Macrocalcitonin Is a Novel Pitfall in the Routine of Serum Calcitonin Immunoassay
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1210/jc.2015-3137 https://repositorio.unifesp.br/handle/11600/57993 |
Resumo: | Context: Calcitonin (CT) is a sensitive marker of medullary thyroid carcinoma (MTC) and is used for primary diagnosis and follow-up after thyroidectomy. However, persistently elevated CT is observed even after complete surgical removal without evidence of a recurrent or persistent tumor. Objective: To investigate the presence of assay interference in the serum CT of MTC patients who are apparently without a structural disease. Patients and Methods: We studied three index MTC cases for CT assay interference and 14 patients with metastatic MTC. The CT level was measured using an immunofluorometric assay. Screening for assay interference was performed by determination of CT levels before and after serum treatment with polyethylene glycol. Additionally, samples were analyzed by chromatography on ultra-performance liquid chromatography and protein A-Sepharose. Results: Patients with biochemical and structural disease showed CT mean recovery of 84.1% after polyethylene glycol treatment, whereas patients suspected of interference showed recovery from 2-7%. The elution profile on UPLC showed that the immunometric CT from these three patients behaved like a high molecular mass aggregate (>300 kDa). Additionally, when these samples were applied to the protein A-Sepharose, CT immunoreactivity was retained on the column and was only released after lowering the pH. Conclusions: For the first time, our results show the presence of a novel pitfall in the CT immunoassay: "macrocalcitonin." Its etiology, frequency, and meaning remain to be defined, but its recognition is of interest and can help clinicians avoid unnecessary diagnostic investigations and treatment during the follow-up of MTC. |
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Macrocalcitonin Is a Novel Pitfall in the Routine of Serum Calcitonin ImmunoassayContext: Calcitonin (CT) is a sensitive marker of medullary thyroid carcinoma (MTC) and is used for primary diagnosis and follow-up after thyroidectomy. However, persistently elevated CT is observed even after complete surgical removal without evidence of a recurrent or persistent tumor. Objective: To investigate the presence of assay interference in the serum CT of MTC patients who are apparently without a structural disease. Patients and Methods: We studied three index MTC cases for CT assay interference and 14 patients with metastatic MTC. The CT level was measured using an immunofluorometric assay. Screening for assay interference was performed by determination of CT levels before and after serum treatment with polyethylene glycol. Additionally, samples were analyzed by chromatography on ultra-performance liquid chromatography and protein A-Sepharose. Results: Patients with biochemical and structural disease showed CT mean recovery of 84.1% after polyethylene glycol treatment, whereas patients suspected of interference showed recovery from 2-7%. The elution profile on UPLC showed that the immunometric CT from these three patients behaved like a high molecular mass aggregate (>300 kDa). Additionally, when these samples were applied to the protein A-Sepharose, CT immunoreactivity was retained on the column and was only released after lowering the pH. Conclusions: For the first time, our results show the presence of a novel pitfall in the CT immunoassay: "macrocalcitonin." Its etiology, frequency, and meaning remain to be defined, but its recognition is of interest and can help clinicians avoid unnecessary diagnostic investigations and treatment during the follow-up of MTC.Univ Fed Sao Paulo, Escola Paulista Med, Div Endocrinol, Dept Med,Thyroid Dis Ctr, BR-04039032 Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Escola Paulista Med, Div Endocrinol, Dept Med,Lab Mol & Translat Endocrinol, BR-04039032 Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Escola Paulista Med, Dept Biochem, Div Mol Biol, BR-04044020 Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Escola Paulista Med, Div Endocrinol, Dept Med,Thyroid Dis Ctr, BR-04039032 Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Escola Paulista Med, Div Endocrinol, Dept Med,Lab Mol & Translat Endocrinol, BR-04039032 Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Escola Paulista Med, Dept Biochem, Div Mol Biol, BR-04044020 Sao Paulo, SP, BrazilWeb of ScienceSao Paulo State Research Foundation-FAPESPFAPESPFederal Agency of Support and Evaluation of Postgraduate Education (Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior)National Council for Scientific and Technological DevelopmentFAPESP: 2006/60402-1FAPESP: 2010/51547-1FAPESP: 2010/19478Endocrine Soc2020-08-21T17:00:26Z2020-08-21T17:00:26Z2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion653-658application/pdfhttp://dx.doi.org/10.1210/jc.2015-3137Journal Of Clinical Endocrinology & Metabolism. Washington, v. 101, n. 2, p. 653-658, 2016.10.1210/jc.2015-3137WOS000378642700035.pdf0021-972Xhttps://repositorio.unifesp.br/handle/11600/57993WOS:000378642700035engJournal Of Clinical Endocrinology & MetabolismWashingtoninfo:eu-repo/semantics/openAccessAlves, Thalita G. [UNIFESP]Kasamatsu, Teresa S. [UNIFESP]Yang, Ji H. [UNIFESP]Meneghetti, Maria Cecilia Z. [UNIFESP]Mendes, Aline [UNIFESP]Kunii, Ilda S. [UNIFESP]Lindsey, Susan C. [UNIFESP]Camacho, Cleber P. [UNIFESP]Dias da Silva, Magnus R. [UNIFESP]Maciel, Rui M. B. [UNIFESP]Vieira, Jose Gilberto H. [UNIFESP]Martins, Joao Roberto M. [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-09T10:57:55Zoai:repositorio.unifesp.br/:11600/57993Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-09T10:57:55Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Macrocalcitonin Is a Novel Pitfall in the Routine of Serum Calcitonin Immunoassay |
