Evidence map›Paper›PMID 26136510›Full record

ArticleJournal of lipid research2015

The n-3 long-chain PUFAs modulate the impact of the GCKR Pro446Leu polymorphism on triglycerides in adolescents.

Julien Rousseaux, Alain Duhamel, Julie Dumont, Jean Dallongeville, Denes Molnar, Kurt Widhalm, Yannis Manios, Michael Sjöström, Anthony Kafatos, Christina Breidenassel and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 27% 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

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

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. 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

18 authors at 15 institutions in 8 countries.

Julien RousseauxInserm U995, LIRIC, CHU Lille, University Lille, Lille, France Unité de Biostatistiques, CERIM, EA2694, CHU Lille, University Lille, Lille, France.
Alain DuhamelUnité de Biostatistiques, CERIM, EA2694, CHU Lille, University Lille, Lille, France.
Julie DumontInserm UMR1167, Institut Pasteur de Lille, University Lille, Lille, France.
Jean DallongevilleInserm UMR1167, Institut Pasteur de Lille, University Lille, Lille, France.
Denes MolnarDepartment of Pediatrics, University of Pécs, Pécs, Hungary.
Kurt WidhalmAcademic Institute for Clinical Nutrition, Vienna, Austria and Private Medical University Salzburg, Salzburg, Austria.
Yannis ManiosDepartment of Nutrition and Dietetics, Harokopio University, Athens, Greece.
Michael SjöströmUnit for Preventive Nutrition, Department of Biosciences and Nutrition, Karolinska Institute, Huddinge, Sweden.
Anthony KafatosPreventive Medicine and Nutrition Unit, School of Medicine, University of Crete, Heraklion, Greece.
Christina BreidenasselInstitut für Ernährungs-und Lebensmittelwissenschaften, Humanernährung, Rheinische Friedrich-Wilhelms, Universität Bonn, Bonn, Germany.
Marcela Gonzales-GrossFacultad de la Actividad Física y del Deporte-INEF, Universidad Politécnica de Madrid, Madrid, Spain.
Magdalena Cuenca-GarciaDepartment of Medical Physiology, Faculty of Medicine, Granada University, Granada, Spain.
Laura CensiNational Research Institute on Food and Nutrition, Rome, Italy.
Marcos AscensiónImmunonutrition Research Group, Department of Metabolism and Nutrition, Institute of Food Science and Technology and Nutrition (ICTAN-CSIC), Madrid, Spain.
Stefaan De HenauwDepartment of Public Health, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
Luis A MorenoGENUD (Growth, Exercise, Nutrition and Development) Research Group, Escuela Universitaria de Ciencias de la Salud, Universidad de Zaragoza, Zaragoza, Spain.
Aline MeirhaegheInserm UMR1167, Institut Pasteur de Lille, University Lille, Lille, France.
Frédéric GottrandInserm U995, LIRIC, CHU Lille, University Lille, Lille, France.
Inserm · FRGhent University · BEHarokopio University of Athens · GRInstituto de Ciencia y Tecnología de Alimentos y Nutrición · ESInstitut Pasteur de Lille · FRIstituto Nazionale di Ricerca per gli Alimenti e la Nutrizione · ITKarolinska Institutet · SELille Inflammation Research International Center · FRUniversidad de Granada · ESUniversidad de Zaragoza · ESUniversidad Politécnica de Madrid · ESUniversité de Lille · FRUniversity of Bonn · DEUniversity of Crete · GRUniversity of Pecs · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dietary n-3 long-chain PUFAs (LC-PUFAs) are associated with improvement in the parameters of the metabolic syndrome (MetS). Glucokinase regulatory protein (GCKR) is a key protein regulating intracellular glucose disposal. Our aim was to investigate: i) the relationship between the GCKR rs1260326 (Pro446Leu) polymorphism and parameters of the MetS; and ii) a potential influence of n-3 and n-6 LC-PUFA levels on this relationship in the HELENA study (1,155 European adolescents). Linear regression analyses were performed to study the association between rs1260326 and the outcomes of interest. Interactions between rs1260326 and LC-PUFA levels on outcomes were explored. The T allele of rs1260326 was associated with higher serum TG concentrations compared with the C allele. In contrast to n-6 LC-PUFA levels, a significant interaction (P = 0.01) between rs1260326 and total n-3 LC-PUFA levels on serum TG concentrations was observed. After stratification on the n-3 LC-PUFA median values, the association between rs1260326 and TG concentration was significant only in the group with high n-3 LC-PUFA levels. In conclusion, this is the first evidence that n-3 LC-PUFAs may modulate the impact of the GCKR rs1260326 polymorphism on TG concentrations in adolescents. Several molecular mechanisms, in link with glucose uptake, could explain these findings.

Indexed as

Adaptor Proteins, Signal TransducingAdolescentFatty Acids, Omega-3FemaleGenetic Association StudiesGlucoseHumansLipid MetabolismMaleMetabolic SyndromePolymorphism, Single NucleotideTriglyceridesAdaptor Proteins, Signal TransducingFatty Acids, Omega-3GCKR protein, humanGlucoseTriglyceridesglucokinase regulatory proteinlipid metabolismpolyunsaturated fatty acid

Identifiers

PMID26136510
PMCPMC4548781
OpenAlexW2255116566

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.