Evidence map›Paper›PMID 31166222›Full record

ReviewCurrent opinion in clinical nutrition and metabolic care2019

Endogenous fructose production: what do we know and how relevant is it?

Ana Andres-Hernando, Richard J Johnson, Miguel A Lanaspa

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in clinical nutrition and metabolic care, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. New Insight Into Male Infertility: Deviation From Basic Tenets of Life.Oxidative medicine and cellular longevity · 2026
    Review
  3. Review
  4. Article
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  7. Article
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  10. Review
  11. Article
  12. Review
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  14. Review
  15. Fructose and the Liver.International journal of molecular sciences · 2021
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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

3 authors at 2 institutions in 1 country.

Ana Andres-HernandoDivision of Renal Diseases and Hypertension, University of Colorado AMC, Aurora, Colorado, USA.
Richard J Johnson
Miguel A Lanaspa
University of Colorado Denver · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Targeting fructokinase, endogenous fructose production and purine degradation for the prevention and treatment of hereditary fructose intoleranceR01DK108859 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Miguel Angel Lanaspa Garcia · 2016 to 2026
$2.4M
Novel Insulin-Independent Gluco-Regulatory MechanismsR01DK109408 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI BERGLUND, ERIC · 2016 to 2020
$1.8M
Dietary Salt has an Unrecognized Role in Modulating Energy Intake and Metabolic SyndromeR01DK108408 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI JOHNSON, RICHARD JOSEPH · 2016 to 2019
$1.6M
NIDDK NIH HHS R01 DK108408NIDDK NIH HHS R01 DK108859NIDDK NIH HHS R01 DK109408
6 · The paper itself

Abstract

purpose of reviewExcessive sugar and particularly fructose consumption has been proposed to be a key player in the pathogenesis of metabolic syndrome and kidney disease in humans and animal models. However, besides its dietary source, fructose can be endogenously produced in the body from glucose via the activation of the polyol pathway. In this review, we aim to describe the most recent findings and current knowledge on the potential role of endogenous fructose production and metabolism in disease. RECENT

findingsOver the recent years, the activation of the polyol pathway and endogenous fructose production has been observed in multiple tissues including the liver, renal cortex, and hypothalamic areas of the brain. The activation occurs during the development and progression of metabolic syndrome and kidney disease and results from different stimuli including osmotic effects, diabetes, and ischemia. Even though the potential toxicity of the activation of the polyol pathway can be attributed to several intermediate products, the blockade of endogenous fructose metabolism either by using fructokinase deficient mice or specific inhibitors resulted in marked amelioration of multiple metabolic diseases. SUMMARY: New findings suggest that fructose can be produced in the body and that the blockade of tis metabolism could be clinically relevant for the prevention and treatment of metabolic syndrome and kidney disease.

Indexed as

FructoseAnimalsDietary CarbohydratesFatty LiverFructokinasesHumansKidney DiseasesMetabolic DiseasesMetabolic Networks and PathwaysMicePolymersDietary CarbohydratesfructokinaseFructokinasesFructosePolymerspolyol

Identifiers

PMID31166222
PMCPMC6684314
OpenAlexW2945004015

What OpenQuestion holds

Textmetadata
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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.