Methacholine vs adenosine on intra and extrathoracic airway hyperresponsiveness in patients with cough variant asthma
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1111/j.1398-9995.2007.01589.x http://repositorio.unifesp.br/handle/11600/30616 |
Resumo: | Background: Airway hyperresponsiveness (AHR) can be studied by bronchoprovocation test (BPT) using direct (methacholine - MCh) or indirect (adenosine 5'-monophosphate - AMP) stimuli. These two substances have not been compared in cough variant asthma (CVA).Objective: We designed a randomized, single-blind, cross-over study to compare AMP and MCh in the detection of CVA. Additionally, we examined whether assessment of extrathoracic airway hyperresponsiveness (EAHR) during MCh and AMP helped in the evaluation of CVA.Methods: Patients with CVA with previous positive MCh BPT performed challenges with AMP and MCh. the variables were: (i) a provocative dose producing a 20% fall in forced expiratory volume in 1 s (FEV(1)) value (PD(20)MCh); (ii) a provocative dose producing a 25% fall in the maximal mid-inspiratory flow (FIF(50)) from baseline (PD(25)MCh) for MCh; (iii) a provocative concentration producing a 20% fall in FEV(1) value (PC(20)AMP) and (iv) a provocative concentration producing a 25% fall in the FIF(50) from baseline (PC(25)AMP) for AMP.Results: All 113 patients with CVA responded to PD(20)MCh and 96% and 69% responded to PC(20)AMP, if we used PC(20) <= 200 mg/ml or PC(20) <= 100 mg/ml, respectively, with an excellent correlation between these two tests (r = 0.87 and 0.76, respectively). Extrathoracic AHR associated with AHR was found in 10% in MCh challenge and in 11% with AMP challenge and no patients had EAHR alone.Conclusion: Adenosine challenges correlate well with MCh in patients with CVA. A minority (c. 10%) of CVA patients have EAHR as measured by these tests, while most had AHR as assessed with each of the challenge agents. |
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Methacholine vs adenosine on intra and extrathoracic airway hyperresponsiveness in patients with cough variant asthmaBackground: Airway hyperresponsiveness (AHR) can be studied by bronchoprovocation test (BPT) using direct (methacholine - MCh) or indirect (adenosine 5'-monophosphate - AMP) stimuli. These two substances have not been compared in cough variant asthma (CVA).Objective: We designed a randomized, single-blind, cross-over study to compare AMP and MCh in the detection of CVA. Additionally, we examined whether assessment of extrathoracic airway hyperresponsiveness (EAHR) during MCh and AMP helped in the evaluation of CVA.Methods: Patients with CVA with previous positive MCh BPT performed challenges with AMP and MCh. the variables were: (i) a provocative dose producing a 20% fall in forced expiratory volume in 1 s (FEV(1)) value (PD(20)MCh); (ii) a provocative dose producing a 25% fall in the maximal mid-inspiratory flow (FIF(50)) from baseline (PD(25)MCh) for MCh; (iii) a provocative concentration producing a 20% fall in FEV(1) value (PC(20)AMP) and (iv) a provocative concentration producing a 25% fall in the FIF(50) from baseline (PC(25)AMP) for AMP.Results: All 113 patients with CVA responded to PD(20)MCh and 96% and 69% responded to PC(20)AMP, if we used PC(20) <= 200 mg/ml or PC(20) <= 100 mg/ml, respectively, with an excellent correlation between these two tests (r = 0.87 and 0.76, respectively). Extrathoracic AHR associated with AHR was found in 10% in MCh challenge and in 11% with AMP challenge and no patients had EAHR alone.Conclusion: Adenosine challenges correlate well with MCh in patients with CVA. A minority (c. 10%) of CVA patients have EAHR as measured by these tests, while most had AHR as assessed with each of the challenge agents.Universidade Federal de São Paulo, UNIFESP, Dept Med, Div Resp, BR-01228000 São Paulo, SP, BrazilUniversidade Federal de São Paulo, UNIFESP, Dept Med, Div Resp, BR-01228000 São Paulo, SP, BrazilWeb of ScienceWiley-BlackwellUniversidade Federal de São Paulo (UNIFESP)Ribeiro, M. [UNIFESP]Pereira, C. A. C. [UNIFESP]Nery, L. E. [UNIFESP]Beppu, O. S. [UNIFESP]Silva, C. O. S. [UNIFESP]2016-01-24T13:49:46Z2016-01-24T13:49:46Z2008-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion527-532http://dx.doi.org/10.1111/j.1398-9995.2007.01589.xAllergy. Malden: Wiley-Blackwell Publishing, Inc, v. 63, n. 5, p. 527-532, 2008.10.1111/j.1398-9995.2007.01589.x0105-4538http://repositorio.unifesp.br/handle/11600/30616WOS:000254638700006engAllergyinfo:eu-repo/semantics/openAccesshttp://olabout.wiley.com/WileyCDA/Section/id-406071.htmlreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2023-02-14T15:23:15Zoai:repositorio.unifesp.br/:11600/30616Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652023-02-14T15:23:15Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Methacholine vs adenosine on intra and extrathoracic airway hyperresponsiveness in patients with cough variant asthma |
