Evidence map›Paper›PMID 33327749›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2021

Lysolipids in Vascular Development, Biology, and Disease.

Eric Engelbrecht, Calum A MacRae, Timothy Hla

Open access · greenAbstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2021. 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
1.7field-weighted citation impact, top 15% 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, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Observational
  8. Article
  9. Article
  10. Article
  11. Article
  12. Calpain and Cardiometabolic Diseases.International journal of molecular sciences · 2023
    Review
  13. Article
  14. The Vasculature in Pulmonary Fibrosis.Current tissue microenvironment reports · 2022
    Article
  15. Article
  16. Review
  17. Lysophospholipid Mediators in Health and Disease.Annual review of pathology · 2022
    Review
  18. Article
  19. Sphingosine 1-Phosphate Metabolism and Signaling.Advances in experimental medicine and biology · 2022
    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

3 authors at 2 institutions in 1 country.

Eric EngelbrechtVascular Biology Program, Boston Children's Hospital, Department of Surgery (E.E., T.H.), Harvard Medical School, Boston, MA.
Calum A MacRaeDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Department of Medicine (C.A.M.), Harvard Medical School, Boston, MA.
Timothy HlaVascular Biology Program, Boston Children's Hospital, Department of Surgery (E.E., T.H.), Harvard Medical School, Boston, MA.
Boston Children's Hospital · USBrigham and Women's Hospital · US

Funding

Mechanisms of sphingolipid signaling in vascular health and diseaseR35HL135821 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI HLA, TIMOTHY TUN · 2017 to 2023
$6.3M
Sphingolipid signaling in age-associated vascular pathologyR56AG069825 · NIA · BOSTON CHILDREN'S HOSPITAL · PI HLA, TIMOTHY TUN · 2020 to 2020
$363k
NHLBI NIH HHS R35 HL135821NIA NIH HHS R56 AG069825
6 · The paper itself

Abstract

Membrane phospholipid metabolism forms lysophospholipids, which possess unique biochemical and biophysical properties that influence membrane structure and dynamics. However, lysophospholipids also function as ligands for G-protein-coupled receptors that influence embryonic development, postnatal physiology, and disease. The 2 most well-studied species-lysophosphatidic acid and S1P (sphingosine 1-phosphate)-are particularly relevant to vascular development, physiology, and cardiovascular diseases. This review summarizes the role of lysophosphatidic acid and S1P in vascular developmental processes, endothelial cell biology, and their roles in cardiovascular disease processes. In addition, we also point out the apparent connections between lysophospholipid biology and the Wnt (int/wingless family) pathway, an evolutionarily conserved fundamental developmental signaling system. The discovery that components of the lysophospholipid signaling system are key genetic determinants of cardiovascular disease has warranted current and future research in this field. As pharmacological approaches to modulate lysophospholipid signaling have entered the clinical sphere, new findings in this field promise to influence novel therapeutic strategies in cardiovascular diseases.

Indexed as

AnimalsCardiovascular DiseasesCardiovascular SystemEndothelial CellsHumansLigandsLysophospholipidsMorphogenesisReceptors, Lysophosphatidic AcidReceptors, LysophospholipidSphingosineSphingosine-1-Phosphate ReceptorsWnt Signaling PathwayLigandslysophosphatidic acidLysophospholipidsReceptors, Lysophosphatidic AcidReceptors, LysophospholipidSphingosinesphingosine 1-phosphateSphingosine-1-Phosphate Receptorscardiovascular diseasesembryonic developmentendothelial cellslysophospholipidssphingosine

Identifiers

PMID33327749
PMCPMC8105276
OpenAlexW3112931142

What Socratic 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 Socratic graph.