Evidence mapPaperPMID 28294174Full record

Trial reportEuropean journal of clinical nutrition2017

Docosahexaenoic acid enrichment in NAFLD is associated with improvements in hepatic metabolism and hepatic insulin sensitivity: a pilot study.

L Hodson, L Bhatia, E Scorletti, D E Smith, N C Jackson, F Shojaee-Moradie, M Umpleby, P C Calder, C D Byrne

Erratum issuedOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in European journal of clinical nutrition, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 4 pooled it
6.0field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 4 syntheses or guidelines pooled it, 63 citations in OpenAlex.

  1. Pooled it
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  18. Dietary carbohydrates and fats in nonalcoholic fatty liver disease.Nature reviews. Gastroenterology & hepatology · 2021
    Review
  19. Nutrients · 2021
    Article
  20. DHA Suppresses Hepatic Lipid AccumulationFrontiers in nutrition · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 1 country.

L HodsonOxford Centre for Diabetes, Endocrinology and Metabolism (OCDEM), Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
L BhatiaHuman Development and Health Academic Unit, Southampton, UK.
E ScorlettiHuman Development and Health Academic Unit, Southampton, UK.
D E SmithHuman Development and Health Academic Unit, Southampton, UK.
N C JacksonDiabetes and Metabolic Medicine, Department of Nutritional Sciences, University of Surrey, Guildford, UK.
F Shojaee-MoradieDiabetes and Metabolic Medicine, Department of Nutritional Sciences, University of Surrey, Guildford, UK.
M UmplebyDiabetes and Metabolic Medicine, Department of Nutritional Sciences, University of Surrey, Guildford, UK.
P C CalderHuman Development and Health Academic Unit, Southampton, UK.
C D ByrneHuman Development and Health Academic Unit, Southampton, UK.
University of Surrey · GBUniversity of Southampton · GBNIHR Southampton Biomedical Research Centre · GBOxford Centre for Diabetes, Endocrinology and Metabolism · GBUniversity Hospital Southampton NHS Foundation Trust · GB

Funding

British Heart Foundation FS/11/18/28633Department of Health SOUBRC-1Diabetes UK 11/0004337
6 · The paper itself

Abstract

BACKGROUND/

objectiveTreatment of subjects with non-alcoholic fatty liver disease (NAFLD) with omega-3 polyunsaturated fatty acids (FAs) suggests high levels of docosahexaenoic acid (DHA) tissue enrichment decrease liver fat content. We assessed whether changes in erythrocyte DHA enrichment (as a surrogate marker of changes in tissue enrichment) were associated with alterations in hepatic de novo lipogenesis (DNL), postprandial FA partitioning and hepatic and peripheral insulin sensitivity in a sub-study of the WELCOME trial (Wessex Evaluation of fatty Liver and Cardiovascular markers in NAFLD (non-alcoholic fatty liver disease) with OMacor thErapy). SUBJECTS/

methodsSixteen participants were randomised to 4 g/day EPA+DHA (n=8) or placebo (n=8) for 15-18 months and underwent pre- and post-intervention measurements. Fasting and postprandial hepatic FA metabolism was assessed using metabolic substrates labelled with stable-isotope tracers (

resultsNine participants were stratified to DHA⩾2% (eight randomised to EPA+DHA and one to placebo) and seven to the DHA<2% group (all placebo). Compared with individuals with erythrocyte <2% change in DHA abundance, those with ⩾2% enrichment had significant improvements in hepatic insulin sensitivity, reduced fasting and postprandial plasma triglyceride concentrations, decreased fasting hepatic DNL, as well as greater appearance of

conclusionsThe findings from our pilot study indicate that individuals who achieved a change in erythrocyte DHA enrichment ⩾2% show favourable changes in hepatic FA metabolism and insulin sensitivity, which may contribute to decreasing hepatic fat content.

Indexed as

Dietary SupplementsInsulin ResistanceLipid Metabolism3-Hydroxybutyric AcidAdultBiomarkersCohort StudiesDocosahexaenoic AcidsDouble-Blind MethodEicosapentaenoic AcidErythrocytesFemaleHumansLipogenesisLiverMale3-Hydroxybutyric AcidBiomarkersDocosahexaenoic AcidsEicosapentaenoic Acid

Identifiers

PMID28294174
PMCPMC5474320
OpenAlexW2596220060

What Socratic holds

Textmetadata
LicenceCC BY
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.