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Could elevated platelet-lymphocyte ratio predict left ventricular systolic dysfunction in patients with non-ST elevated acute coronary syndrome?

OBJECTIVE: The prognostic value of a high platelet-lymphocyte ratio (PLR) has been reported in patients with non-ST elevated myocardial infarction (NSTEMI) and different oncologic disorders. We aimed to evaluate the predictive value of the PLR for left ventricular systolic dysfunction (LVSD) in pati...

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Autores principales: Bekler, Adem, Gazi, Emine, Yılmaz, Mustafa, Temiz, Ahmet, Altun, Burak, Barutçu, Ahmet, Peker, Tezcan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779175/
https://www.ncbi.nlm.nih.gov/pubmed/25430405
http://dx.doi.org/10.5152/akd.2014.5434
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author Bekler, Adem
Gazi, Emine
Yılmaz, Mustafa
Temiz, Ahmet
Altun, Burak
Barutçu, Ahmet
Peker, Tezcan
author_facet Bekler, Adem
Gazi, Emine
Yılmaz, Mustafa
Temiz, Ahmet
Altun, Burak
Barutçu, Ahmet
Peker, Tezcan
author_sort Bekler, Adem
collection PubMed
description OBJECTIVE: The prognostic value of a high platelet-lymphocyte ratio (PLR) has been reported in patients with non-ST elevated myocardial infarction (NSTEMI) and different oncologic disorders. We aimed to evaluate the predictive value of the PLR for left ventricular systolic dysfunction (LVSD) in patients with non-ST elevated acute coronary syndrome (NST-ACS). METHODS: A total of 220 patients with NST-ACS were included in the study. The study population was divided into tertiles based on admission PLR values. High (n=73) and low PLR (n=147) groups were defined as patients having values in the third tertile (>135.6) and lower 2 tertiles (≤135.6), respectively. Left ventricular dysfunction was defined as ejection fraction ≤40%, and related variables were evaluated by backward conditional binary logistic regression analysis. RESULTS: The patients in the high PLR group were older (p<0.001) and had a higher rate of previous myocardial infarction and NSTEMI (p=0.046, p=0.013, respectively). There were significantly more coronary arteries narrowed (p=0.001) and lower left ventricular ejection fraction (p<0.001) in the high PLR group. Baseline platelet levels were significantly higher (p<0.001) and triglyceride and lymphocyte levels were significantly lower (p=0.009 and p<0.001, respectively) in the high PLR group. PLR >135.6 was found to be an independent predictor of systolic dysfunction in the multivariate analyses (ß: 0.306, 95% confidence interval: 0.151-0.619; p=0.001). CONCLUSION: A high PLR is a strong and independent predictor for LVSD in patients with NST-ACS.
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spelling pubmed-57791752018-01-26 Could elevated platelet-lymphocyte ratio predict left ventricular systolic dysfunction in patients with non-ST elevated acute coronary syndrome? Bekler, Adem Gazi, Emine Yılmaz, Mustafa Temiz, Ahmet Altun, Burak Barutçu, Ahmet Peker, Tezcan Anatol J Cardiol Original Investigation OBJECTIVE: The prognostic value of a high platelet-lymphocyte ratio (PLR) has been reported in patients with non-ST elevated myocardial infarction (NSTEMI) and different oncologic disorders. We aimed to evaluate the predictive value of the PLR for left ventricular systolic dysfunction (LVSD) in patients with non-ST elevated acute coronary syndrome (NST-ACS). METHODS: A total of 220 patients with NST-ACS were included in the study. The study population was divided into tertiles based on admission PLR values. High (n=73) and low PLR (n=147) groups were defined as patients having values in the third tertile (>135.6) and lower 2 tertiles (≤135.6), respectively. Left ventricular dysfunction was defined as ejection fraction ≤40%, and related variables were evaluated by backward conditional binary logistic regression analysis. RESULTS: The patients in the high PLR group were older (p<0.001) and had a higher rate of previous myocardial infarction and NSTEMI (p=0.046, p=0.013, respectively). There were significantly more coronary arteries narrowed (p=0.001) and lower left ventricular ejection fraction (p<0.001) in the high PLR group. Baseline platelet levels were significantly higher (p<0.001) and triglyceride and lymphocyte levels were significantly lower (p=0.009 and p<0.001, respectively) in the high PLR group. PLR >135.6 was found to be an independent predictor of systolic dysfunction in the multivariate analyses (ß: 0.306, 95% confidence interval: 0.151-0.619; p=0.001). CONCLUSION: A high PLR is a strong and independent predictor for LVSD in patients with NST-ACS. Kare Publishing 2015-05 2014-04-16 /pmc/articles/PMC5779175/ /pubmed/25430405 http://dx.doi.org/10.5152/akd.2014.5434 Text en Copyright © 2015 Turkish Society of Cardiology 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 Investigation
Bekler, Adem
Gazi, Emine
Yılmaz, Mustafa
Temiz, Ahmet
Altun, Burak
Barutçu, Ahmet
Peker, Tezcan
Could elevated platelet-lymphocyte ratio predict left ventricular systolic dysfunction in patients with non-ST elevated acute coronary syndrome?
title Could elevated platelet-lymphocyte ratio predict left ventricular systolic dysfunction in patients with non-ST elevated acute coronary syndrome?
title_full Could elevated platelet-lymphocyte ratio predict left ventricular systolic dysfunction in patients with non-ST elevated acute coronary syndrome?
title_fullStr Could elevated platelet-lymphocyte ratio predict left ventricular systolic dysfunction in patients with non-ST elevated acute coronary syndrome?
title_full_unstemmed Could elevated platelet-lymphocyte ratio predict left ventricular systolic dysfunction in patients with non-ST elevated acute coronary syndrome?
title_short Could elevated platelet-lymphocyte ratio predict left ventricular systolic dysfunction in patients with non-ST elevated acute coronary syndrome?
title_sort could elevated platelet-lymphocyte ratio predict left ventricular systolic dysfunction in patients with non-st elevated acute coronary syndrome?
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779175/
https://www.ncbi.nlm.nih.gov/pubmed/25430405
http://dx.doi.org/10.5152/akd.2014.5434
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