title |
Macrocalcitonin Is a Novel Pitfall in the Routine of Serum Calcitonin Immunoassay |
spellingShingle |
Macrocalcitonin Is a Novel Pitfall in the Routine of Serum Calcitonin Immunoassay Alves, Thalita G. [UNIFESP] |
title_short |
Macrocalcitonin Is a Novel Pitfall in the Routine of Serum Calcitonin Immunoassay |
title_full |
Macrocalcitonin Is a Novel Pitfall in the Routine of Serum Calcitonin Immunoassay |
title_fullStr |
Macrocalcitonin Is a Novel Pitfall in the Routine of Serum Calcitonin Immunoassay |
title_full_unstemmed |
Macrocalcitonin Is a Novel Pitfall in the Routine of Serum Calcitonin Immunoassay |
title_sort |
Macrocalcitonin Is a Novel Pitfall in the Routine of Serum Calcitonin Immunoassay |
author |
Alves, Thalita G. [UNIFESP] |
author_facet |
Alves, Thalita G. [UNIFESP] Kasamatsu, Teresa S. [UNIFESP] Yang, Ji H. [UNIFESP] Meneghetti, Maria Cecilia Z. [UNIFESP] Mendes, Aline [UNIFESP] Kunii, Ilda S. [UNIFESP] Lindsey, Susan C. [UNIFESP] Camacho, Cleber P. [UNIFESP] Dias da Silva, Magnus R. [UNIFESP] Maciel, Rui M. B. [UNIFESP] Vieira, Jose Gilberto H. [UNIFESP] Martins, Joao Roberto M. [UNIFESP] |
author_role |
author |
author2 |
Kasamatsu, Teresa S. [UNIFESP] Yang, Ji H. [UNIFESP] Meneghetti, Maria Cecilia Z. [UNIFESP] Mendes, Aline [UNIFESP] Kunii, Ilda S. [UNIFESP] Lindsey, Susan C. [UNIFESP] Camacho, Cleber P. [UNIFESP] Dias da Silva, Magnus R. [UNIFESP] Maciel, Rui M. B. [UNIFESP] Vieira, Jose Gilberto H. [UNIFESP] Martins, Joao Roberto M. [UNIFESP] |
author2_role |
author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Alves, Thalita G. [UNIFESP] Kasamatsu, Teresa S. [UNIFESP] Yang, Ji H. [UNIFESP] Meneghetti, Maria Cecilia Z. [UNIFESP] Mendes, Aline [UNIFESP] Kunii, Ilda S. [UNIFESP] Lindsey, Susan C. [UNIFESP] Camacho, Cleber P. [UNIFESP] Dias da Silva, Magnus R. [UNIFESP] Maciel, Rui M. B. [UNIFESP] Vieira, Jose Gilberto H. [UNIFESP] Martins, Joao Roberto M. [UNIFESP] |
description |
Context: Calcitonin (CT) is a sensitive marker of medullary thyroid carcinoma (MTC) and is used for primary diagnosis and follow-up after thyroidectomy. However, persistently elevated CT is observed even after complete surgical removal without evidence of a recurrent or persistent tumor. Objective: To investigate the presence of assay interference in the serum CT of MTC patients who are apparently without a structural disease. Patients and Methods: We studied three index MTC cases for CT assay interference and 14 patients with metastatic MTC. The CT level was measured using an immunofluorometric assay. Screening for assay interference was performed by determination of CT levels before and after serum treatment with polyethylene glycol. Additionally, samples were analyzed by chromatography on ultra-performance liquid chromatography and protein A-Sepharose. Results: Patients with biochemical and structural disease showed CT mean recovery of 84.1% after polyethylene glycol treatment, whereas patients suspected of interference showed recovery from 2-7%. The elution profile on UPLC showed that the immunometric CT from these three patients behaved like a high molecular mass aggregate (>300 kDa). Additionally, when these samples were applied to the protein A-Sepharose, CT immunoreactivity was retained on the column and was only released after lowering the pH. Conclusions: For the first time, our results show the presence of a novel pitfall in the CT immunoassay: "macrocalcitonin." Its etiology, frequency, and meaning remain to be defined, but its recognition is of interest and can help clinicians avoid unnecessary diagnostic investigations and treatment during the follow-up of MTC. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 2020-08-21T17:00:26Z 2020-08-21T17:00:26Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1210/jc.2015-3137 Journal Of Clinical Endocrinology & Metabolism. Washington, v. 101, n. 2, p. 653-658, 2016. 10.1210/jc.2015-3137 WOS000378642700035.pdf 0021-972X https://repositorio.unifesp.br/handle/11600/57993 WOS:000378642700035 |
url |
http://dx.doi.org/10.1210/jc.2015-3137 https://repositorio.unifesp.br/handle/11600/57993 |
identifier_str_mv |
Journal Of Clinical Endocrinology & Metabolism. Washington, v. 101, n. 2, p. 653-658, 2016. 10.1210/jc.2015-3137 WOS000378642700035.pdf 0021-972X WOS:000378642700035 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal Of Clinical Endocrinology & Metabolism |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
653-658 application/pdf |
dc.coverage.none.fl_str_mv |
Washington |
dc.publisher.none.fl_str_mv |
Endocrine Soc |
publisher.none.fl_str_mv |
Endocrine Soc |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268280391598080 |