Evidence map›Paper›PMID 22733000›Full record

Trial reportEuropean journal of nutrition2013

Adaptive metabolic response to 4 weeks of sugar-sweetened beverage consumption in healthy, lightly active individuals and chronic high glucose availability in primary human myotubes.

Francesco Sartor, Matthew J Jackson, Cesare Squillace, Anthony Shepherd, Jonathan P Moore, Donald E Ayer, Hans-Peter Kubis

Abstract readClinical Trial
In one paragraph

Trial report in European journal of nutrition, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 37% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Impact of dietary glycemic challenge on fuel partitioning.European journal of clinical nutrition · 2017
    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

7 authors at 3 institutions in 3 countries.

Francesco SartorCollege of Health and Behavioural Sciences, Bangor University, George Building, Bangor, Gwynedd, LL57 2PZ, UK.
Matthew J Jackson
Cesare Squillace
Anthony Shepherd
Jonathan P Moore
Donald E Ayer
Hans-Peter Kubis
Bangor University · GBUniversity of Urbino · ITUniversity of Utah · US

Funding

Nutrient Sensing and Growth ControlR01GM055668 · NIGMS · UNIVERSITY OF UTAH · PI AYER, DONALD E · 1997 to 2015
$4.3M
NIGMS NIH HHS R01 GM055668
6 · The paper itself

Abstract

purposeChronic sugar-sweetened beverage (SSB) consumption is associated with obesity and type 2 diabetes mellitus (T2DM). Hyperglycaemia contributes to metabolic alterations observed in T2DM, such as reduced oxidative capacity and elevated glycolytic and lipogenic enzyme expressions in skeletal muscle tissue. We aimed to investigate the metabolic alterations induced by SSB supplementation in healthy individuals and to compare these with the effects of chronic hyperglycaemia on primary muscle cell cultures.

methodsLightly active, healthy, lean subjects (n = 11) with sporadic soft drink consumption underwent a 4-week SSB supplementation (140 ± 15 g/day, ~2 g glucose/kg body weight/day, glucose syrup). Before and after the intervention, body composition, respiratory exchange ratio (RER), insulin sensitivity, muscle metabolic gene and protein expression were assessed. Adaptive responses to hyperglycaemia (7 days, 15 mM) were tested in primary human myotubes.

resultsSSB supplementation increased fat mass (+1.0 kg, P < 0.05), fasting RER (+0.12, P < 0.05), fasting glucose (+0.3 mmol/L, P < 0.05) and muscle GAPDH mRNA expressions (+0.94 AU, P < 0.05). PGC1α mRNA was reduced (-0.20 AU, P < 0.05). Trends were found for insulin resistance (+0.16 mU/L, P = 0.09), and MondoA protein levels (+1.58 AU, P = 0.08). Primary myotubes showed elevations in GAPDH, ACC, MondoA and TXNIP protein expressions (P < 0.05).

conclusionFour weeks of SSB supplementation in healthy individuals shifted substrate metabolism towards carbohydrates, increasing glycolytic and lipogenic gene expression and reducing mitochondrial markers. Glucose-sensing protein MondoA might contribute to this shift, although further in vivo evidence is needed to corroborate this.

Indexed as

Gene Expression RegulationAcetyl-CoA CarboxylaseAdipose TissueAdultBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsBody CompositionCarbonated BeveragesCarrier ProteinsCells, CulturedEnergy DrinksFemaleGlucoseGlyceraldehyde-3-Phosphate DehydrogenasesHeat-Shock ProteinsHumansHyperglycemiaAcetyl-CoA CarboxylaseBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCarrier ProteinsGlucoseGlyceraldehyde-3-Phosphate DehydrogenasesHeat-Shock ProteinsMLXIP protein, humanPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPARGC1A protein, humanTranscription FactorsTXNIP protein, human

Identifiers

PMID22733000
PMCPMC4447301
OpenAlexW2076938683

What OpenQuestion holds

Textmetadata
LicenceTDM
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.