Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17 alpha-hydroxylase in Addison's disease and autoimmune polyendocrine syndrome type III

Detalhes bibliográficos
Autor(a) principal: Silva, R. D.
Data de Publicação: 2000
Outros Autores: Kater, Claudio Elias [UNIFESP], Dib, Sergio Atala [UNIFESP], Laureti, S., Forini, F., Cosentino, A., Falorni, A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://doi.org/10.1530/eje.0.1420187
http://repositorio.unifesp.br/handle/11600/43587
Resumo: Objective: To evaluate the frequency of autoantibodies (Ab) against 21 hydroxylase (210H), side-chain cleavage (SCC) and 17 alpha-hydroxglase (17OH), in Addison's disease (AD) and autoimmune polyendocrine syndrome type III (APSIII), Design and Methods: We used radiobinding assays and in vitro translated recombinant human S-35-21OH, S-35-SCC or S-35-17OH and studied serum samples from 29 AD (18 idiopathic, 11 granulomatous) and 18 APSIII (autoimmune thyroid disease plus type 1 diabetes mellitus, without AD) patients. Results were compared with those of adrenocortical autoantibodies obtained with indirect immunofluorescence (ACA-IIF). Results: ACA-IIF were detected in 15/18 (83%) idiopathic and in 1/11 (9%) granulomatous AD subjects. 21OHAb were found in 14/18 (78%) idiopathic and in the same (9%) granulomatous AD subject. A significant positive correlation was shown between ACA-IIF and 21OHAb levels (r(2) = 0.56, P < 0.02). The concordance rate between the two assays was 83% (24/29) in AD patients. SCCAb were found in 5/15 (28%) idiopathic (4 of whom were also positive for 21OHAb) and in the same (9%) granulomatous AD subject, 170HAb were found in only 2/18 (11%) idiopathic and none of the granulomatous AD patients. Two APSIII patients were positive for ACA-IIE but only one was positive for 210HAb and SCCAb. 170HAb were found in another two APSIII patients. Conclusions: Measurement of 210HAb should be the first step in immune assessment of patients with AD and individuals at risk for adrenal autoimmunity, in addition to ACA-IIF. Due to their low prevalence in AD, measurement of SCCAb and 170HAb should be indicated only for 210HAb negative patients and/or for those with premature ovarian failure, regardless of ACA-IIF results.
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spelling Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17 alpha-hydroxylase in Addison's disease and autoimmune polyendocrine syndrome type IIIObjective: To evaluate the frequency of autoantibodies (Ab) against 21 hydroxylase (210H), side-chain cleavage (SCC) and 17 alpha-hydroxglase (17OH), in Addison's disease (AD) and autoimmune polyendocrine syndrome type III (APSIII), Design and Methods: We used radiobinding assays and in vitro translated recombinant human S-35-21OH, S-35-SCC or S-35-17OH and studied serum samples from 29 AD (18 idiopathic, 11 granulomatous) and 18 APSIII (autoimmune thyroid disease plus type 1 diabetes mellitus, without AD) patients. Results were compared with those of adrenocortical autoantibodies obtained with indirect immunofluorescence (ACA-IIF). Results: ACA-IIF were detected in 15/18 (83%) idiopathic and in 1/11 (9%) granulomatous AD subjects. 21OHAb were found in 14/18 (78%) idiopathic and in the same (9%) granulomatous AD subject. A significant positive correlation was shown between ACA-IIF and 21OHAb levels (r(2) = 0.56, P < 0.02). The concordance rate between the two assays was 83% (24/29) in AD patients. SCCAb were found in 5/15 (28%) idiopathic (4 of whom were also positive for 21OHAb) and in the same (9%) granulomatous AD subject, 170HAb were found in only 2/18 (11%) idiopathic and none of the granulomatous AD patients. Two APSIII patients were positive for ACA-IIE but only one was positive for 210HAb and SCCAb. 170HAb were found in another two APSIII patients. Conclusions: Measurement of 210HAb should be the first step in immune assessment of patients with AD and individuals at risk for adrenal autoimmunity, in addition to ACA-IIF. Due to their low prevalence in AD, measurement of SCCAb and 170HAb should be indicated only for 210HAb negative patients and/or for those with premature ovarian failure, regardless of ACA-IIF results.Univ Fed Sao Paulo, Dept Med, Escola Paulista Med, Div Endocrinol, BR-04034970 Sao Paulo, BrazilUniv Perugia, Dept Internal Med & Endocrine & Metab Sci, I-06100 Perugia, ItalyUniv Fed Sao Paulo, Dept Med, Escola Paulista Med, Div Endocrinol, BR-04034970 Sao Paulo, BrazilWeb of ScienceScandinavian University PressUniversidade Federal de São Paulo (UNIFESP)Univ PerugiaSilva, R. D.Kater, Claudio Elias [UNIFESP]Dib, Sergio Atala [UNIFESP]Laureti, S.Forini, F.Cosentino, A.Falorni, A.2018-06-15T17:22:23Z2018-06-15T17:22:23Z2000-02-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion187-194https://doi.org/10.1530/eje.0.1420187European Journal Of Endocrinology. Oslo: Scandinavian University Press, v. 142, n. 2, p. 187-194, 2000.10.1530/eje.0.14201870804-4643http://repositorio.unifesp.br/handle/11600/43587WOS:000085405600015engEuropean Journal Of Endocrinologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-05-02T13:58:57Zoai:repositorio.unifesp.br/:11600/43587Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-05-02T13:58:57Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17 alpha-hydroxylase in Addison's disease and autoimmune polyendocrine syndrome type III
title Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17 alpha-hydroxylase in Addison's disease and autoimmune polyendocrine syndrome type III
spellingShingle Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17 alpha-hydroxylase in Addison's disease and autoimmune polyendocrine syndrome type III
Silva, R. D.
