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Research ArticleExperimental Studies

Proteomic Profiling to Identify Prognostic Biomarkers in Heart Failure

PAUL A. SCOTT, BASHAR ZEIDAN, LEONG L. NG, MEHMOOD ZEB, JAMES A. ROSENGARTEN, SPIROS GARBIS, NICK P. CURZEN, JOHN M. MORGAN and PAUL A. TOWNSEND
In Vivo November 2012, 26 (6) 875-882;
PAUL A. SCOTT
1Wessex Cardiothoracic Unit, Southampton University Hospitals NHS Trust, U.K.
2Human Disease and Health, Faculty of Medicine, University of Southampton, Southampton, U.K.
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BASHAR ZEIDAN
3Cancer Sciences, Cancer Research U.K., Faculty of Medicine, University of Southampton, Southampton, U.K.
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LEONG L. NG
4Department of Cardiovascular Sciences, University Hospitals of Leicester, and NIHR Cardiovascular Biomedical Research Unit, Leicester, U.K.
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MEHMOOD ZEB
1Wessex Cardiothoracic Unit, Southampton University Hospitals NHS Trust, U.K.
2Human Disease and Health, Faculty of Medicine, University of Southampton, Southampton, U.K.
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JAMES A. ROSENGARTEN
1Wessex Cardiothoracic Unit, Southampton University Hospitals NHS Trust, U.K.
2Human Disease and Health, Faculty of Medicine, University of Southampton, Southampton, U.K.
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SPIROS GARBIS
5Department of Biotechnology, Biomedical Research Foundation of the Academy of Athens (BRFAA), Athens, Greece
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NICK P. CURZEN
1Wessex Cardiothoracic Unit, Southampton University Hospitals NHS Trust, U.K.
2Human Disease and Health, Faculty of Medicine, University of Southampton, Southampton, U.K.
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JOHN M. MORGAN
1Wessex Cardiothoracic Unit, Southampton University Hospitals NHS Trust, U.K.
2Human Disease and Health, Faculty of Medicine, University of Southampton, Southampton, U.K.
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PAUL A. TOWNSEND
3Cancer Sciences, Cancer Research U.K., Faculty of Medicine, University of Southampton, Southampton, U.K.
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  • For correspondence: p.a.townsend{at}southampton.ac.uk
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    Figure 1.

    Relationship between clinical status and biomarker peak intensity for biomarker peaks at: (A) m/z 11834, (B) m/z 14766, and (C) m/z 5351. Patients are grouped into controls, and for patients with LVEF ≤40%, by NYHA class (III/IV combined). The peak intensity levels are presented as box (25th percentile, median, 75th percentile) and whisker (10th and 90th percentiles) plots. Patient numbers are indicated. The Jonckheere-Terpstra test was used to assess the trend in peak intensity levels across patient groups.

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    Figure 2.

    Increased expression of peak m/z 11834 in patients with ICDs that died compared to those that survived. A region of mass spectra from 10 to 16 kDa has been expanded and aligned for 4 patients that died during follow-up and 4 patients that survived. Peak intensity for biomarker peak m/z 11834 (arrow) is higher in patients that died versus those that survived. The x-axis is the ratio of mass-to-charge (m/z) and the y-axis represents peak intensity.

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Vol. 26, Issue 6
November-December 2012
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Proteomic Profiling to Identify Prognostic Biomarkers in Heart Failure
PAUL A. SCOTT, BASHAR ZEIDAN, LEONG L. NG, MEHMOOD ZEB, JAMES A. ROSENGARTEN, SPIROS GARBIS, NICK P. CURZEN, JOHN M. MORGAN, PAUL A. TOWNSEND
In Vivo Nov 2012, 26 (6) 875-882;

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Proteomic Profiling to Identify Prognostic Biomarkers in Heart Failure
PAUL A. SCOTT, BASHAR ZEIDAN, LEONG L. NG, MEHMOOD ZEB, JAMES A. ROSENGARTEN, SPIROS GARBIS, NICK P. CURZEN, JOHN M. MORGAN, PAUL A. TOWNSEND
In Vivo Nov 2012, 26 (6) 875-882;
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Keywords

  • Implantable cardioverter defibrillators
  • heart failure
  • biomarkers
  • mortality
  • arrhythmias
  • proteomics
  • SELDI-TOF MS
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