Evidence map›Paper›PMID 20709806›Full record

ArticleThe American journal of pathology2010

Aspirin-triggered lipoxin and resolvin E1 modulate vascular smooth muscle phenotype and correlate with peripheral atherosclerosis.

Karen J Ho, Matthew Spite, Christopher D Owens, Hope Lancero, Alex H K Kroemer, Reena Pande, Mark A Creager, Charles N Serhan, Michael S Conte

3 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 126 papers.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed
8.4field-weighted citation impact, top 2% 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.

NCT02719665 nacompletednot on this mapstarted 2016, after this paper: background citation

THE OMEGA-SPM-DOSE and OMEGA-SPM-PAD: Specialized Pro-Resolving Mediators in Patients With Peripheral Artery Disease

TypeinterventionalSponsorUniversity of California, San FranciscoRan2016 to 2020Enrolled30ConditionsPeripheral Arterial Disease, Claudication, Claudication, Intermittent, Vascular OcclusionArmsSPM Emulsion, Dose-modality, SPM Softgel, Dose-Modality, Placebo Softgel
NCT03208920 nacompletednot on this mapstarted 2016, after this paper: background citation

Omega EVAR: Use of Fish Oil to Reduce Inflammation During Endovascular Abdominal Aortic Repair.

TypeinterventionalSponsorUniversity of California, San FranciscoRan2016 to 2018Enrolled2ConditionsPAD, Abdominal Aortic AneurysmArmsPro-Omega, ProOmega Placebo
NCT03590769 phase1completednot on this mapstarted 2017, after this paper: background citation

Arterial Imaging of Inflammation and Resolution After Endovascular Surgery

TypeinterventionalSponsorUniversity of California, San FranciscoRan2017 to 2019Enrolled9ConditionsPeripheral Arterial Disease, Claudication, Intermittent, Claudication, PADArms18F-FDG
3 · Its place in the literature

Who cites it

126 citing papers in PubMed, 200 citations in OpenAlex.

  1. Trial
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  4. Specialized proresolving lipid mediators in patients with coronary artery disease and their potential for clot remodeling.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
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  8. Article
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  10. Impacts of Oxylipins on ischemic stroke: from pathophysiology to clinical phenotypes.Metabolomics : Official journal of the Metabolomic Society · 2025
    Review
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  14. Article
  15. Article
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  18. Omega-3 (Nutrients · 2024
    Review
  19. Review
  20. Cryo-EM structure of the human chemerin receptor 1-Gi protein complex bound to the C-terminal nonapeptide of chemerin.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article

66 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 1 country.

Karen J HoDivision of Vascular and Endovascular Surgery, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Matthew Spite
Christopher D Owens
Hope Lancero
Alex H K Kroemer
Reena Pande
Mark A Creager
Charles N Serhan
Michael S Conte
Brigham and Women's Hospital · USBeth Israel Deaconess Medical Center · USUniversity of California, San Francisco · US

Funding

Specialized Center for Oral Inflammation and ResolutionP50DE016191 · NIDCR · BRIGHAM AND WOMEN'S HOSPITAL · PI SERHAN, CHARLES NICHOLAS · 2004 to 2010
$13.6M
STEM CELLS AND DIABETIC CARDIOMYOPATHY PROJ 2 2009P20RR024489 · NCRR · UNIVERSITY OF LOUISVILLE · PI ROKOSH, GREGG · 2008 to 2011
$10.0M
Inflammation and Insulin Resistance in PADR01HL075771 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI CREAGER, MARK A · 2003 to 2007
$4.5M
Endothelial Function and Peripheral Vein Bypass Graft RemodelingK23HL092163 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI OWENS, CHRISTOPHER DEAN · 2008 to 2012
$635k
The role of anti-inflammatory lipid mediators in atherogenesisF32HL087526 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SPITE, MATTHEW R · 2008 to 2009
$76k
NCRR NIH HHS P20 RR024489NCRR NIH HHS P20-RR024489NHLBI NIH HHS F32 HL087526NHLBI NIH HHS HL087526NHLBI NIH HHS HL75771NHLBI NIH HHS K23 HL092163NHLBI NIH HHS K23 HL-92163NHLBI NIH HHS R01 HL075771NIDCR NIH HHS P50 DE016191NIDCR NIH HHS P50-DE016191
6 · The paper itself

Abstract

Atherosclerosis is a chronic inflammatory disease of the vessel wall. Recent evidence suggests that chronic vascular inflammation ensues as an imbalance between pro- and anti-inflammatory mediators. Recently identified lipid mediators (eg, lipoxins and resolvins) play active roles in promoting the resolution of inflammation. Alterations in vascular smooth muscle cell (VSMC) phenotype, which manifest as a loss of contractile protein expression and increased proliferation and migration, are prominent mechanistic features of both atherosclerosis and restenosis following various interventions (eg, angioplasty and bypass grafting). We sought to determine whether human atherosclerosis is associated with a "resolution deficit" and whether lipoxins and resolvins influence VSMC phenotype. Here we report that plasma levels of aspirin-triggered lipoxin are significantly lower in patients with symptomatic peripheral artery disease than in healthy volunteers. Both aspirin-triggered lipoxin and resolvin E1 block platelet-derived growth factor-stimulated migration of human saphenous vein SMCs and decrease phosphorylation of the platelet-derived growth factor receptor-β. Importantly, receptors for aspirin-triggered lipoxin and resolvin E1 (ALX and ChemR23, respectively) were identified in human VSMCs. Overall, these results demonstrate that stimulatory lipid mediators confer a protective phenotypic switch in VSMCs and elucidate new functions for these mediators in the regulation of SMC biology. These results also suggest that peripheral artery disease is associated with an inflammation-resolution deficit and highlight a potential therapeutic opportunity for the regulation of vascular injury responses.

Indexed as

Adaptor Proteins, Signal TransducingAgedAnti-Inflammatory AgentsAspirinAtherosclerosisBlotting, WesternCase-Control StudiesCell SurvivalChemotaxisEicosapentaenoic AcidFemaleFlow CytometryHumansImmunoenzyme TechniquesLipoxinsMale5S,12R,18R-trihydroxy-6Z,8E,10E,14Z,16E-eicosapentaenoic acidAdaptor Proteins, Signal TransducingAnti-Inflammatory AgentsAspirinCMKLR1 protein, humanEicosapentaenoic AcidHSH2D protein, humanLipoxinsPlatelet-Derived Growth FactorReceptors, ChemokineReceptors, Platelet-Derived Growth FactorRNA, Messenger

Identifiers

PMID20709806
PMCPMC2947304
OpenAlexW2003076495

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.