Evidence map›Paper›PMID 30369316›Full record

ArticleJournal of the American Heart Association2018

Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol.

Cécile Low-Kam, David Rhainds, Ken Sin Lo, Amina Barhdadi, Marie Boulé, Sonia Alem, Valérie Pedneault-Gagnon, Eric Rhéaume, Marie-Pierre Dubé, David Busseuil and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
3.8field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. HDL Function across the Lifespan: From Childhood, to Pregnancy, to Old Age.International journal of molecular sciences · 2023
    Review
  8. Correlations between the NMR Lipoprotein Profile,International journal of molecular sciences · 2023
    Article
  9. Article
  10. Observational
  11. Observational
  12. Article
  13. Apolipoprotein E and Atherosclerosis.Current atherosclerosis reports · 2021
    Review
  14. Article
  15. COVID-19-Associated dyslipidemia: Implications for mechanism of impaired resolution and novel therapeutic approaches.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

13 authors at 2 institutions in 1 country.

Cécile Low-Kam1 Montreal Heart Institute Montréal Québec Canada.
David Rhainds1 Montreal Heart Institute Montréal Québec Canada.
Ken Sin Lo1 Montreal Heart Institute Montréal Québec Canada.
Amina Barhdadi1 Montreal Heart Institute Montréal Québec Canada.
Marie Boulé1 Montreal Heart Institute Montréal Québec Canada.
Sonia Alem1 Montreal Heart Institute Montréal Québec Canada.
Valérie Pedneault-Gagnon1 Montreal Heart Institute Montréal Québec Canada.
Eric Rhéaume1 Montreal Heart Institute Montréal Québec Canada.
Marie-Pierre Dubé1 Montreal Heart Institute Montréal Québec Canada.
David Busseuil1 Montreal Heart Institute Montréal Québec Canada.
Robert A Hegele2 Department of Biochemistry Robarts Research Institute Western University London Ontario Canada.
Guillaume Lettre1 Montreal Heart Institute Montréal Québec Canada.
Jean-Claude Tardif1 Montreal Heart Institute Montréal Québec Canada.
Montreal Heart Institute · CARobarts Clinical Trials · CA

Funding

CIHR MOP136979
6 · The paper itself

Abstract

Background Macrophage cholesterol efflux to high-density lipoproteins ( HDLs ) is the first step of reverse cholesterol transport. The cholesterol efflux capacity ( CEC ) of HDL particles is a protective risk factor for coronary artery disease independent of HDL cholesterol levels. Using a genome-wide association study approach, we aimed to identify pathways that regulate CEC in humans. Methods and Results We measured CEC in 5293 French Canadians. We tested the genetic association between 4 CEC measures and genotypes at >9 million common autosomal DNA sequence variants. These analyses yielded 10 genome-wide significant signals ( P<6.25×10

Indexed as

AgedApolipoprotein C-IApolipoprotein C-IIApolipoproteins CApolipoproteins ECanadaCase-Control StudiesCholesterolCholesterol, HDLCoronary Artery DiseaseFemaleGenetic VariationGenome-Wide Association StudyHumansMacrophagesMaleAPOC1 protein, humanAPOC4 protein, humanApolipoprotein C-IApolipoprotein C-IIApolipoproteins CApolipoproteins ECholesterolCholesterol, HDLgenome‐wide association studyHDL effluxhigh‐density lipoprotein cholesterol

Identifiers

PMID30369316
PMCPMC6201388
OpenAlexW2890357553

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.