Evidence map›Paper›PMID 40362449›Full record

ArticleInternational journal of molecular sciences2025

High-Protein Diet Prevents Glucocorticoid-Induced Fat Mass Accumulation and Hyperglycemia.

Susan J Burke, Heidi M Batdorf, Maggie P Ducote, Thomas M Martin, Michael D Karlstad, Robert C Noland, Sujoy Ghosh, Christopher D Morrison, J Jason Collier

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Susan J BurkeLaboratory of Immunogenetics, Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Heidi M BatdorfDepartment of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.
Maggie P DucoteLaboratory of Immunogenetics, Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Thomas M MartinLaboratory of Islet Biology and Inflammation, Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.ORCID 0009-0003-6574-0675
Michael D KarlstadDepartment of Surgery, Graduate School of Medicine, University of Tennessee Health Science Center, Knoxville, TN 37920, USA.
Robert C NolandSkeletal Muscle Metabolism Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.ORCID 0000-0001-5543-3450
Sujoy GhoshLaboratory of Computational Biology, Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.ORCID 0000-0002-7601-165X
Christopher D MorrisonLaboratory of Neurosignaling, Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.ORCID 0000-0002-5492-102X
J Jason CollierDepartment of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.ORCID 0000-0003-2817-4152

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
Mechanisms of glucocorticoid-induced metabolic dysfunction in skeletal muscleR56DK141177 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI COLLIER, JAMES JASON, NOLAND, ROBERT CHARLES · 2024 to 2024
$113k
NIH HHS P20 GM 135002NIH HHS P30 DK 072476NIH HHS R01 DK 123183NIH HHS R56 DK 141177NIH HHS S10 OD 023703
6 · The paper itself

Abstract

Glucocorticoid-induced diabetes is the most common form of drug-induced hyperglycemia. In addition, chronic exposure to glucocorticoids promotes lean mass loss and fat mass accumulation. In this study, we hypothesized that a high-protein diet (60% kcal; HPD) would help to offset sarcopenia during oral administration of corticosterone to C57BL/6J mice. Carbohydrates were reduced in the HPD to ensure it was isocaloric with the normal-protein diet (20% kcal; NPD). We found that the HPD prevented fat mass accumulation but did not protect against reductions in lean mass in both male and female mice. Mice consuming a HPD did not develop hyperglycemia, while mice given the NPD developed hyperglycemia within two weeks. The HPD diet did not improve insulin sensitivity in response to glucocorticoids but did alter gene expression patterns in adipose tissue and liver measured by RNA sequencing. We conclude that a HPD diet may be beneficial to limit rises in blood glucose and adipose tissue accrual during glucocorticoid therapy.

Indexed as

Adipose TissueDiet, High-ProteinGlucocorticoidsHyperglycemiaAnimalsBlood GlucoseCorticosteroneFemaleInsulin ResistanceLiverMaleMiceMice, Inbred C57BLBlood GlucoseCorticosteroneGlucocorticoidsdiabetesglucocorticoidsproteintranscriptomics

Identifiers

PMID40362449
PMCPMC12071877

What Socratic 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 Socratic graph.