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.
early-onset
leucine-rich alpha-2-glycoprotein
myocardial infarction
pregnancy zone protein
proteomic
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
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
e1800079Informations de copyright
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.