Evidence map›Paper›PMID 11238037›Full record

ArticleThe American journal of pathology2001

Macrophage myeloperoxidase regulation by granulocyte macrophage colony-stimulating factor in human atherosclerosis and implications in acute coronary syndromes.

S Sugiyama, Y Okada, G K Sukhova, R Virmani, J W Heinecke, P Libby

Open access · greenAbstract read
In one paragraph

Article in The American journal of pathology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 202 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
202citing papers in PubMed, 1 pooled it
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.

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

202 citing papers in PubMed, 1 synthesis or guideline pooled it, 698 citations in OpenAlex.

  1. Pooled it
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  6. Article
  7. Myeloperoxidase as a therapeutic target for oxidative damage in Alzheimer's disease.Journal of enzyme inhibition and medicinal chemistry · 2025
    Review
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142 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 1 country.

S SugiyamaDepartment of Medicine, Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, 221 Longwood Ave., Boston, MA 02115, USA.
Y Okada
G K Sukhova
R Virmani
J W Heinecke
P Libby
Harvard University · USArmed Forces Institute of Pathology · USBrigham and Women's Hospital · USWashington University in St. Louis · US

Funding

Inflammatory Mechanisms of AtherosclerosisR01HL034636 · NHLBI · TUFTS UNIVERSITY BOSTON · PI LIBBY, PETER · 1985 to 2006
$1.9M
CONTROL OF GROWTH OF VASCULAR WALL CELLSR37HL034636 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LIBBY, PETER · 1993 to 2002
$1.2M
REACTIVE ALDEHYDES AND CARDIOVASCULAR AGINGR01AG015013 · NIA · WASHINGTON UNIVERSITY · PI HEINECKE, JAY W · 1998 to 2002
$799k
MYELOPEROXIDASE-MEDIATED VASCULAR INJURYR01AG012293 · NIA · WASHINGTON UNIVERSITY · PI HEINECKE, JAY W · 1995 to 1999
–
NHLBI NIH HHS HL34636NHLBI NIH HHS R01 HL034636NHLBI NIH HHS R37 HL034636NIA NIH HHS AG12293NIA NIH HHS AG15013
6 · The paper itself

Abstract

Inflammation and oxidative stress contribute to the pathogenesis of many human diseases including atherosclerosis. Advanced human atheroma contains high levels of the enzyme myeloperoxidase that produces the pro-oxidant species, hypochlorous acid (HOCl). This study documents increased numbers of myeloperoxidase-expressing macrophages in eroded or ruptured plaques causing acute coronary syndromes. In contrast, macrophages in human fatty streaks contain little or no myeloperoxidase. Granulocyte macrophage colony-stimulating factor, but not macrophage colony-stimulating factor, selectively regulates the ability of macrophages to express myeloperoxidase and produce HOCl in vitro. Moreover, myeloperoxidase-positive macrophages in plaques co-localized with granulocyte macrophage colony-stimulating factor. Pro-inflammatory stimuli known to be present in human atherosclerotic plaque, including CD40 ligand, lysophosphatidylcholine, or cholesterol crystals, could induce release of myeloperoxidase from HOCl production by macrophages in vitro. HOCl-modified proteins accumulated at ruptured or eroded sites of human coronary atheroma. These results identify granulocyte macrophage colony-stimulating factor as an endogenous regulator of macrophage myeloperoxidase expression in human atherosclerosis and support a particular role for the myeloperoxidase-expressing macrophages in atheroma complication and the acute coronary syndromes.

Indexed as

ArteriosclerosisCD40 AntigensCell DifferentiationCells, CulturedCholesterolGene Expression RegulationGranulocyte-Macrophage Colony-Stimulating FactorHumansHypochlorous AcidLysophosphatidylcholinesMacrophagesMonocytesMyocardial InfarctionPeroxidasePhenotypeReactive Oxygen SpeciesCD40 AntigensCholesterolGranulocyte-Macrophage Colony-Stimulating FactorHypochlorous AcidLysophosphatidylcholinesPeroxidaseReactive Oxygen Species

Identifiers

PMID11238037
PMCPMC1850342
OpenAlexW1964457547

What OpenQuestion holds

Textmetadata
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.