Evidence map›Paper›PMID 32750298›Full record

ArticleJournal of the American Heart Association2020

Increased Glucose Availability Attenuates Myocardial Ketone Body Utilization.

Manoja K Brahma, Chae-Myeong Ha, Mark E Pepin, Sobuj Mia, Zhihuan Sun, John C Chatham, Kirk M Habegger, Evan Dale Abel, Andrew J Paterson, Martin E Young and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

51 citing papers in PubMed, 66 citations in OpenAlex.

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  17. Post-translational modifications in diabetic cardiomyopathy.Journal of cellular and molecular medicine · 2024
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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

11 authors at 2 institutions in 1 country.

Manoja K BrahmaDepartments of Pathology Division of Molecular and Cellular Pathology University of Alabama at Birmingham AL USA.
Chae-Myeong HaDepartments of Pathology Division of Molecular and Cellular Pathology University of Alabama at Birmingham AL USA.
Mark E PepinDepartments of Pathology Division of Molecular and Cellular Pathology University of Alabama at Birmingham AL USA.
Sobuj MiaMedicine, Division of Cardiovascular Diseases University of Alabama at Birmingham AL USA.
Zhihuan SunDepartments of Pathology Division of Molecular and Cellular Pathology University of Alabama at Birmingham AL USA.
John C ChathamDepartments of Pathology Division of Molecular and Cellular Pathology University of Alabama at Birmingham AL USA.
Kirk M HabeggerMedicine, Division of Endocrinology, Diabetes, and Metabolism University of Alabama at Birmingham AL USA.
Evan Dale AbelFraternal Order of Eagles Diabetes Research Center and Division of Endocrinology and Metabolism Carver College of MedicineUniversity of Iowa Iowa City IA USA.
Andrew J PatersonMedicine, Division of Endocrinology, Diabetes, and Metabolism University of Alabama at Birmingham AL USA.
Martin E YoungMedicine, Division of Cardiovascular Diseases University of Alabama at Birmingham AL USA.
Adam R WendeDepartments of Pathology Division of Molecular and Cellular Pathology University of Alabama at Birmingham AL USA.
University of Alabama at Birmingham · USUniversity of Iowa · US

Funding

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
Modeling Diabetic Cardiomyopathy and Microangiopathy U01HL087947 · NHLBI · UNIVERSITY OF UTAH · PI ABEL, E DALE · 2006 to 2010
$1.8M
Glucose-Mediated Remodeling of Cardiac DNA MethylationR01HL133011 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WENDE, ADAM RAYMOND · 2017 to 2020
$1.5M
Insulin Resistance and Myocardial AutophagyR01HL108379 · NHLBI · UNIVERSITY OF UTAH · PI ABEL, E DALE · 2011 to 2014
$1.5M
Mechanisms of glucose mediated cardiac mitochondrial dysfunctionR00HL111322 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WENDE, ADAM RAYMOND · 2013 to 2015
$870k
Insulin Signaling and the Heart in DiabetesR01DK092065 · NIDDK · UNIVERSITY OF UTAH · PI ABEL, E DALE · 2010 to 2011
$649k
GADD45B and Metabolic Memory in Diabetic Heart FailureF30HL137240 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PEPIN, MARK EMILE · 2018 to 2019
$83k
NHLBI NIH HHS F30 HL137240NHLBI NIH HHS R00 HL111322NHLBI NIH HHS R01 HL108379NHLBI NIH HHS R01 HL133011NHLBI NIH HHS U01 HL087947NIDDK NIH HHS P30 DK056336NIDDK NIH HHS P30 DK079626NIDDK NIH HHS R01 DK092065
6 · The paper itself

Abstract

Background Perturbations in myocardial substrate utilization have been proposed to contribute to the pathogenesis of cardiac dysfunction in diabetic subjects. The failing heart in nondiabetics tends to decrease reliance on fatty acid and glucose oxidation, and increases reliance on ketone body oxidation. In contrast, little is known regarding the mechanisms mediating this shift among all 3 substrates in diabetes mellitus. Therefore, we tested the hypothesis that changes in myocardial glucose utilization directly influence ketone body catabolism. Methods and Results We examined ventricular-cardiac tissue from the following murine models: (1) streptozotocin-induced type 1 diabetes mellitus; (2) high-fat-diet-induced glucose intolerance; and transgenic inducible cardiac-restricted expression of (3) glucose transporter 4 (transgenic inducible cardiac restricted expression of glucose transporter 4); or (4) dominant negative

Indexed as

AnimalsBlotting, WesternDiabetes Mellitus, ExperimentalGlucoseGlucose IntoleranceGlucose Transporter Type 4ImmunoprecipitationKetone BodiesMaleMiceMyocardiumMyocytes, CardiacReal-Time Polymerase Chain ReactionSequence Analysis, RNAGlucoseGlucose Transporter Type 4Ketone BodiesSlc2a4 protein, mousecardiomyopathydiabetes mellitusdiabetic cardiomyopathyglucoseketone metabolismmitochondriaO‐GlcNAcylation

Identifiers

PMID32750298
PMCPMC7792234
OpenAlexW3045572344

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.