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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...

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Autores principales: Bílek, Radovan, Vlček, Petr, Šafařík, Libor, Michalský, David, Novák, Květoslav, Dušková, Jaroslava, Václavíková, Eliška, Widimský, Jiří, Zelinka, Tomáš
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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.
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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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