Evidence map›Paper›PMID 22017929›Full record

ReviewJACC. Cardiovascular interventions2011

Vascular inflammation and repair: implications for re-endothelialization, restenosis, and stent thrombosis.

Teruo Inoue, Kevin Croce, Toshifumi Morooka, Masashi Sakuma, Koichi Node, Daniel I Simon

2 registry-linked trialsOpen access · greenAbstract readReview
In one paragraph

Review in JACC. Cardiovascular interventions, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 208 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
208citing papers in PubMed, 5 pooled it
26.5field-weighted citation impact, top 1% 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
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

208 citing papers in PubMed, 5 syntheses or guidelines pooled it, 467 citations in OpenAlex.

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  4. Abbreviated versus Standard Duration of DAPT after PCI: A Systematic Review and Network Meta-analysis.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2022
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148 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

6 authors at 4 institutions in 2 countries.

Teruo InoueDepartment of Cardiovascular Medicine, Dokkyo Medical University, Tochigi, Japan.
Kevin Croce
Toshifumi Morooka
Masashi Sakuma
Koichi Node
Daniel I Simon
Saga University · JPUniversity Hospitals of Cleveland · USBrigham and Women's Hospital · USDokkyo Medical University · JP

Funding

Inflammation in Vascular Injury and RepairR37HL057506 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI SIMON, DANIEL I · 2007 to 2016
$4.1M
Inflammation in Vascular Injury and RepairR01HL057506 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI SIMON, DANIEL I · 1997 to 2006
$2.4M
Monocyte Differentiation and Mac-1-Regulated ForkheadR01HL073852 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI SIMON, DANIEL I · 2003 to 2006
$1.6M
MRP-14 and Cardiovascular DiseaseR01HL085816 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI SIMON, DANIEL I · 2007 to 2010
$1.6M
MRP-14, Platelets and AtherothrombosisK08HL086672 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI CROCE, KEVIN J · 2008 to 2012
$682k
NHLBI NIH HHS 1K08HL086672NHLBI NIH HHS HL57506NHLBI NIH HHS HL73852NHLBI NIH HHS HL85816NHLBI NIH HHS K08 HL086672NHLBI NIH HHS R01 HL057506NHLBI NIH HHS R01 HL073852NHLBI NIH HHS R01 HL085816NHLBI NIH HHS R37 HL057506
6 · The paper itself

Abstract

The cellular and molecular processes that control vascular injury responses after percutaneous coronary intervention involve a complex interplay among vascular cells and progenitor cells that control arterial remodeling, neointimal proliferation, and re-endothelialization. Drug-eluting stents (DES) improve the efficacy of percutaneous coronary intervention by modulating vascular inflammation and preventing neointimal proliferation and restenosis. Although positive effects of DES reduce inflammation and restenosis, negative effects delay re-endothelialization and impair endothelial function. Delayed re-endothelialization and impaired endothelial function are linked to stent thrombosis and adverse clinical outcomes after DES use. Compared with bare-metal stents, DES also differentially modulate mobilization, homing, and differentiation of vascular progenitor cells involved in re-endothelialization and neointimal proliferation. The effects of DES on vascular inflammation and repair directly impact clinical outcomes with these devices and dictate requirements for extended-duration dual antiplatelet therapy.

Indexed as

Drug-Eluting StentsAngioplasty, Balloon, CoronaryAntigens, CD34Cardiovascular DiseasesCoronary RestenosisCoronary ThrombosisEndothelium, VascularHumansInflammationLeukocytesRisk FactorsSirolimusAntigens, CD34Sirolimus

Identifiers

PMID22017929
PMCPMC3341937
OpenAlexW13897408

What OpenQuestion holds

Textmetadata
LicenceTDM
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.