title |
Methacholine vs adenosine on intra and extrathoracic airway hyperresponsiveness in patients with cough variant asthma |
spellingShingle |
Methacholine vs adenosine on intra and extrathoracic airway hyperresponsiveness in patients with cough variant asthma Ribeiro, M. [UNIFESP] |
title_short |
Methacholine vs adenosine on intra and extrathoracic airway hyperresponsiveness in patients with cough variant asthma |
title_full |
Methacholine vs adenosine on intra and extrathoracic airway hyperresponsiveness in patients with cough variant asthma |
title_fullStr |
Methacholine vs adenosine on intra and extrathoracic airway hyperresponsiveness in patients with cough variant asthma |
title_full_unstemmed |
Methacholine vs adenosine on intra and extrathoracic airway hyperresponsiveness in patients with cough variant asthma |
title_sort |
Methacholine vs adenosine on intra and extrathoracic airway hyperresponsiveness in patients with cough variant asthma |
author |
Ribeiro, M. [UNIFESP] |
author_facet |
Ribeiro, M. [UNIFESP] Pereira, C. A. C. [UNIFESP] Nery, L. E. [UNIFESP] Beppu, O. S. [UNIFESP] Silva, C. O. S. [UNIFESP] |
author_role |
author |
author2 |
Pereira, C. A. C. [UNIFESP] Nery, L. E. [UNIFESP] Beppu, O. S. [UNIFESP] Silva, C. O. S. [UNIFESP] |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Ribeiro, M. [UNIFESP] Pereira, C. A. C. [UNIFESP] Nery, L. E. [UNIFESP] Beppu, O. S. [UNIFESP] Silva, C. O. S. [UNIFESP] |
description |
Background: Airway hyperresponsiveness (AHR) can be studied by bronchoprovocation test (BPT) using direct (methacholine - MCh) or indirect (adenosine 5'-monophosphate - AMP) stimuli. These two substances have not been compared in cough variant asthma (CVA).Objective: We designed a randomized, single-blind, cross-over study to compare AMP and MCh in the detection of CVA. Additionally, we examined whether assessment of extrathoracic airway hyperresponsiveness (EAHR) during MCh and AMP helped in the evaluation of CVA.Methods: Patients with CVA with previous positive MCh BPT performed challenges with AMP and MCh. the variables were: (i) a provocative dose producing a 20% fall in forced expiratory volume in 1 s (FEV(1)) value (PD(20)MCh); (ii) a provocative dose producing a 25% fall in the maximal mid-inspiratory flow (FIF(50)) from baseline (PD(25)MCh) for MCh; (iii) a provocative concentration producing a 20% fall in FEV(1) value (PC(20)AMP) and (iv) a provocative concentration producing a 25% fall in the FIF(50) from baseline (PC(25)AMP) for AMP.Results: All 113 patients with CVA responded to PD(20)MCh and 96% and 69% responded to PC(20)AMP, if we used PC(20) <= 200 mg/ml or PC(20) <= 100 mg/ml, respectively, with an excellent correlation between these two tests (r = 0.87 and 0.76, respectively). Extrathoracic AHR associated with AHR was found in 10% in MCh challenge and in 11% with AMP challenge and no patients had EAHR alone.Conclusion: Adenosine challenges correlate well with MCh in patients with CVA. A minority (c. 10%) of CVA patients have EAHR as measured by these tests, while most had AHR as assessed with each of the challenge agents. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-05-01 2016-01-24T13:49:46Z 2016-01-24T13:49:46Z |
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/10.1111/j.1398-9995.2007.01589.x Allergy. Malden: Wiley-Blackwell Publishing, Inc, v. 63, n. 5, p. 527-532, 2008. 10.1111/j.1398-9995.2007.01589.x 0105-4538 http://repositorio.unifesp.br/handle/11600/30616 WOS:000254638700006 |
url |
http://dx.doi.org/10.1111/j.1398-9995.2007.01589.x http://repositorio.unifesp.br/handle/11600/30616 |
identifier_str_mv |
Allergy. Malden: Wiley-Blackwell Publishing, Inc, v. 63, n. 5, p. 527-532, 2008. 10.1111/j.1398-9995.2007.01589.x 0105-4538 WOS:000254638700006 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Allergy |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess http://olabout.wiley.com/WileyCDA/Section/id-406071.html |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://olabout.wiley.com/WileyCDA/Section/id-406071.html |
dc.format.none.fl_str_mv |
527-532 |
dc.publisher.none.fl_str_mv |
Wiley-Blackwell |
publisher.none.fl_str_mv |
Wiley-Blackwell |
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 |
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Repositório Institucional da UNIFESP |
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Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
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biblioteca.csp@unifesp.br |
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