Evidence map›Paper›PMID 23842142›Full record

ReviewCurrent opinion in lipidology2013

New developments in selective cholesteryl ester uptake.

Jason M Meyer, Gregory A Graf, Deneys R van der Westhuyzen

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in lipidology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Cholesterol metabolism and tumor.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2021
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Molecular mechanisms of cellular cholesterol efflux.The Journal of biological chemistry · 2014
    Review
  14. Article
  15. Scavenger receptor class B type I and immune dysfunctions.Current opinion in endocrinology, diabetes, and obesity · 2014
    Review
  16. Article
  17. 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

3 authors at 2 institutions in 2 countries.

Jason M MeyerDepartment of Veterans Affairs Medical Center, Lexington, Kentucky, USA.
Gregory A Graf
Deneys R van der Westhuyzen
University of Kentucky · USLexington VA Health Care System · US

Funding

The role of IKKß in linking obesity to adipose tissue inflammation and adipogeneP20GM103527 · NIGMS · UNIVERSITY OF KENTUCKY · PI MORRIS, ANDREW J · 2012 to 2017
$13.7M
Mouse CoreP01HL086670 · NHLBI · UNIVERSITY OF KENTUCKY · PI DE BEER, FREDERICK C. · 2007 to 2011
$7.1M
The role of hepatic insulin resistance on SR-BI dependant HDL cholesterol uptakeR01DK100892 · NIDDK · UNIVERSITY OF KENTUCKY · PI GRAF, GREGORY A, VAN DER WESTHUYZEN, DENEYS REM · 2013 to 2016
$1.6M
Interdisciplinary Cardiovascular Training ProgramT32HL072743 · NHLBI · UNIVERSITY OF KENTUCKY · PI RANDALL, DAVID C · 2004 to 2013
$1.3M
Regulation of the ABCG5 ABCG8 Sterol TransporterR01DK080874 · NIDDK · UNIVERSITY OF KENTUCKY · PI GRAF, GREGORY A · 2009 to 2012
$1.3M
Class B Scavenger Receptors and AtherosclerosisI01BX000672 · VA · VA MEDICAL CENTER - LEXINGTON, KY · PI VAN DER WESTHUYZEN, DENEYS REM · 2009 to 2013
–
BLRD VA I01 BX000672NHLBI NIH HHS P01 HL086670NHLBI NIH HHS P01-HL-086670NHLBI NIH HHS T32 HL072743NHLBI NIH HHS T32-HL-072743NIDDK NIH HHS R01 DK080874NIDDK NIH HHS R01-DK-080874NIDDK NIH HHS R01 DK100892NIGMS NIH HHS P20 GM103527
6 · The paper itself

Abstract

purpose of reviewSelective lipid uptake (SLU) is known to be a major pathway of lipoprotein cholesterol metabolism in experimental animals and humans, but remains poorly understood. This review provides a brief overview of SLU mediated by the HDL receptor scavenger receptor B-type I (SR-BI), and highlights several surprising new findings related to the impact of SLU pathways in cholesterol homeostasis. RECENT

findingsUnder certain conditions, SR-BI-mediated SLU contributes to reverse cholesterol transport (RCT) independently of ABCG5/G8-mediated biliary cholesterol secretion, implying a novel trafficking mechanism. Hepatic SR-BI expression and RCT are decreased in diabetic mice. Farnesoid X receptor (FXR) and the microRNAs miR-185, miR-96 and miR-223 are emerging therapeutic targets for increasing SR-BI expression. SR-BI-independent selective cholesteryl ester uptake is a newly characterized pathway in macrophage foam cells. SUMMARY: New findings underscore the importance of SR-BI-mediated SLU in hepatic SLU and RCT, while indicating that further investigation is needed to define SLU pathways, including SR-BI-independent macrophage selective cholesteryl ester uptake. The intracellular trafficking of cholesterol in these pathways appears to be critical to their normal function and is a major subject of ongoing studies.

Indexed as

AnimalsATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 5Biological Transport, ActiveCholesterol EstersDiabetes MellitusHumansLipoproteinsLiverMacrophagesMiceMicroRNAsReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearScavenger Receptors, Class BABCG5 protein, humanABCG5 protein, mouseATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 5Cholesterol EstersLipoproteinsMicroRNAsReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearSCARB1 protein, humanScarb1 protein, mouseScavenger Receptors, Class B

Identifiers

PMID23842142
PMCPMC4096242
OpenAlexW2027710943

What OpenQuestion holds

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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.