Evidence map›Paper›PMID 30869790›Full record

ArticleThe Journal of clinical endocrinology and metabolism2019

Isocaloric Fructose Restriction Reduces Serum d-Lactate Concentration in Children With Obesity and Metabolic Syndrome.

Ayca Erkin-Cakmak, Yasmin Bains, Russell Caccavello, Susan M Noworolski, Jean-Marc Schwarz, Kathleen Mulligan, Robert H Lustig, Alejandro Gugliucci

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
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  12. Sugar and Dyslipidemia: A Double-Hit, Perfect Storm.Journal of clinical medicine · 2023
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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

8 authors at 2 institutions in 1 country.

Ayca Erkin-CakmakDivision of Pediatric Endocrinology, Department of Pediatrics, University of California San Francisco, San Francisco, California.
Yasmin BainsGlycation, Oxidation and Disease Laboratory, Department of Research, Touro University California College of Osteopathic Medicine, Vallejo, California.
Russell CaccavelloGlycation, Oxidation and Disease Laboratory, Department of Research, Touro University California College of Osteopathic Medicine, Vallejo, California.
Susan M NoworolskiDepartment of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California.
Jean-Marc SchwarzDivision of Endocrinology, Department of Medicine, University of California San Francisco, San Francisco, California.
Kathleen MulliganDivision of Endocrinology, Department of Medicine, University of California San Francisco, San Francisco, California.
Robert H LustigDivision of Pediatric Endocrinology, Department of Pediatrics, University of California San Francisco, San Francisco, California.
Alejandro GugliucciGlycation, Oxidation and Disease Laboratory, Department of Research, Touro University California College of Osteopathic Medicine, Vallejo, California.
University of California, San Francisco · USTouro University California · US

Funding

Engaging University of California Stakeholders for Biorespository ResearchUL1TR000004 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRANDIS, JENNIFER RUBIN · 2012 to 2015
$78.0M
Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Brian N Finck · 1999 to 2026
$30.2M
UCSF Nutrition Obesity Research CenterP30DK098722 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHRISTIAN VAISSE · 2015 to 2026
$14.6M
Training Program in Pediatric EndocrinologyT32DK007161 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Brian J Feldman, STEPHEN E GITELMAN · 1986 to 2026
$6.2M
Metabolic impact of fructose restriction in obese childrenR01DK089216 · NIDDK · TOURO UNIVERSITY OF CALIFORNIA · PI LUSTIG, ROBERT H, SCHWARZ, JEAN-MARC · 2010 to 2014
$2.9M
NCATS NIH HHS UL1 TR000004NIDDK NIH HHS P30 DK056341NIDDK NIH HHS P30 DK098722NIDDK NIH HHS R01 DK089216NIDDK NIH HHS T32 DK007161
6 · The paper itself

Abstract

objectiveTo investigate the link between dietary sugar consumption and two separate pathogenetic mechanisms associated with metabolic syndrome: de novo lipogenesis (DNL) and nonenzymatic glycation. DESIGN AND

participantsWe assessed changes in serum d-lactate (the detoxification end-product of methylglyoxal) concentration in response to 9 days of isocaloric fructose restriction in 20 children with obesity and metabolic syndrome, and examined correlations with changes in DNL, liver fat, insulin sensitivity, and other metrics of hepatic metabolism.

interventionsNine days of dietary sugar restriction, with substitution of equal amounts of refined starch.

main outcome measuresOn days 0 and 10, children had laboratory evaluation of d-lactate levels and other analytes, and underwent oral glucose tolerance testing, magnetic resonance spectroscopy to quantify fat depots, and 13C-acetate incorporation into triglyceride (TG) to measure DNL.

resultsd-Lactate was associated with baseline liver fat fraction (P < 0.001) and visceral adipose tissue (P < 0.001) but not with subcutaneous adipose tissue. At baseline, d-lactate was positively correlated with DNL-area under the curve (AUC) (P = 0.003), liver fat fraction (P = 0.02), TG (P = 0.004), and TG/high-density lipoprotein ratio (P = 0.002). After 9 days of isocaloric fructose restriction, serum d-lactate levels reduced by 50% (P < 0.0001), and changes in d-lactate correlated with both changes in DNL-AUC and measures of insulin sensitivity.

conclusionBaseline correlation of d-lactate with DNL and measures of insulin sensitivity and reduction in d-lactate after 9 days of isocaloric fructose restriction suggest that DNL and nonenzymatic glycation are functionally linked via intermediary glycolysis in the pathogenesis of metabolic syndrome and point to fructose as a key dietary substrate that drives both pathways.

Indexed as

Dietary SugarsFructoseInsulin ResistanceLipogenesisAdipose TissueAdolescentBlack or African AmericanCarbon-13 Magnetic Resonance SpectroscopyChildDietary CarbohydratesFemaleGlucose Tolerance TestHispanic or LatinoHumansLactic AcidLiverDietary CarbohydratesDietary SugarsFructoseLactic AcidPyruvaldehydeTriglycerides

Identifiers

PMID30869790
PMCPMC6553815
OpenAlexW2921577147

What OpenQuestion 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 OpenQuestion graph.