Evidence map›Paper›PMID 15166790›Full record

ReviewCurrent opinion in lipidology2004

Electronegative low-density lipoprotein.

José Luis Sánchez-Quesada, Sonia Benítez, Jordi Ordóñez-Llanos

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Current opinion in lipidology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00988364 (Effects of Ezetimibe, Simvastatin, and Vytorin on Reducing L5 in Patients With Metabolic Syndrome), which is not on this map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.5field-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.

NCT00988364 phase4completedstarted 2007, after this paper: background citation

Effects of Ezetimibe, Simvastatin, and Vytorin on Reducing L5 in Patients With Metabolic Syndrome

Ran2007Enrolled30Registered outcomes2Posted comparisons0ConditionsMetabolic SyndromeArmsEzetimibe, Placebo, simvastatin, Vytorin
Open the trial in the graph
3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 138 citations in OpenAlex.

  1. Trial
  2. Review
  3. Atherogenic circulating lipoproteins in ischemic stroke.Frontiers in cardiovascular medicine · 2024
    Review
  4. Article
  5. Can Electronegative LDL Act as a Multienzymatic Complex?International journal of molecular sciences · 2023
    Review
  6. Review
  7. Presence of Ceramidase Activity in Electronegative LDL.International journal of molecular sciences · 2022
    Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

3 authors at 2 institutions in 2 countries.

José Luis Sánchez-QuesadaBiochemistry Department and Research Institute, Hospital de la Santa Creu i Sant Pau, C/Antoni Maria Claret 167, 08025 Barcelona, Spain.
Sonia Benítez
Jordi Ordóñez-Llanos
Hospital de Sant Pau · ESUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewThe occurrence in blood of an electronegatively charged LDL was described in 1988. During the 1990s reports studying electronegative LDL (LDL(-)) were scant and its atherogenic role controversial. Nevertheless, recent reports have provided new evidence on a putative atherogenic role of LDL(-). This review focuses on and discusses these new findings. RECENT

findingsIn recent years, LDL(-) has been found to be involved in several atherogenic features through its action on cultured endothelial cells. LDL(-) induces the production of chemokines, such as IL-8 and monocyte chemotactic protein 1, and increases tumor necrosis factor-alpha-induced production of vascular cell adhesion molecule 1, with these molecules being involved in early phases of leukocyte recruitment. LDL(-) from familial hypercholesterolemic patients also decreases DNA synthesis and intracellular fibroblast growth factor 2 production, which may contribute to impaired angiogenesis and increased apoptosis. In addition, the preferential association of platelet-activating factor acetylhydrolase with LDL(-) has been reported, suggesting a proinflammatory role of this enzyme in LDL(-). SUMMARY: Recent findings suggest that LDL(-) could contribute to atherogenesis via several mechanisms, including proinflammatory, proapoptotic and anti-angiogenesis properties. Further studies are required to define the role of LDL(-) in atherogenesis more precisely and to clarify mechanisms involved in endothelial cell activation.

Indexed as

AnimalsArteriosclerosisCardiovascular DiseasesElectricityEndothelium, VascularFibroblast Growth Factor 2HumansInflammationInterleukin-8Lipoproteins, LDLRiskTumor Necrosis Factor-alphaVascular Cell Adhesion Molecule-1Fibroblast Growth Factor 2Interleukin-8Lipoproteins, LDLTumor Necrosis Factor-alphaVascular Cell Adhesion Molecule-1

Identifiers

PMID15166790
OpenAlexW2416189419

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.