Evidence map›Paper›PMID 33924948›Full record

ArticleMetabolites2021

In Vivo Estimation of Ketogenesis Using Metabolic Flux Analysis-Technical Aspects and Model Interpretation.

Stanislaw Deja, Blanka Kucejova, Xiaorong Fu, Jeffrey D Browning, Jamey D Young, Shawn Burgess

Abstract read
In one paragraph

Article in Metabolites, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Acetoacetate suppresses colon cancer via an MR1-MAIT axis.bioRxiv : the preprint server for biology · 2025
    Article
  3. Review
  4. Article
  5. Metabolic flux analysis in adipose tissue reprogramming.Immunometabolism (Cobham, Surrey) · 2024
    Review
  6. Article
  7. Review
  8. Review
  9. DetectingFrontiers in physiology · 2022
    Article
  10. Article
  11. 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

6 authors.

Stanislaw DejaCenter for Human Nutrition, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0002-7714-2547
Blanka KucejovaCenter for Human Nutrition, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0002-5058-330X
Xiaorong FuCenter for Human Nutrition, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0001-8042-4206
Jeffrey D BrowningDepartment of Clinical Nutrition, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Jamey D YoungDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN 37235, USA.ORCID 0000-0002-0871-1494
Shawn BurgessCenter for Human Nutrition, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

Funding

Factors controlling metabolic flux in the liver - Supplement RevisionR01DK078184 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Shawn C Burgess · 2008 to 2026
$6.8M
Regulation of lipogenesis by TCA cycle metabolismR01DK128168 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI BURGESS, SHAWN C · 2021 to 2025
$2.1M
In Vivo 2H/13C Metabolic Flux Analysis of NASH PathogenesisR01DK106348 · NIDDK · VANDERBILT UNIVERSITY · PI YOUNG, JAMEY D. · 2015 to 2019
$1.7M
National High Magnetic Field Laboratory P19414NIDDK NIH HHS R01 DK078184NIDDK NIH HHS R01 DK106348NIDDK NIH HHS R01 DK128168NIH HHS P41-EB-015908NIH HHS R01-DK078184Welch Foundation I-1804
6 · The paper itself

Abstract

Ketogenesis occurs in liver mitochondria where acetyl-CoA molecules, derived from lipid oxidation, are condensed into acetoacetate (AcAc) and reduced to β-hydroxybutyrate (BHB). During carbohydrate scarcity, these two ketones are released into circulation at high rates and used as oxidative fuels in peripheral tissues. Despite their physiological relevance and emerging roles in a variety of diseases, endogenous ketone production is rarely measured in vivo using tracer approaches. Accurate determination of this flux requires a two-pool model, simultaneous BHB and AcAc tracers, and special consideration for the stability of the AcAc tracer and analyte. We describe the implementation of a two-pool model using a metabolic flux analysis (MFA) approach that simultaneously regresses liquid chromatography-tandem mass spectrometry (LC-MS/MS) ketone isotopologues and tracer infusion rates. Additionally,

Indexed as

13C MFA1H NMRacetoacetateBHBfluxin vivoketogenesisLC-MS/MSlivermetabolismmetabolomicsstable isotope

Identifiers

PMID33924948
PMCPMC8146959

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Registered trials

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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.