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Mean platelet volume as an inflammation marker in active pulmonary tuberculosis
BACKGROUND: The mean platelet volume (MPV) reflects the size of platelets. It has been shown to be inversely correlated with level of the inflammation in some chronic inflammatory diseases. This prospective study aims to show the usability of MPV as an inflammation marker in patients with active pul...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995664/ https://www.ncbi.nlm.nih.gov/pubmed/24581084 http://dx.doi.org/10.1186/2049-6958-9-11 |
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author | Gunluoglu, Gulsah Yazar, Esra Ertan Veske, Nurdan Simsek Seyhan, Ekrem Cengiz Altin, Sedat |
author_facet | Gunluoglu, Gulsah Yazar, Esra Ertan Veske, Nurdan Simsek Seyhan, Ekrem Cengiz Altin, Sedat |
author_sort | Gunluoglu, Gulsah |
collection | PubMed |
description | BACKGROUND: The mean platelet volume (MPV) reflects the size of platelets. It has been shown to be inversely correlated with level of the inflammation in some chronic inflammatory diseases. This prospective study aims to show the usability of MPV as an inflammation marker in patients with active pulmonary tuberculosis (PTB) by comparison with healthy controls. In addition, its relationships with other inflammatory markers such as C-reactive protein (CRP) and the erythrocyte sedimentation rate (ESR) as well as with the radiological extent of disease were examined. METHODS: This study included 82 patients with active PTB and 95 healthy subjects (control group). Whole blood counts, CRP level, and ESR were compared between the two groups. In the PTB group, the relationships between the radiological extent of disease and the MPV and other inflammation markers were investigated. RESULTS: The MPV was 7.74 ± 1.33/μL in the PTB group and 8.20 ± 1.13/μL in the control group (p = 0.005). The blood platelet count, CRP level, and ESR were significantly higher in the active PTB group than in the control group (p < 0.0001). In the PTB group, CRP levels (r = 0.26, p = 0.003) and ESR (r = 0.39, p = 0.003), but not MPV (p = 0.80), were significantly correlated with the radiologic extent of the disease. CONCLUSIONS: The MPV was lower in patients with PTB than in healthy controls, however, the difference was limited. The MPV does not reflect the severity of the disease. The use of MPV as an inflammation marker and a negative acute-phase reactant in PTB does not seem to be reliable. |
format | Online Article Text |
id | pubmed-3995664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39956642014-04-23 Mean platelet volume as an inflammation marker in active pulmonary tuberculosis Gunluoglu, Gulsah Yazar, Esra Ertan Veske, Nurdan Simsek Seyhan, Ekrem Cengiz Altin, Sedat Multidiscip Respir Med Original Research Article BACKGROUND: The mean platelet volume (MPV) reflects the size of platelets. It has been shown to be inversely correlated with level of the inflammation in some chronic inflammatory diseases. This prospective study aims to show the usability of MPV as an inflammation marker in patients with active pulmonary tuberculosis (PTB) by comparison with healthy controls. In addition, its relationships with other inflammatory markers such as C-reactive protein (CRP) and the erythrocyte sedimentation rate (ESR) as well as with the radiological extent of disease were examined. METHODS: This study included 82 patients with active PTB and 95 healthy subjects (control group). Whole blood counts, CRP level, and ESR were compared between the two groups. In the PTB group, the relationships between the radiological extent of disease and the MPV and other inflammation markers were investigated. RESULTS: The MPV was 7.74 ± 1.33/μL in the PTB group and 8.20 ± 1.13/μL in the control group (p = 0.005). The blood platelet count, CRP level, and ESR were significantly higher in the active PTB group than in the control group (p < 0.0001). In the PTB group, CRP levels (r = 0.26, p = 0.003) and ESR (r = 0.39, p = 0.003), but not MPV (p = 0.80), were significantly correlated with the radiologic extent of the disease. CONCLUSIONS: The MPV was lower in patients with PTB than in healthy controls, however, the difference was limited. The MPV does not reflect the severity of the disease. The use of MPV as an inflammation marker and a negative acute-phase reactant in PTB does not seem to be reliable. BioMed Central 2014-02-28 /pmc/articles/PMC3995664/ /pubmed/24581084 http://dx.doi.org/10.1186/2049-6958-9-11 Text en Copyright © 2014 Gunluoglu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Original Research Article Gunluoglu, Gulsah Yazar, Esra Ertan Veske, Nurdan Simsek Seyhan, Ekrem Cengiz Altin, Sedat Mean platelet volume as an inflammation marker in active pulmonary tuberculosis |
title | Mean platelet volume as an inflammation marker in active pulmonary tuberculosis |
title_full | Mean platelet volume as an inflammation marker in active pulmonary tuberculosis |
title_fullStr | Mean platelet volume as an inflammation marker in active pulmonary tuberculosis |
title_full_unstemmed | Mean platelet volume as an inflammation marker in active pulmonary tuberculosis |
title_short | Mean platelet volume as an inflammation marker in active pulmonary tuberculosis |
title_sort | mean platelet volume as an inflammation marker in active pulmonary tuberculosis |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995664/ https://www.ncbi.nlm.nih.gov/pubmed/24581084 http://dx.doi.org/10.1186/2049-6958-9-11 |
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