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The plasma proteomic signature as a strategic tool for early diagnosis of acute coronary syndrome.
Laborde, Carlos M; Alonso-Orgaz, Sergio; Mourino-Alvarez, Laura; Moreu, José; Vivanco, Fernando; Padial, Luis R; Barderas, María G.
Afiliação
  • Laborde CM; Laboratory of Vascular Physiopathology, Hospital Nacional de Parapléjicos, SESCAM, Toledo, Spain.
  • Alonso-Orgaz S; Laboratory of Vascular Physiopathology, Hospital Nacional de Parapléjicos, SESCAM, Toledo, Spain.
  • Mourino-Alvarez L; Laboratory of Vascular Physiopathology, Hospital Nacional de Parapléjicos, SESCAM, Toledo, Spain.
  • Moreu J; Department of Hemodynamic, Hospital Virgen de la Salud, SESCAM, Toledo, Spain.
  • Vivanco F; Department of Immunology, IIS-Fundación Jiménez Diaz, Madrid, Spain ; Department of Biochemistry and Molecular Biology I, Universidad Complutense, Madrid, Spain.
  • Padial LR; Department of Cardiology, Hospital Virgen de la Salud, Toledo, Spain.
  • Barderas MG; Laboratory of Vascular Physiopathology, Hospital Nacional de Parapléjicos, SESCAM, Toledo, Spain.
Proteome Sci ; 12: 43, 2014.
Article em En | MEDLINE | ID: mdl-26038678
ABSTRACT

BACKGROUND:

Acute coronary syndrome is the major cause of death in developed countries. Despite its high prevalence, there is still a strong need for new biomarkers which permit faster and more accurate diagnostics and new therapeutic drugs. The basis for this challenge lay in improving our understanding of the whole atherosclerotic process from atherogenesis to atherothrombosis. In this study, we conducted two different proteomic analyses of peripheral blood plasma from non-ST elevation acute coronary syndrome and ST elevation acute coronary syndrome patients vs healthy controls.

RESULTS:

Two-dimensional Fluorescence Difference in Gel Electrophoresis and mass spectrometry permitted the identification of 31 proteins with statistical differences (p < 0.05) between experimental groups. Additionally, validation by Western blot and Selected Reaction Monitoring permitted us to confirm the identification of a different and characteristic plasma proteomic signature for NSTEACS and STEACS patients.

CONCLUSIONS:

We purpose the severity of hypoxia as the cornerstone for explaining the differences observed between both groups.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Idioma: En Ano de publicação: 2014 Tipo de documento: Article