Evidence map›Paper›PMID 21126576›Full record

ReviewFree radical biology & medicine2011

F2-isoprostanes as an indicator and risk factor for coronary heart disease.

Sean S Davies, L Jackson Roberts

Abstract readReview
In one paragraph

Review in Free radical biology & medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 3% 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

65 citing papers in PubMed, 1 synthesis or guideline pooled it, 153 citations in OpenAlex.

  1. Pooled it
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  8. Implications ofAntioxidants (Basel, Switzerland) · 2025
    Article
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5 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

2 authors at 1 institution in 1 country.

Sean S DaviesDivision of Clinical Pharmacology and Department of Pharmacology, Vanderbilt University, Nashville, TN 37221, USA. sean.davies@vanderbilt.edu
L Jackson Roberts
Vanderbilt University · US

Funding

THE PHARMACOLOGY OF INHIBITORS OF HEME PROTEIN-CATALYZED LIPID PEROXIDATIONP50GM015431 · NIGMS · VANDERBILT UNIVERSITY · PI CAPRIOLI, RICHARD M · 1985 to 2010
$15.0M
Therapeutic Modulation of Endothelial Cell TetrahydrobiopterinP01GM015431 · NIGMS · VANDERBILT UNIVERSITY · PI ROBERTS, II, L JACKSON · 2011 to 2015
$9.5M
Structural Identification of Prostaglandin ConjugatesR37GM042056 · NIGMS · VANDERBILT UNIVERSITY · PI ROBERTS, II, L JACKSON · 2001 to 2010
$6.5M
Transformed Probiotic Bacteria for Treatment of Chronic DiseasesDP2OD003137 · OD · VANDERBILT UNIVERSITY · PI DAVIES, SEAN STEPHEN · 2007 to 2007
$2.3M
Oxidative Stress Na Channel Gating and ArrhythmiasR01HL079365 · NHLBI · VANDERBILT UNIVERSITY · PI ROBERTS, L JACKSON · 2005 to 2007
$932k
STRUCTURAL IDENTIFICATION OF PROSTAGLANDIN CONJUGATESR01GM042056 · NIGMS · VANDERBILT UNIVERSITY · PI ROBERTS, L JACKSON · 1989 to 2000
$441k
NHLBI NIH HHS HL079365NHLBI NIH HHS R01 HL079365NIGMS NIH HHS GM15431NIGMS NIH HHS GM42056NIGMS NIH HHS P01 GM015431NIGMS NIH HHS P50 GM015431NIGMS NIH HHS R01 GM042056NIGMS NIH HHS R37 GM042056NIH HHS DP2 OD003137NIH HHS OD003137
6 · The paper itself

Abstract

Coronary heart disease (CHD) is the leading single cause of death in the United States and most Western countries, killing more than 400,000 Americans per year. Although CHD often manifests suddenly as a fatal myocardial infarction, the atherosclerosis that gives rise to the infarction develops gradually and can be markedly slowed or even reversed through pharmacological and lifestyle interventions. These same atherosclerotic processes also drive related vascular diseases such as stroke and peripheral artery disease, and individuals surviving occlusive events often develop additional complications including ischemic cardiomyopathy and heart failure. Therefore, better detection of subclinical atherosclerosis, along with more effective treatments, could significantly reduce the rate of death from CHD and related vascular diseases in the United States. In recent years, oxidation of polyunsaturated fatty acids (PUFAs) in plasma lipoproteins has been postulated to be a critical step in the development of atherosclerosis. If so, then monitoring lipid peroxidation should be a useful indicator of disease risk and progression. This review focuses on the evidence that specific PUFA peroxidation products, the F(2)-isoprostanes, are useful biomarkers that could potentially be utilized as indicators of CHD.

Indexed as

Lipid PeroxidationAtherosclerosisBiomarkersCoronary DiseaseF2-IsoprostanesHumansLipoproteinsRisk FactorsBiomarkersF2-IsoprostanesLipoproteins

Identifiers

PMID21126576
PMCPMC3058898
OpenAlexW1991291137

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.