Evidence map›Paper›PMID 12860861›Full record

Trial reportHeart (British Cardiac Society)2003

Increased urinary 15-F2t-isoprostane concentrations in patients with non-ischaemic congestive heart failure: a marker of oxidative stress.

M Nonaka-Sarukawa, K Yamamoto, H Aoki, H Takano, T Katsuki, U Ikeda, K Shimada

2 registry-linked trialsOpen access · bronzeAbstract readClinical TrialControlled Clinical Trial
In one paragraph

Trial report in Heart (British Cardiac Society), 2003. 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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 9% 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.

NCT01052272 phase2 / phase3completednot on this mapstarted 2005, after this paper: background citation

Phase 2/3 Study of Effect of AT1RB Versus ACE Inhibitor in Addition to XO Inhibitor on Progression of LV Remodeling and Dysfunction in Diabetic Patients With Acute MI.

TypeinterventionalSponsorUniversity of Alabama at BirminghamRan2005 to 2010Enrolled72ConditionsDiabetesArmsRamipril, Candesartan cilexetil, Allopurinol
NCT01052428 phase2 / phase3completednot on this mapstarted 2004, after this paper: background citation

Molecular Mechanisms of Volume Overload-Aim 1(SCCOR in Cardiac Dysfunction and Disease)

TypeinterventionalSponsorUniversity of Alabama at BirminghamRan2004 to 2010Enrolled38ConditionsMitral RegurgitationArmsmetoprolol succinate (Toprol XL), Placebo
3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
  2. Article
  3. Effects of Coenzyme QAntioxidants (Basel, Switzerland) · 2022
    Article
  4. A review of the "OMICS" for management of patients with obstructive sleep apnoea.Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale · 2020
    Review
  5. Article
  6. Review
  7. Article
  8. Cardiac biomarkers in children with congenital heart disease.World journal of pediatrics : WJP · 2015
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Role of xanthine oxidoreductase in cardiac nitroso-redox imbalance.Frontiers in bioscience (Landmark edition) · 2009
    Review
  14. Article
  15. Article
  16. Review
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

M Nonaka-SarukawaDivision of Cardiovascular Medicine, Jichi Medical School, Minamikawachi-Machi, Tochigi 329-0498, Japan.
K Yamamoto
H Aoki
H Takano
T Katsuki
U Ikeda
K Shimada
Jichi Medical University · JPKawagoe Technical High School · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate a novel marker of oxidative stress in patients with congestive heart failure (CHF). PATIENTS: 15 patients with mild CHF, 15 patients with severe CHF with acute exacerbation, and 15 control subjects.

main outcome measuresMeasurement of urinary 15-F2t-isoprostane, plasma brain natriuretic peptide (BNP), serum interleukin 6 (IL-6), and serum thrombomodulin concentrations. In patients with severe CHF, samples were taken at admission and 4, 7, and 14 days after admission.

resultsUrinary 15-F2t-isoprostane, plasma BNP, and serum IL-6 concentrations in patients with severe CHF were significantly higher than those in control subjects or in patients with mild CHF. However, concentrations of serum thrombomodulin, a marker of endothelial damage, were not different between patients with CHF and control subjects. In addition, urinary 15-F2t-isoprostane, plasma BNP, and serum IL-6 concentrations in patients with severe CHF gradually decreased in proportion to the severity of CHF during hospitalisation. Interestingly, urinary 15-F2t-isoprostane concentrations significantly correlated with plasma BNP concentrations and serum IL-6 concentrations, but not with serum thrombomodulin concentrations.

conclusionsUrinary 15-F2t-isoprostane concentrations increased in proportion to the severity of CHF in patients. This may be caused by increased 15-F2t-isoprostane production. These findings suggest that urinary 15-F2t-isoprostane may be a marker of morbidity as well as oxidative stress in patients with CHF.

Indexed as

AgedAged, 80 and overBiomarkersF2-IsoprostanesFemaleHeart FailureHumansInterleukin-6MaleMiddle AgedNatriuretic Peptide, BrainOxidative StressThrombomodulinBiomarkersF2-IsoprostanesInterleukin-6Natriuretic Peptide, BrainThrombomodulin

Identifiers

PMID12860861
PMCPMC1767773
OpenAlexW2169155656

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.