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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

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Autor(es):
Flores-Nascimento, Mariane C. [1] ; Paes-Leme, Adriana F. [2] ; Mazetto, Bruna M. [1] ; Zanella, Jaqueline L. [2] ; De Paula, Erich V. [1] ; Annichino-Bizzacchi, Joyce M. [1]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] State Univ Campinas UNICAMP, Hematol & Hemotherapy Ctr, BR-13083970 Campinas, SP - Brazil
[2] Biosci Natl Lab LNBio, Campinas, SP - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: THROMBOSIS RESEARCH; v. 130, n. 5, p. E246-E250, NOV 2012.
Citações Web of Science: 2
Resumo

Introduction: Deep vein thrombosis (DVT) is a multi-causal disease associated with high morbidity and mortality due to complications, and 25% of patients present recurrence within 5 years. The identification of factors involved with DVT can help in the management of patients, prevention of recurrence and in the development of new therapies. The evaluation of plasma components using proteomics potentially provides a window into the individual's state of health. We analyzed the protein profile of plasma samples from 3 DVT patients and compared results to those obtained from 1 sibling and 1 neighbor of each patient. These patients were selected as they presented a personal and family history of spontaneous and recurrent episodes of proximal DVT. Material And Methods: Albumin was removed using Affi-Gel Blue Gel, and the proteins were alkylated, reduced, precipitated and hydrolyzed. The peptides were fractionated by SCX chromatography, the 7 fractions obtained were directed to the ESI Q-TOF Premier mass spectrometer. Protein search was performed using the Mascot engine against the IPI human database. Results: Proteins that were statistically overexpressed in DVT patients included C4-A plasma protease, C1 inter-alpha-trypsin inhibitor, heavy chain H inhibitor and serum amyloid A. Proteins that were statistically reduced in DVT patients included alpha-2-HS- glycoprotein, isoform 2 of inter-alpha-trypsin inhibitor heavy chain H4 and apolipoprotein A-IV. Conclusions: The evaluation of plasma from patients with spontaneous DVT allows the identification of differently expressed proteins when compared to controls; this expression may be of pathological importance for immune and inflammatory processes in DVT. (c) 2012 Elsevier Ltd. All rights reserved. (AU)