Evidence map›Paper›PMID 27082419›Full record

ReviewMolecular medicine reports2016

Lipid droplet-associated proteins in atherosclerosis (Review).

Janeesh Plakkal Ayyappan, Antoni Paul, Young-Hwa Goo

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular medicine reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Ginsenoside RbChinese herbal medicines · 2024
    Review
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  15. Review
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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 1 institution in 1 country.

Janeesh Plakkal AyyappanCenter for Cardovascular Sciences, Albany Medical College, Albany, NY 12208, USA.
Antoni PaulCenter for Cardovascular Sciences, Albany Medical College, Albany, NY 12208, USA.
Young-Hwa GooCenter for Cardovascular Sciences, Albany Medical College, Albany, NY 12208, USA.
Albany Medical Center Hospital · US

Funding

Targeting the Foam Cell to Prevent AtherosclerosisR01HL104251 · NHLBI · ALBANY MEDICAL COLLEGE · PI PAUL, ANTONIO · 2010 to 2014
$1.9M
American Heart Association-American Stroke Association 14SDG19690016NHLBI NIH HHS R01 HL104251
6 · The paper itself

Abstract

Accumulation of atherosclerotic plaques in arterial walls leads to major cardiovascular diseases and stroke. Macrophages/foam cells are central components of atherosclerotic plaques, which populate the arterial wall in order to remove harmful modified low‑density lipoprotein (LDL) particles, resulting in the accumulation of lipids, mostly LDL‑derived cholesterol ester, in cytosolic lipid droplets (LDs). At present, LDs are recognized as dynamic organelles that govern cellular metabolic processes. LDs consist of an inner core of neutral lipids surrounded by a monolayer of phospholipids and free cholesterol, and contain LD‑associated proteins (LDAPs) that regulate LD functions. Foam cells are characterized by an aberrant accumulation of cytosolic LDs, and are considered a hallmark of atherosclerotic lesions through all stages of development. Previous studies have investigated the mechanisms underlying foam cell formation, aiming to discover therapeutic strategies that target foam cells and intervene against atherosclerosis. It is well established that LDAPs have a major role in the pathogenesis of metabolic diseases caused by dysfunction of lipid metabolism, and several studies have linked LDAPs to the development of atherosclerosis. In this review, several foam cell‑targeting pathways have been described, with an emphasis on the role of LDAPs in cholesterol mobilization from macrophages. In addition, the potential of LDAPs as therapeutic targets to prevent the progression and/or facilitate the regression of the disease has been discussed.

Indexed as

AnimalsAtherosclerosisBiological TransportCholesterolCholesterol EstersDisease Models, AnimalFoam CellsHumansHydrolysisLipid Droplet Associated ProteinsLipid DropletsLipid MetabolismLipoproteins, LDLMacrophagesPlaque, AtheroscleroticCholesterolCholesterol EstersLipid Droplet Associated ProteinsLipoproteins, LDL

Identifiers

PMID27082419
PMCPMC4878557
OpenAlexW2330905903

What OpenQuestion holds

Textmetadata
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.