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Circulating resistin protein and mRNA concentrations and clinical severity of coronary artery disease

INTRODUCTION: Previous studies have implicated a strong link between circulating plasma resistin and coronary artery disease (CAD). The aim of this study was to evaluate the differences in peripheral blood mononuclear cells (PBMC) resistin mRNA and its plasma protein concentrations between the patie...

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Autores principales: Joksic, Jelena, Sopic, Miron, Spasojevic-Kalimanovska, Vesna, Kalimanovska-Ostric, Dimitra, Andjelkovic, Kristina, Jelic-Ivanovic, Zorana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Society of Medical Biochemistry and Laboratory Medicine 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470098/
https://www.ncbi.nlm.nih.gov/pubmed/26110037
http://dx.doi.org/10.11613/BM.2015.025
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author Joksic, Jelena
Sopic, Miron
Spasojevic-Kalimanovska, Vesna
Kalimanovska-Ostric, Dimitra
Andjelkovic, Kristina
Jelic-Ivanovic, Zorana
author_facet Joksic, Jelena
Sopic, Miron
Spasojevic-Kalimanovska, Vesna
Kalimanovska-Ostric, Dimitra
Andjelkovic, Kristina
Jelic-Ivanovic, Zorana
author_sort Joksic, Jelena
collection PubMed
description INTRODUCTION: Previous studies have implicated a strong link between circulating plasma resistin and coronary artery disease (CAD). The aim of this study was to evaluate the differences in peripheral blood mononuclear cells (PBMC) resistin mRNA and its plasma protein concentrations between the patients with CAD of different clinical severity. MATERIAL AND METHODS: This study included 33 healthy subjects as the control group (CG) and 77 patients requiring coronary angiography. Of the latter 30 was CAD negative whereas 47 were CAD positive [18 with stable angina pectoris (SAP) and 29 with acute coronary syndrome (ACS)]. Circulating resistin was measured by ELISA; PBMC resistin mRNA was determined by real-time PCR. RESULTS: Resistin protein was significantly higher in the ACS group compared to the CG (P = 0.001) and the CAD negative group (P = 0.018). Resistin mRNA expression did not vary across the study groups, despite the positive correlation seen with plasma resistin (ρ = 0.305, P = 0.008). In patients, plasma resistin and PBMC resistin mRNA negatively correlated with HDL-C (ρ = -0.404, P < 0.001 and ρ = -0.257, P = 0.032, respectively). Furthermore, the highest plasma resistin tertile showed the lowest HDL-C (P = 0.006). Plasma resistin was positively associated with serum creatinine (ρ = 0.353, P = 0.002). CONCLUSION: Significant increase of plasma resistin in patients with ACS compared to CG and CAD negative patients was observed. Despite no change in PBMC resistin mRNA in different disease conditions a positive association between resistin mRNA and resistin plasma protein was evident. Both plasma resistin and PBMC resistin mRNA were negatively associated with plasma HDL-C, and plasma resistin positively with serum creatinine.
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spelling pubmed-44700982015-06-24 Circulating resistin protein and mRNA concentrations and clinical severity of coronary artery disease Joksic, Jelena Sopic, Miron Spasojevic-Kalimanovska, Vesna Kalimanovska-Ostric, Dimitra Andjelkovic, Kristina Jelic-Ivanovic, Zorana Biochem Med (Zagreb) Research Article INTRODUCTION: Previous studies have implicated a strong link between circulating plasma resistin and coronary artery disease (CAD). The aim of this study was to evaluate the differences in peripheral blood mononuclear cells (PBMC) resistin mRNA and its plasma protein concentrations between the patients with CAD of different clinical severity. MATERIAL AND METHODS: This study included 33 healthy subjects as the control group (CG) and 77 patients requiring coronary angiography. Of the latter 30 was CAD negative whereas 47 were CAD positive [18 with stable angina pectoris (SAP) and 29 with acute coronary syndrome (ACS)]. Circulating resistin was measured by ELISA; PBMC resistin mRNA was determined by real-time PCR. RESULTS: Resistin protein was significantly higher in the ACS group compared to the CG (P = 0.001) and the CAD negative group (P = 0.018). Resistin mRNA expression did not vary across the study groups, despite the positive correlation seen with plasma resistin (ρ = 0.305, P = 0.008). In patients, plasma resistin and PBMC resistin mRNA negatively correlated with HDL-C (ρ = -0.404, P < 0.001 and ρ = -0.257, P = 0.032, respectively). Furthermore, the highest plasma resistin tertile showed the lowest HDL-C (P = 0.006). Plasma resistin was positively associated with serum creatinine (ρ = 0.353, P = 0.002). CONCLUSION: Significant increase of plasma resistin in patients with ACS compared to CG and CAD negative patients was observed. Despite no change in PBMC resistin mRNA in different disease conditions a positive association between resistin mRNA and resistin plasma protein was evident. Both plasma resistin and PBMC resistin mRNA were negatively associated with plasma HDL-C, and plasma resistin positively with serum creatinine. Croatian Society of Medical Biochemistry and Laboratory Medicine 2015-06-05 /pmc/articles/PMC4470098/ /pubmed/26110037 http://dx.doi.org/10.11613/BM.2015.025 Text en
spellingShingle Research Article
Joksic, Jelena
Sopic, Miron
Spasojevic-Kalimanovska, Vesna
Kalimanovska-Ostric, Dimitra
Andjelkovic, Kristina
Jelic-Ivanovic, Zorana
Circulating resistin protein and mRNA concentrations and clinical severity of coronary artery disease
title Circulating resistin protein and mRNA concentrations and clinical severity of coronary artery disease
title_full Circulating resistin protein and mRNA concentrations and clinical severity of coronary artery disease
title_fullStr Circulating resistin protein and mRNA concentrations and clinical severity of coronary artery disease
title_full_unstemmed Circulating resistin protein and mRNA concentrations and clinical severity of coronary artery disease
title_short Circulating resistin protein and mRNA concentrations and clinical severity of coronary artery disease
title_sort circulating resistin protein and mrna concentrations and clinical severity of coronary artery disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470098/
https://www.ncbi.nlm.nih.gov/pubmed/26110037
http://dx.doi.org/10.11613/BM.2015.025
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