Evidence map›Paper›PMID 26620373›Full record

Trial reportLipids2016

Docosahexaenoic Acid Attenuates Cardiovascular Risk Factors via a Decline in Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Plasma Levels.

Celia Rodríguez-Pérez, Vanu Ramkumar Ramprasath, Shuaihua Pu, Ali Sabra, Rosa Quirantes-Piné, Antonio Segura-Carretero, Peter J H Jones

Abstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Lipids, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. How lipids may affect risk for suicidal behavior.Journal of psychiatric research · 2018
    Review
  3. Review
  4. The American journal of clinical nutrition · 2017
    Article
  5. Article
  6. 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 4 institutions in 3 countries.

Celia Rodríguez-PérezDepartment of Analytical Chemistry, Faculty of Sciences, University of Granada, Avenida Fuentenueva s/n, 18071, Granada, Spain.
Vanu Ramkumar RamprasathDepartment of Human Nutritional Sciences, University of Manitoba, Winnipeg, MB, Canada.
Shuaihua PuDepartment of Human Nutritional Sciences, University of Manitoba, Winnipeg, MB, Canada.
Ali SabraRichardson Centre for Functional Foods and Nutraceuticals, Winnipeg, MB, Canada.
Rosa Quirantes-PinéResearch and Development Functional Food Centre (CIDAF), Health Science Technological Park, Avenida del Conocimiento, 37 Edificio BioRegión, 18016, Granada, Spain.
Antonio Segura-CarreteroDepartment of Analytical Chemistry, Faculty of Sciences, University of Granada, Avenida Fuentenueva s/n, 18071, Granada, Spain. ansegura@ugr.es.
Peter J H JonesDepartment of Human Nutritional Sciences, University of Manitoba, Winnipeg, MB, Canada.
Cargill (Canada) · CAUniversidad de Granada · ESUniversity of Manitoba · CAWeatherford College · US

Funding

TISSUE CULTURE COREP01HL049373 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SHELNESS, GREGORY S · 1993 to 2012
$23.8M
Penn State Clinical and Translational Science InstituteUL1TR000127 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SINOWAY, LAWRENCE I · 2012 to 2015
$17.1M
NCATS NIH HHS UL1TR000127NHLBI NIH HHS HL 49373
6 · The paper itself

Abstract

Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a circulating protein that regulates cholesterol metabolism by promoting LDL receptor degradation in the liver and has recently been proposed as a therapeutic target in the management of hyperlipidaemia. We investigated the impact of dietary fat on the metabolism of sterols and on plasma PCSK9 concentrations to explore likely clinical usefulness. In a post hoc analysis of a double-blind randomised crossover controlled feeding trial, the Canola Oil Multicenter Intervention Trial (COMIT), volunteers (n = 54) with at least one condition related to metabolic syndrome consumed diets with one of the following treatment oils in beverages: (1) conventional canola oil (Canola); (2) canola oil rich in docosahexanoic acid (DHA) (CanolaDHA); and (3) high-oleic acid canola oil (CanolaOleic). The enrichment in oleic acid resulted in lower plasma cholesterol concentration compared with diets enriched in DHA. Contrarily, DHA-enriched oil significantly decreased plasma PCSK9 and triacylglycerols levels, but increased circulating levels of sterols. The variations in lathosterol, sitosterol, and campesterol indicate that plasma PCSK9 levels are sensitive to changes in cholesterol synthesis and/or absorption. There was a significant correlation between plasma PCSK9 levels and plasma triacylglicerol and apolipoprotein B levels, which was not affected by dietary fat. Therefore, our results suggest that the impact of dietary fats should not be discarded as complementary treatment in the management of patients with hyperlipidaemia. These findings should be considered in the analysis of ongoing studies and may represent a cautionary note in the treatment of patients with cardiovascular risk.

Indexed as

AdultApolipoproteinsCardiovascular DiseasesCross-Over StudiesDietDocosahexaenoic AcidsDouble-Blind MethodEnergy IntakeFatty Acids, MonounsaturatedFemaleHumansMaleOleic AcidsProprotein Convertase 9Proprotein ConvertasesRapeseed OilApolipoproteinsDocosahexaenoic AcidsFatty Acids, MonounsaturatedOleic AcidsPCSK9 protein, humanProprotein Convertase 9Proprotein ConvertasesRapeseed OilSerine EndopeptidasesSterolsDocosahexaenoic acidFatty acidsHyperlipidaemiaPCSK9Sterols

Identifiers

PMID26620373
OpenAlexW2182832918

What OpenQuestion holds

Texttitle and abstract
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.