Evidence map›Paper›PMID 21628835›Full record

ReviewCirculation journal : official journal of the Japanese Circulation Society2011

Dysfunctional high-density lipoprotein and the potential of apolipoprotein A-1 mimetic peptides to normalize the composition and function of lipoproteins.

Satoshi Imaizumi, Mohamad Navab, Cecilia Morgantini, Christina Charles-Schoeman, Feng Su, Feng Gao, Murray Kwon, Ekambaram Ganapathy, David Meriwether, Robin Farias-Eisner and 2 more

Open access · bronzeAbstract readReview
In one paragraph

Review in Circulation journal : official journal of the Japanese Circulation Society, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Lipoprotein modulation of proteinuric renal injury.Laboratory investigation; a journal of technical methods and pathology · 2019
    Article
  7. Article
  8. Article
  9. Mice lackingThe Journal of biological chemistry · 2018
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  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

12 authors at 1 institution in 1 country.

Satoshi ImaizumiDepartment of Medicine, University of California, Los Angeles, CA, USA.
Mohamad Navab
Cecilia Morgantini
Christina Charles-Schoeman
Feng Su
Feng Gao
Murray Kwon
Ekambaram Ganapathy
David Meriwether
Robin Farias-Eisner
Alan M Fogelman
Srinivasa T Reddy
University of Pisa · IT

Funding

ULTRASTRUCTURE OF THE INTIMA IN EARLY LESION FORMATIONP01HL030568 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FOGELMAN, ALAN M · 1985 to 2019
$55.2M
SYNTHETIC PEPTIDE STUDIES OF THE AMPHIPATHIC HELIXP01HL034343 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SEGREST, JERE P · 1985 to 2012
$18.8M
Molecular profiling of pro-inflammatory HDLR01HL082823 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI REDDY, SRINIVASA T. · 2007 to 2011
$1.9M
HDL Function as a Biomarker for Atherosclerotic Risk in Rheumatoid ArthritisK23HL094834 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHARLES-SCHOEMAN, CHRISTINA · 2009 to 2013
$693k
NHLBI NIH HHS HL-082823NHLBI NIH HHS HL-30568NHLBI NIH HHS HL-34343NHLBI NIH HHS K23 HL094834NHLBI NIH HHS P01 HL030568NHLBI NIH HHS P01 HL034343NHLBI NIH HHS R01 HL082823
6 · The paper itself

Abstract

Although high-density lipoprotein-cholesterol (HDL-C) levels in large epidemiological studies are inversely related to the risk of coronary heart disease (CHD), increasing the level of circulating HDL-C does not necessarily decrease the risk of CHD events, CHD deaths, or mortality. HDL can act as an anti- or a pro-inflammatory molecule, depending on the context and environment. Based on a number of recent studies, it appears that the anti- or pro-inflammatory nature of HDL may be a more sensitive indicator of the presence or absence of atherosclerosis than HDL-C levels. The HDL proteome has been suggested to be a marker, and perhaps a mediator, of CHD. Apolipoprotein A-1 (apoA-I), the major protein in HDL is a selective target for oxidation by myeloperoxidase, which results in impaired HDL function. Improving HDL function through modification of its lipid and/or protein content maybe a therapeutic target for the treatment of CHD and many inflammatory disorders. HDL/apoA-I mimetic peptides may have the ability to modify the lipid and protein content of HDL and convert dysfunctional HDL to functional HDL. This review focuses on recent studies of dysfunctional HDL in animal models and human disease, and the potential of apoA-I mimetic peptides to normalize the composition and function of lipoproteins.

Indexed as

BiomimeticsAnimalsApolipoprotein A-ICoronary DiseaseDisease Models, AnimalHumansIntercellular Signaling Peptides and ProteinsLipoproteins, HDLMicePeptidesApolipoprotein A-ID-4F peptideIntercellular Signaling Peptides and ProteinsL-4F peptideLipoproteins, HDLpeptide 5FPeptides

Identifiers

PMID21628835
PMCPMC3625624
OpenAlexW1980290048

What OpenQuestion holds

Textmetadata
LicenceTDM
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.