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The diagnostic role of glycosaminoglycans in pleural effusions: A pilot study
BACKGROUND: Pleural effusions are classified into transudates and exudates. Various criteria have been used with Light's et al being the most accepted ones. Glycosaminoglycans (GAGs) have been detected during pleural fluids (PF) analysis in various causes. In this pilot study, we investigated:...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657101/ https://www.ncbi.nlm.nih.gov/pubmed/19226451 http://dx.doi.org/10.1186/1471-2466-9-9 |
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author | Vavetsi, Rozina Bonovas, Stefanos Polizou, Paraskevi Papanastasopoulou, Chrysanthi Dougekou, Georgia Sitaras, Nikolaos M |
author_facet | Vavetsi, Rozina Bonovas, Stefanos Polizou, Paraskevi Papanastasopoulou, Chrysanthi Dougekou, Georgia Sitaras, Nikolaos M |
author_sort | Vavetsi, Rozina |
collection | PubMed |
description | BACKGROUND: Pleural effusions are classified into transudates and exudates. Various criteria have been used with Light's et al being the most accepted ones. Glycosaminoglycans (GAGs) have been detected during pleural fluids (PF) analysis in various causes. In this pilot study, we investigated: (a) the usefulness of GAGs in the assessment of pleural effusions, and (b) whether and in what way GAGs correlate with established criteria used to indicate an exudate. METHODS: LDH, total protein, cholesterol and GAG levels were measured in pleural fluid and serum from 50 patients with pleural effusion. GAG levels were defined by the photometric method of Hata. The discriminative properties of pleural GAGs (pGAG), pleural fluid/serum GAG ratio (GAGR), serum GAGs (sGAG) and serum LDH (sLDH) were explored with ROC analysis. RESULTS: According to ROC analysis, pGAG and GAGR exhibited satisfactory discriminative properties in the separation of pleural effusions. For GAGR, at a 1.1 cut off point, sensitivity and specificity reached 75.6%; 95%CI: 60.5–87.1 and 100%; 95%CI: 47.8–100, respectively. For pGAG at a cut off value of 8.4 μg/ml, these percentages changed to 86.7%; 95%CI: 73.2–94.9 and 100%; 95%CI: 47.8–100. The study also revealed the differential role of sGAG between malignancies and benign cases, scoring 68.8%; 95%CI: 50.0–83.9 for sensitivity, and 84.6%; 95%CI: 54.5–97.6 for specificity at a 7.8 μg/ml cut off. CONCLUSION: Our results suggest that glycosaminoglycan measurement of both serum and pleural effusions could be useful for simultaneous differentiation of exudates from transudates, and of malignant from benign exudates. |
format | Text |
id | pubmed-2657101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26571012009-03-18 The diagnostic role of glycosaminoglycans in pleural effusions: A pilot study Vavetsi, Rozina Bonovas, Stefanos Polizou, Paraskevi Papanastasopoulou, Chrysanthi Dougekou, Georgia Sitaras, Nikolaos M BMC Pulm Med Research Article BACKGROUND: Pleural effusions are classified into transudates and exudates. Various criteria have been used with Light's et al being the most accepted ones. Glycosaminoglycans (GAGs) have been detected during pleural fluids (PF) analysis in various causes. In this pilot study, we investigated: (a) the usefulness of GAGs in the assessment of pleural effusions, and (b) whether and in what way GAGs correlate with established criteria used to indicate an exudate. METHODS: LDH, total protein, cholesterol and GAG levels were measured in pleural fluid and serum from 50 patients with pleural effusion. GAG levels were defined by the photometric method of Hata. The discriminative properties of pleural GAGs (pGAG), pleural fluid/serum GAG ratio (GAGR), serum GAGs (sGAG) and serum LDH (sLDH) were explored with ROC analysis. RESULTS: According to ROC analysis, pGAG and GAGR exhibited satisfactory discriminative properties in the separation of pleural effusions. For GAGR, at a 1.1 cut off point, sensitivity and specificity reached 75.6%; 95%CI: 60.5–87.1 and 100%; 95%CI: 47.8–100, respectively. For pGAG at a cut off value of 8.4 μg/ml, these percentages changed to 86.7%; 95%CI: 73.2–94.9 and 100%; 95%CI: 47.8–100. The study also revealed the differential role of sGAG between malignancies and benign cases, scoring 68.8%; 95%CI: 50.0–83.9 for sensitivity, and 84.6%; 95%CI: 54.5–97.6 for specificity at a 7.8 μg/ml cut off. CONCLUSION: Our results suggest that glycosaminoglycan measurement of both serum and pleural effusions could be useful for simultaneous differentiation of exudates from transudates, and of malignant from benign exudates. BioMed Central 2009-02-18 /pmc/articles/PMC2657101/ /pubmed/19226451 http://dx.doi.org/10.1186/1471-2466-9-9 Text en Copyright © 2009 Vavetsi 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 cited. |
spellingShingle | Research Article Vavetsi, Rozina Bonovas, Stefanos Polizou, Paraskevi Papanastasopoulou, Chrysanthi Dougekou, Georgia Sitaras, Nikolaos M The diagnostic role of glycosaminoglycans in pleural effusions: A pilot study |
title | The diagnostic role of glycosaminoglycans in pleural effusions: A pilot study |
title_full | The diagnostic role of glycosaminoglycans in pleural effusions: A pilot study |
title_fullStr | The diagnostic role of glycosaminoglycans in pleural effusions: A pilot study |
title_full_unstemmed | The diagnostic role of glycosaminoglycans in pleural effusions: A pilot study |
title_short | The diagnostic role of glycosaminoglycans in pleural effusions: A pilot study |
title_sort | diagnostic role of glycosaminoglycans in pleural effusions: a pilot study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657101/ https://www.ncbi.nlm.nih.gov/pubmed/19226451 http://dx.doi.org/10.1186/1471-2466-9-9 |
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