Evidence map›Paper›PMID 26604176›Full record

ReviewDiabetes2015

Measurements of Gluconeogenesis and Glycogenolysis: A Methodological Review.

Stephanie T Chung, Shaji K Chacko, Agneta L Sunehag, Morey W Haymond

Open access · bronzeAbstract readReview
In one paragraph

Review in Diabetes, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

45 citing papers in PubMed, 85 citations in OpenAlex.

  1. Trial
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  3. Review
  4. Article
  5. Review
  6. Proximal Tubule-Specific Genetic Deficiency of PPARα Worsens Systemic Lipid and Glucose Metabolism During Fasting.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  7. Dynamic expression of the zebrafish (Danio rerio) proteome across early larval development.Comparative biochemistry and physiology. Part D, Genomics & proteomics · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
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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

4 authors at 3 institutions in 1 country.

Stephanie T ChungNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.
Shaji K ChackoU.S. Department of Agriculture/Agricultural Research Service Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX.
Agneta L SunehagU.S. Department of Agriculture/Agricultural Research Service Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX.
Morey W HaymondU.S. Department of Agriculture/Agricultural Research Service Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX mhaymond@bcm.edu.
Agricultural Research Service · USChildren's Nutrition Research Center at Baylor College of Medicine · USNational Institute of Diabetes and Digestive and Kidney Diseases · US

Funding

METABOLIC ADAPTATION AND CONTROL OF LACTATION IN HUMANSR01DK055478 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI HAYMOND, MOREY W · 1999 to 2010
$2.7M
Glucose &Lipid Metabolism in Obese AdolescentsR01HD044609 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI SUNEHAG, AGNETA LISBETH · 2005 to 2009
$2.3M
Regulation of Glucose Metabolism in Extremely Low Birth Weight (ELBW) InfantsR01HD037957 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI SUNEHAG, AGNETA LISBETH · 2000 to 2010
$2.3M
Nested Study: Identifying Risk for Diabetes and Heart Disease in Women: A Study of African-American, African and White Federal Employees and ContractorsZIADK075105 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI CHUNG, STEPHANIE THERESE · 2014 to 2025
$1.8M
Baylor Pediatric Diabetes Research Training ProgramT32DK063873 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI HAYMOND, MOREY W · 2002 to 2011
$1.3M
NICHD NIH HHS 1R01-HD-044609NICHD NIH HHS 2R01-HD-037957NICHD NIH HHS R01 HD037957NICHD NIH HHS R01 HD044609NIDDK NIH HHS 5R01-DK-055478NIDDK NIH HHS 5T32-DK-063873NIDDK NIH HHS R01 DK055478NIDDK NIH HHS T32 DK063873
6 · The paper itself

Abstract

Gluconeogenesis is a complex metabolic process that involves multiple enzymatic steps regulated by myriad factors, including substrate concentrations, the redox state, activation and inhibition of specific enzyme steps, and hormonal modulation. At present, the most widely accepted technique to determine gluconeogenesis is by measuring the incorporation of deuterium from the body water pool into newly formed glucose. However, several techniques using radioactive and stable-labeled isotopes have been used to quantitate the contribution and regulation of gluconeogenesis in humans. Each method has its advantages, methodological assumptions, and set of propagated errors. In this review, we examine the strengths and weaknesses of the most commonly used stable isotopes methods to measure gluconeogenesis in vivo. We discuss the advantages and limitations of each method and summarize the applicability of these measurements in understanding normal and pathophysiological conditions.

Indexed as

Biomedical ResearchEvidence-Based MedicineGluconeogenesisGlycogenolysisModels, BiologicalAnimalsHumansKidneyLiver

Identifiers

PMID26604176
PMCPMC4657587
OpenAlexW2178272958

What Socratic holds

Textmetadata
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.