at Birmingham, Birmingham, AL, United States.
Mickie L PowellDepartment of Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
Daniel L SmithDepartment of Nutrition Sciences, Nutrition Obesity Research Center, University of Alabama at Birmingham, Birmingham, AL, United States.
Stephen BarnesComprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, United States.
Casey MorrowDepartment of Cell, Developmental, and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
M Shahid MukhtarDepartment of Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
Gregory D KennedyDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
James A BibbDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Stephen A WattsDepartment of Biology, University of Alabama at Birmingham, Birmingham, AL, United States.
University of Alabama at Birmingham · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Why is the prevalence of obesity so high in U.S. Southern States? Regional predictors of BMI and obesity treatment response.P30DK056336 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BARBARA A GOWER · 2000 to 2026
$31.9M
University of Alabama at Birmingham's Diabetes Research CenterP30DK079626 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Kirk Michael Habegger · 2013 to 2026
$19.5M
PERIPHERAL INFLAMMATION AND STRESS DRIVE VENTRAL STRIATAL MALADAPTATIONSR01MH126948 · NIMH · UNIVERSITY OF ARIZONA · PI BIBB, JAMES A · 2021 to 2025
$2.5M
Excitatory and Metabotopic Regulation of PKA in Stress and ResilienceR01MH116896 · NIMH · UNIVERSITY OF ARIZONA · PI BIBB, JAMES A · 2019 to 2022
$1.5M
NCI NIH HHS P30 CA013148NIDDK NIH HHS P30 DK056336NIDDK NIH HHS P30 DK079626NIMH NIH HHS R01 MH116896NIMH NIH HHS R01 MH126948
6 · The paper itself

Abstract

Investigations into the causative role that western dietary patterns have on obesity and disease pathogenesis have speculated that quality and quantity of dietary fats and/or carbohydrates have a predictive role in the development of these disorders. Standard reference diets such as the AIN-93 rodent diet have historically been used to promote animal health and reduce variation of results across experiments, rather than model modern human dietary habits or nutrition-related pathologies. In rodents high-fat diets (HFDs) became a classic tool to investigate diet-induced obesity (DIO). These murine diets often relied on a single fat source with the most DIO consistent HFDs containing levels of fat up to 45-60% (kcal), higher than the reported human intake of 33-35% (kcal). More recently, researchers are formulating experimental animal (pre-clinical) diets that reflect mean human macro- and micronutrient consumption levels described by the National Health and Nutrition Examination Survey (NHANES). These diets attempt to integrate relevant ingredient sources and levels of nutrients; however, they most often fail to include high-fructose corn syrup (HFCS) as a source of dietary carbohydrate. We have formulated a modified Standard American Diet (mSAD) that incorporates relevant levels and sources of nutrient classes, including dietary HFCS, to assess the basal physiologies associated with mSAD consumption. Mice proffered the mSAD for 15 weeks displayed a phenotype consistent with metabolic syndrome, exhibiting increased adiposity, fasting hyperglycemia with impaired glucose and insulin tolerance. Metabolic alterations were evidenced at the tissue level as crown-like structures (CLS) in adipose tissue and fatty acid deposition in the liver, and targeted 16S rRNA metagenomics revealed microbial compositional shifts between dietary groups. This study suggests diet quality significantly affects metabolic homeostasis, emphasizing the importance of developing relevant pre-clinical diets to investigate chronic diseases highly impacted by western dietary consumption patterns.

Indexed as

high fat diethigh fructose corn syrupmetabolic syndromeobesityWestern Diet

Identifiers

PMID36105576
PMCPMC9464921
OpenAlexW4293418561

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.