title_short Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17 alpha-hydroxylase in Addison's disease and autoimmune polyendocrine syndrome type III
title_full Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17 alpha-hydroxylase in Addison's disease and autoimmune polyendocrine syndrome type III
title_fullStr Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17 alpha-hydroxylase in Addison's disease and autoimmune polyendocrine syndrome type III
title_full_unstemmed Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17 alpha-hydroxylase in Addison's disease and autoimmune polyendocrine syndrome type III
title_sort Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17 alpha-hydroxylase in Addison's disease and autoimmune polyendocrine syndrome type III
author Silva, R. D.
author_facet Silva, R. D.
Kater, Claudio Elias [UNIFESP]
Dib, Sergio Atala [UNIFESP]
Laureti, S.
Forini, F.
Cosentino, A.
Falorni, A.
author_role author
author2 Kater, Claudio Elias [UNIFESP]
Dib, Sergio Atala [UNIFESP]
Laureti, S.
Forini, F.
Cosentino, A.
Falorni, A.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Univ Perugia
dc.contributor.author.fl_str_mv Silva, R. D.
Kater, Claudio Elias [UNIFESP]
Dib, Sergio Atala [UNIFESP]
Laureti, S.
Forini, F.
Cosentino, A.
Falorni, A.
description Objective: To evaluate the frequency of autoantibodies (Ab) against 21 hydroxylase (210H), side-chain cleavage (SCC) and 17 alpha-hydroxglase (17OH), in Addison's disease (AD) and autoimmune polyendocrine syndrome type III (APSIII), Design and Methods: We used radiobinding assays and in vitro translated recombinant human S-35-21OH, S-35-SCC or S-35-17OH and studied serum samples from 29 AD (18 idiopathic, 11 granulomatous) and 18 APSIII (autoimmune thyroid disease plus type 1 diabetes mellitus, without AD) patients. Results were compared with those of adrenocortical autoantibodies obtained with indirect immunofluorescence (ACA-IIF). Results: ACA-IIF were detected in 15/18 (83%) idiopathic and in 1/11 (9%) granulomatous AD subjects. 21OHAb were found in 14/18 (78%) idiopathic and in the same (9%) granulomatous AD subject. A significant positive correlation was shown between ACA-IIF and 21OHAb levels (r(2) = 0.56, P < 0.02). The concordance rate between the two assays was 83% (24/29) in AD patients. SCCAb were found in 5/15 (28%) idiopathic (4 of whom were also positive for 21OHAb) and in the same (9%) granulomatous AD subject, 170HAb were found in only 2/18 (11%) idiopathic and none of the granulomatous AD patients. Two APSIII patients were positive for ACA-IIE but only one was positive for 210HAb and SCCAb. 170HAb were found in another two APSIII patients. Conclusions: Measurement of 210HAb should be the first step in immune assessment of patients with AD and individuals at risk for adrenal autoimmunity, in addition to ACA-IIF. Due to their low prevalence in AD, measurement of SCCAb and 170HAb should be indicated only for 210HAb negative patients and/or for those with premature ovarian failure, regardless of ACA-IIF results.
publishDate 2000
dc.date.none.fl_str_mv 2000-02-01
2018-06-15T17:22:23Z
2018-06-15T17:22:23Z
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 https://doi.org/10.1530/eje.0.1420187
European Journal Of Endocrinology. Oslo: Scandinavian University Press, v. 142, n. 2, p. 187-194, 2000.
10.1530/eje.0.1420187
0804-4643
http://repositorio.unifesp.br/handle/11600/43587
WOS:000085405600015
url https://doi.org/10.1530/eje.0.1420187
http://repositorio.unifesp.br/handle/11600/43587
identifier_str_mv European Journal Of Endocrinology. Oslo: Scandinavian University Press, v. 142, n. 2, p. 187-194, 2000.
10.1530/eje.0.1420187
0804-4643
WOS:000085405600015
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv European Journal Of Endocrinology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 187-194
dc.publisher.none.fl_str_mv Scandinavian University Press
publisher.none.fl_str_mv Scandinavian University Press
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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