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Chromogranin A in the Laboratory Diagnosis of Pheochromocytoma and Paraganglioma
This work discusses the clinical performance of chromogranin A (CGA), a commonly measured marker in neuroendocrine neoplasms, for the diagnosis of pheochromocytoma/paraganglioma (PPGL). Plasma CGA (cut-off value 150 µg/L) was determined by an immunoradiometric assay. Free metanephrine (cut-off value...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521298/ https://www.ncbi.nlm.nih.gov/pubmed/31027285 http://dx.doi.org/10.3390/cancers11040586 |
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author | Bílek, Radovan Vlček, Petr Šafařík, Libor Michalský, David Novák, Květoslav Dušková, Jaroslava Václavíková, Eliška Widimský, Jiří Zelinka, Tomáš |
author_facet | Bílek, Radovan Vlček, Petr Šafařík, Libor Michalský, David Novák, Květoslav Dušková, Jaroslava Václavíková, Eliška Widimský, Jiří Zelinka, Tomáš |
author_sort | Bílek, Radovan |
collection | PubMed |
description | This work discusses the clinical performance of chromogranin A (CGA), a commonly measured marker in neuroendocrine neoplasms, for the diagnosis of pheochromocytoma/paraganglioma (PPGL). Plasma CGA (cut-off value 150 µg/L) was determined by an immunoradiometric assay. Free metanephrine (cut-off value 100 ng/L) and normetanephrine (cut-off value 170 ng/L) were determined by radioimmunoassay. Blood samples were collected from PPGL patients preoperatively, one week, six months, one year and two years after adrenal gland surgery. The control patients not diagnosed with PPGL suffered from adrenal problems or from MEN2 and thyroid carcinoma. The clinical sensitivity in the PPGL group of patients (n = 71) based on CGA is 90% and is below the clinical sensitivity determined by metanephrines (97%). The clinical specificity based on all plasma CGA values after surgery (n = 98) is 99% and is the same for metanephrines assays. The clinical specificity of CGA in the control group (n = 85) was 92% or 99% using metanephrines tests. We can conclude that plasma CGA can serve as an appropriate complement to metanephrines assays in laboratory diagnosis of PPGL patients. CGA is elevated in PPGLs, as well as in other neuroendocrine or non-neuroendocrine neoplasia and under clinical conditions increasing adrenergic activity. |
format | Online Article Text |
id | pubmed-6521298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65212982019-05-31 Chromogranin A in the Laboratory Diagnosis of Pheochromocytoma and Paraganglioma Bílek, Radovan Vlček, Petr Šafařík, Libor Michalský, David Novák, Květoslav Dušková, Jaroslava Václavíková, Eliška Widimský, Jiří Zelinka, Tomáš Cancers (Basel) Article This work discusses the clinical performance of chromogranin A (CGA), a commonly measured marker in neuroendocrine neoplasms, for the diagnosis of pheochromocytoma/paraganglioma (PPGL). Plasma CGA (cut-off value 150 µg/L) was determined by an immunoradiometric assay. Free metanephrine (cut-off value 100 ng/L) and normetanephrine (cut-off value 170 ng/L) were determined by radioimmunoassay. Blood samples were collected from PPGL patients preoperatively, one week, six months, one year and two years after adrenal gland surgery. The control patients not diagnosed with PPGL suffered from adrenal problems or from MEN2 and thyroid carcinoma. The clinical sensitivity in the PPGL group of patients (n = 71) based on CGA is 90% and is below the clinical sensitivity determined by metanephrines (97%). The clinical specificity based on all plasma CGA values after surgery (n = 98) is 99% and is the same for metanephrines assays. The clinical specificity of CGA in the control group (n = 85) was 92% or 99% using metanephrines tests. We can conclude that plasma CGA can serve as an appropriate complement to metanephrines assays in laboratory diagnosis of PPGL patients. CGA is elevated in PPGLs, as well as in other neuroendocrine or non-neuroendocrine neoplasia and under clinical conditions increasing adrenergic activity. MDPI 2019-04-25 /pmc/articles/PMC6521298/ /pubmed/31027285 http://dx.doi.org/10.3390/cancers11040586 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bílek, Radovan Vlček, Petr Šafařík, Libor Michalský, David Novák, Květoslav Dušková, Jaroslava Václavíková, Eliška Widimský, Jiří Zelinka, Tomáš Chromogranin A in the Laboratory Diagnosis of Pheochromocytoma and Paraganglioma |
title | Chromogranin A in the Laboratory Diagnosis of Pheochromocytoma and Paraganglioma |
title_full | Chromogranin A in the Laboratory Diagnosis of Pheochromocytoma and Paraganglioma |
title_fullStr | Chromogranin A in the Laboratory Diagnosis of Pheochromocytoma and Paraganglioma |
title_full_unstemmed | Chromogranin A in the Laboratory Diagnosis of Pheochromocytoma and Paraganglioma |
title_short | Chromogranin A in the Laboratory Diagnosis of Pheochromocytoma and Paraganglioma |
title_sort | chromogranin a in the laboratory diagnosis of pheochromocytoma and paraganglioma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521298/ https://www.ncbi.nlm.nih.gov/pubmed/31027285 http://dx.doi.org/10.3390/cancers11040586 |
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