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Evaluation of Red Blood Cell Distribution Width in Patients with Cardiac Syndrome X
BACKGROUND: Cardiac syndrome X (CSX) is a condition characterized by chest pain with normal coronary arteries. However, its pathogenesis has not fully been understood yet. Red blood cell distribution width (RDW) has recently been suggested as a marker of acute and chronic cardiovascular diseases, wh...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810111/ https://www.ncbi.nlm.nih.gov/pubmed/23478272 http://dx.doi.org/10.3233/DMA-130977 |
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author | Qing, Ping Luo, Song-Hui Guo, Yuan-Lin Liu, Jun Xu, Rui-Xia Zhu, Cheng-Gang Jia, Yan-Jun Ma, Feng-Lian Wu, Na-Qiong Jiang, Li-Xin Li, Jian-Jun |
author_facet | Qing, Ping Luo, Song-Hui Guo, Yuan-Lin Liu, Jun Xu, Rui-Xia Zhu, Cheng-Gang Jia, Yan-Jun Ma, Feng-Lian Wu, Na-Qiong Jiang, Li-Xin Li, Jian-Jun |
author_sort | Qing, Ping |
collection | PubMed |
description | BACKGROUND: Cardiac syndrome X (CSX) is a condition characterized by chest pain with normal coronary arteries. However, its pathogenesis has not fully been understood yet. Red blood cell distribution width (RDW) has recently been suggested as a marker of acute and chronic cardiovascular diseases, while no data is available in patients with CSX. METHODS: One hundred and twenty consecutive patients with CSX and 102 normal controls were prospectively enrolled in this study. Blood samples were drawn from all individuals for measuring RDW and high-sensitivity C-reactive protein (CRP). The baseline data were compared between patients with CSX and normal controls. RESULTS: The RDW levels were significantly higher in patients with CSX than that in those with normal controls (13.1 ± 2.1 versus 12.3 ± 1.8, p = 0.011). Moreover, the data showed that the levels of plasma CRP were marked higher in patients with CSX than those that were observed in normal controls (CRP: 2.8 ± 2.2 mg/L versus 2.0 ± 1.7 mg/dl, p = 0.014). In addition, the multivariate analysis indicated that peripheral monocyte cell, CRP and RDW were the independent variables most strongly associated with CSX. In a receiver operating characteristic (ROC) curve analysis, we found that an RDW value of 12.8% was used as an effective cut-point in the segregation of the presence or absence of cardiac syndrome X, a sensitivity of 52.0% and a specificity of 65.4% were obtained. Finally, correlation analysis suggested that there was positive correlation between plasma levels of CRP and RDW levels (n = 120, γ = 0.381, P = 0.013). CONCLUSIONS: The present study, for the first time, demonstrated that elevated RDW and CRP levels were independently associated with the presence of CSX. |
format | Online Article Text |
id | pubmed-3810111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38101112013-12-02 Evaluation of Red Blood Cell Distribution Width in Patients with Cardiac Syndrome X Qing, Ping Luo, Song-Hui Guo, Yuan-Lin Liu, Jun Xu, Rui-Xia Zhu, Cheng-Gang Jia, Yan-Jun Ma, Feng-Lian Wu, Na-Qiong Jiang, Li-Xin Li, Jian-Jun Dis Markers Other BACKGROUND: Cardiac syndrome X (CSX) is a condition characterized by chest pain with normal coronary arteries. However, its pathogenesis has not fully been understood yet. Red blood cell distribution width (RDW) has recently been suggested as a marker of acute and chronic cardiovascular diseases, while no data is available in patients with CSX. METHODS: One hundred and twenty consecutive patients with CSX and 102 normal controls were prospectively enrolled in this study. Blood samples were drawn from all individuals for measuring RDW and high-sensitivity C-reactive protein (CRP). The baseline data were compared between patients with CSX and normal controls. RESULTS: The RDW levels were significantly higher in patients with CSX than that in those with normal controls (13.1 ± 2.1 versus 12.3 ± 1.8, p = 0.011). Moreover, the data showed that the levels of plasma CRP were marked higher in patients with CSX than those that were observed in normal controls (CRP: 2.8 ± 2.2 mg/L versus 2.0 ± 1.7 mg/dl, p = 0.014). In addition, the multivariate analysis indicated that peripheral monocyte cell, CRP and RDW were the independent variables most strongly associated with CSX. In a receiver operating characteristic (ROC) curve analysis, we found that an RDW value of 12.8% was used as an effective cut-point in the segregation of the presence or absence of cardiac syndrome X, a sensitivity of 52.0% and a specificity of 65.4% were obtained. Finally, correlation analysis suggested that there was positive correlation between plasma levels of CRP and RDW levels (n = 120, γ = 0.381, P = 0.013). CONCLUSIONS: The present study, for the first time, demonstrated that elevated RDW and CRP levels were independently associated with the presence of CSX. IOS Press 2013 2013-05-21 /pmc/articles/PMC3810111/ /pubmed/23478272 http://dx.doi.org/10.3233/DMA-130977 Text en Copyright © 2013 Hindawi Publishing Corporation. |
spellingShingle | Other Qing, Ping Luo, Song-Hui Guo, Yuan-Lin Liu, Jun Xu, Rui-Xia Zhu, Cheng-Gang Jia, Yan-Jun Ma, Feng-Lian Wu, Na-Qiong Jiang, Li-Xin Li, Jian-Jun Evaluation of Red Blood Cell Distribution Width in Patients with Cardiac Syndrome X |
title | Evaluation of Red Blood Cell Distribution Width in Patients with Cardiac Syndrome X |
title_full | Evaluation of Red Blood Cell Distribution Width in Patients with Cardiac Syndrome X |
title_fullStr | Evaluation of Red Blood Cell Distribution Width in Patients with Cardiac Syndrome X |
title_full_unstemmed | Evaluation of Red Blood Cell Distribution Width in Patients with Cardiac Syndrome X |
title_short | Evaluation of Red Blood Cell Distribution Width in Patients with Cardiac Syndrome X |
title_sort | evaluation of red blood cell distribution width in patients with cardiac syndrome x |
topic | Other |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810111/ https://www.ncbi.nlm.nih.gov/pubmed/23478272 http://dx.doi.org/10.3233/DMA-130977 |
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