Cargando…
Serum prolidase activity in patients with cardiac syndrome X
OBJECTIVE: Although the underlying mechanism is not yet fully understood, Cardiac Syndrome X (CSX) is defined as microvascular dysfunction. Prolidase plays a role in collagen synthesis. Increased serum prolidase activity (SPA) has been shown to correlate with collagen turnover. Augmented collagen tu...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kare Publishing
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603856/ https://www.ncbi.nlm.nih.gov/pubmed/33163883 http://dx.doi.org/10.14744/nci.2020.09086 |
_version_ | 1783604014803320832 |
---|---|
author | Aciksari, Gonul Demir, Bulent Uygun, Turgut Gedikbasi, Asuman Kutlu, Orkide Atici, Adem Baycan, Omer Faruk Kocak, Mehmet Kul, Seref |
author_facet | Aciksari, Gonul Demir, Bulent Uygun, Turgut Gedikbasi, Asuman Kutlu, Orkide Atici, Adem Baycan, Omer Faruk Kocak, Mehmet Kul, Seref |
author_sort | Aciksari, Gonul |
collection | PubMed |
description | OBJECTIVE: Although the underlying mechanism is not yet fully understood, Cardiac Syndrome X (CSX) is defined as microvascular dysfunction. Prolidase plays a role in collagen synthesis. Increased serum prolidase activity (SPA) has been shown to correlate with collagen turnover. Augmented collagen turn-over may be associated with vascular fibrosis and microvascular dysfunction. In this study, we assessed whether there was a correlation between CXS and prolidase activity. METHODS: This case-control study included 45 consecutive CSX patients (mean age 50.7±6.5 years, 27 women) and 40 healthy controls (mean age 51.2±6.5 years, 25 women). Prolidase activity was determined with the Human Xaa-Pro Dipeptidase/Prolidase enzyme-linked immunosorbent assay kit (Cusabio Biotech Co. Ltd, China). RESULTS: Mean prolidase activity was 898.8±639.1 mU/mL in the CSX group and 434.1±289.8 mU/mL in the control group (p<0.001). In ROC analysis, it was found that the SPA value above 350 mU/mL sympathizes with the diagnosis of CSX. CONCLUSION: Increased SPA in CXS patients may play an essential role in the pathophysiology of CSX, leading to augmented oxidative stress and vascular fibrosis, endothelial dysfunction, and increased microvascular resistance. |
format | Online Article Text |
id | pubmed-7603856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Kare Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-76038562020-11-06 Serum prolidase activity in patients with cardiac syndrome X Aciksari, Gonul Demir, Bulent Uygun, Turgut Gedikbasi, Asuman Kutlu, Orkide Atici, Adem Baycan, Omer Faruk Kocak, Mehmet Kul, Seref North Clin Istanb Original Article OBJECTIVE: Although the underlying mechanism is not yet fully understood, Cardiac Syndrome X (CSX) is defined as microvascular dysfunction. Prolidase plays a role in collagen synthesis. Increased serum prolidase activity (SPA) has been shown to correlate with collagen turnover. Augmented collagen turn-over may be associated with vascular fibrosis and microvascular dysfunction. In this study, we assessed whether there was a correlation between CXS and prolidase activity. METHODS: This case-control study included 45 consecutive CSX patients (mean age 50.7±6.5 years, 27 women) and 40 healthy controls (mean age 51.2±6.5 years, 25 women). Prolidase activity was determined with the Human Xaa-Pro Dipeptidase/Prolidase enzyme-linked immunosorbent assay kit (Cusabio Biotech Co. Ltd, China). RESULTS: Mean prolidase activity was 898.8±639.1 mU/mL in the CSX group and 434.1±289.8 mU/mL in the control group (p<0.001). In ROC analysis, it was found that the SPA value above 350 mU/mL sympathizes with the diagnosis of CSX. CONCLUSION: Increased SPA in CXS patients may play an essential role in the pathophysiology of CSX, leading to augmented oxidative stress and vascular fibrosis, endothelial dysfunction, and increased microvascular resistance. Kare Publishing 2020-08-17 /pmc/articles/PMC7603856/ /pubmed/33163883 http://dx.doi.org/10.14744/nci.2020.09086 Text en Copyright: © 2020 by Istanbul Northern Anatolian Association of Public Hospitals http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License |
spellingShingle | Original Article Aciksari, Gonul Demir, Bulent Uygun, Turgut Gedikbasi, Asuman Kutlu, Orkide Atici, Adem Baycan, Omer Faruk Kocak, Mehmet Kul, Seref Serum prolidase activity in patients with cardiac syndrome X |
title | Serum prolidase activity in patients with cardiac syndrome X |
title_full | Serum prolidase activity in patients with cardiac syndrome X |
title_fullStr | Serum prolidase activity in patients with cardiac syndrome X |
title_full_unstemmed | Serum prolidase activity in patients with cardiac syndrome X |
title_short | Serum prolidase activity in patients with cardiac syndrome X |
title_sort | serum prolidase activity in patients with cardiac syndrome x |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603856/ https://www.ncbi.nlm.nih.gov/pubmed/33163883 http://dx.doi.org/10.14744/nci.2020.09086 |
work_keys_str_mv | AT aciksarigonul serumprolidaseactivityinpatientswithcardiacsyndromex AT demirbulent serumprolidaseactivityinpatientswithcardiacsyndromex AT uygunturgut serumprolidaseactivityinpatientswithcardiacsyndromex AT gedikbasiasuman serumprolidaseactivityinpatientswithcardiacsyndromex AT kutluorkide serumprolidaseactivityinpatientswithcardiacsyndromex AT aticiadem serumprolidaseactivityinpatientswithcardiacsyndromex AT baycanomerfaruk serumprolidaseactivityinpatientswithcardiacsyndromex AT kocakmehmet serumprolidaseactivityinpatientswithcardiacsyndromex AT kulseref serumprolidaseactivityinpatientswithcardiacsyndromex |