Evidence map›Paper›PMID 26077962›Full record

ReviewThrombosis research2015

Understanding the role of prostaglandin E2 in regulating human platelet activity in health and disease.

Eitan A Friedman, Martin L Ogletree, Elias V Haddad, Olivier Boutaud

Open access · greenAbstract readReview
In one paragraph

Review in Thrombosis research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

21 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Frontiers in cell and developmental biology · 2023
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Effect of Prostanoids on Human Platelet Function: An Overview.International journal of molecular sciences · 2020
    Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Residual cyclooxygenase activity of aspirin-acetylated COX-2 forms 15 R-prostaglandins that inhibit platelet aggregation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    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

4 authors at 1 institution in 1 country.

Eitan A FriedmanDepartment of Medicine, Vanderbilt University, Nashville, TN 37232.
Martin L OgletreePO Box 559, Bala Cynwyd, PA 19004; Department of Pharmacology, Vanderbilt University, Nashville, TN 37232.
Elias V HaddadDepartment of Medicine, Vanderbilt University, Nashville, TN 37232.
Olivier BoutaudDepartment of Pharmacology, Vanderbilt University, Nashville, TN 37232. Electronic address: olivier.boutaud@vanderbilt.edu.
Vanderbilt University · US

Funding

THE PHARMACOLOGY OF ASPIRINP50HL081009 · NHLBI · VANDERBILT UNIVERSITY · PI LIEBLER, DANIEL · 2006 to 2010
$16.3M
Training In Cardiovascular ResearchT32HL007411 · NHLBI · VANDERBILT UNIVERSITY · PI BECKMAN, JOSHUA A · 1985 to 2020
$7.2M
NHLBI NIH HHS 5T32HL007411NHLBI NIH HHS HL081009NHLBI NIH HHS P50 HL081009NHLBI NIH HHS T32 HL007411
6 · The paper itself

Abstract

The platelet thrombus is the major pathologic entity in acute coronary syndromes, and antiplatelet agents are a mainstay of therapy. However, individual patient responsiveness to current antiplatelet drugs is variable, and all drugs carry a risk of bleeding. An understanding of the complex role of Prostaglandin E2 (PGE2) in regulating thrombosis offers opportunities for the development of novel individualized antiplatelet treatment. However, deciphering the platelet regulatory function of PGE2 has long been confounded by non-standardized experimental conditions, extrapolation of murine data to humans, and phenotypic differences in PGE2 response. This review synthesizes past and current knowledge about PGE2 effects on platelet biology, presents a rationale for standardization of experimental protocols, and provides insight into a molecular mechanism by which PGE2-activated pathways could be targeted for new personalized antiplatelet therapy to inhibit pathologic thrombosis without affecting hemostasis.

Indexed as

Models, CardiovascularPlatelet ActivationAnimalsBlood PlateletsDinoprostoneEvidence-Based MedicineHumansMiceSpecies SpecificityThrombosisDinoprostoneAntiplatelet agentEP3 antagonistplatelet aggregationplatelet inhibitorplatelet reactivity regulationprostaglandin E(2)

Identifiers

PMID26077962
PMCPMC4553088
OpenAlexW2133306113

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.