Screening and Identification of Pregnancy Zone Protein and Leucine-Rich Alpha-2-Glycoprotein as Potential Serum Biomarkers for Early-Onset Myocardial Infarction using Protein Profile Analysis.


Journal

Proteomics. Clinical applications
ISSN: 1862-8354
Titre abrégé: Proteomics Clin Appl
Pays: Germany
ID NLM: 101298608

Informations de publication

Date de publication:
05 2019
Historique:
received: 02 05 2018
revised: 19 10 2018
pubmed: 10 11 2018
medline: 31 1 2020
entrez: 10 11 2018
Statut: ppublish

Résumé

The present study aims to discover novel serum biomarkers of early-onset myocardial infarction (MI) using proteomic analysis. In the first stage, the iTRAQ-coupled LC-MS/MS technique is utilized to investigate protein profiles of patients with early-onset MI. In the second stage, these candidate proteins are validated using ELISA. A total of 538 proteins are quantified, with pregnancy zone protein (PZP), leucine-rich α-2-glycoprotein (LRG) and Apolipoprotein C-I (Apo C-I) being upregulated and Apolipoprotein A-I (Apo A-I) and Apolipoprotein A-IV (Apo A-IV) downregulated in early-onset MI patients. Results from the validation stage demonstrate that the serum concentrations of PZP and LRG are significantly increased in the early-onset MI group. The correlation between the concentrations of C-reactive protein (CRP) and the two candidate biomarkers is positive. Area under the curve values used to diagnose early-onset MI for LRG and PZP are 0.939 and 0.874, respectively. Five differential serum proteins are identified in early-onset MI using proteomic analysis. Lipoprotein-related biomarkers further demonstrate the close relationship between lipid metabolism and the disease. Inflammation-associated LRG and PZP may be novel biomarkers of the disease. In addition, changes in these proteins may partly reveal the possible mechanisms in the pathogenesis and pathophysiology of early-onset MI.

Identifiants

pubmed: 30411527
doi: 10.1002/prca.201800079
doi:

Substances chimiques

Biomarkers 0
Glycoproteins 0
LRG1 protein, human 0
PZP protein, human 0
Pregnancy Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1800079

Informations de copyright

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Auteurs

Chao Xuan (C)

Department of Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, China.

Hui Li (H)

Department of Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, China.

Le-Le Li (LL)

Department of Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, China.

Qing-Wu Tian (QW)

Department of Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, China.

Qing Wang (Q)

Department of Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, China.

Bei-Bei Zhang (BB)

Department of Molecular Microbiology, Oslo University Hospital, Oslo, Norway.

Jun-Jie Guo (JJ)

Department of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, China.

Guo-Wei He (GW)

Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital,, Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Department of Surgery, Oregon Health and Science University, Portland, Oregon.

Li-Min Lun (LM)

Department of Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, China.

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Classifications MeSH