Evidence map›Paper›PMID 38931176›Full record

ArticleNutrients2024

The Metabolic and Endocrine Effects of a 12-Week Allulose-Rich Diet.

Kevin B Cayabyab, Marley J Shin, Micah S Heimuli, Iris J Kim, Dominic P D'Agostino, Richard J Johnson, Andrew P Koutnik, Nick Bellissimo, David M Diamond, Nicholas G Norwitz and 3 more

Abstract read
In one paragraph

Article in Nutrients, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
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

13 authors.

Kevin B CayabyabDepartment of Cell Biology and Physiology, Brigham Young University, Provo, UT 84602, USA.
Marley J ShinDepartment of Cell Biology and Physiology, Brigham Young University, Provo, UT 84602, USA.
Micah S HeimuliDepartment of Cell Biology and Physiology, Brigham Young University, Provo, UT 84602, USA.
Iris J KimDepartment of Cell Biology and Physiology, Brigham Young University, Provo, UT 84602, USA.
Dominic P D'AgostinoDepartment of Molecular Pharmacology and Physiology, University of South Florida, Tampa, FL 33602, USA.ORCID 0000-0001-9652-181X
Richard J JohnsonDepartment of Medicine, University of Colorado, Aurora, CO 80045, USA.
Andrew P KoutnikSansum Diabetes Research Institute, Santa Barbara, CA 93105, USA.
Nick BellissimoSchool of Nutrition, Toronto Metropolitan University, Toronto, ON M5S 1A8, Canada.
David M DiamondDepartment of Psychology, University of South Florida, Tampa, FL 33602, USA.ORCID 0000-0003-4155-8687
Nicholas G NorwitzHarvard Medical School, Boston, MA 02115, USA.
Juan A ArroyoDepartment of Cell Biology and Physiology, Brigham Young University, Provo, UT 84602, USA.
Paul R ReynoldsDepartment of Cell Biology and Physiology, Brigham Young University, Provo, UT 84602, USA.ORCID 0000-0002-0931-3025
Benjamin T BikmanDepartment of Cell Biology and Physiology, Brigham Young University, Provo, UT 84602, USA.

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Wendy M Kohrt · 1995 to 2026
$32.6M
Anderson Advanced Ingredients R0602714
6 · The paper itself

Abstract

The global rise in type 2 diabetes (T2D) and obesity necessitates innovative dietary interventions. This study investigates the effects of allulose, a rare sugar shown to reduce blood glucose, in a rat model of diet-induced obesity and T2D. Over 12 weeks, we hypothesized that allulose supplementation would improve body weight, insulin sensitivity, and glycemic control. Our results showed that allulose mitigated the adverse effects of high-fat, high-sugar diets, including reduced body weight gain and improved insulin resistance. The allulose group exhibited lower food consumption and increased levels of glucagon-like peptide-1 (GLP-1), enhancing glucose regulation and appetite control. Additionally, allulose prevented liver triglyceride accumulation and promoted mitochondrial uncoupling in adipose tissue. These findings suggest that allulose supplementation can improve metabolic health markers, making it a promising dietary component for managing obesity and T2D. Further research is needed to explore the long-term benefits and mechanisms of allulose in metabolic disease prevention and management. This study supports the potential of allulose as a safe and effective intervention for improving metabolic health in the context of dietary excess.

Indexed as

Blood GlucoseDiabetes Mellitus, Type 2Diet, High-FatFructoseInsulin ResistanceObesityAdipose TissueAnimalsDisease Models, AnimalGlucagon-Like Peptide 1LiverMaleRatsRats, Sprague-DawleyTriglyceridesWeight GainBlood GlucoseFructoseGlucagon-Like Peptide 1psicoseTriglyceridesallulosediabetesinsulin resistancemitochondriaobesity

Identifiers

PMID38931176
PMCPMC11207032

What OpenQuestion holds

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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.