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...

Descripción completa

Detalles Bibliográficos
Autores principales: Aciksari, Gonul, Demir, Bulent, Uygun, Turgut, Gedikbasi, Asuman, Kutlu, Orkide, Atici, Adem, Baycan, Omer Faruk, Kocak, Mehmet, Kul, Seref
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