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
Autor(a) principal: | |
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Data de Publicação: | 2000 |
Outros Autores: | , , , , , |
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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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 |
_version_ |
1814268340742389760 |