Targeting the small airways with dry powder adenosine: a challenging concept
Background: Small-particle inhaled corticosteroids (ICS) provide a higher small airway deposition than large-particle ICS. However, we are still not able to identify asthma patients who will profit most from small-particle treatment. Objective: We aimed to identify these patients by selectively chal...
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creator | van der Wiel, Erica Lexmond, Anne J. van den Berge, Maarten Postma, Dirkje S. Hagedoorn, Paul Frijlink, Henderik W. Farenhorst, Martijn P. de Boer, Anne H. ten Hacken, Nick H. T. |
description | Background: Small-particle inhaled corticosteroids (ICS) provide a higher small airway deposition than large-particle ICS. However, we are still not able to identify asthma patients who will profit most from small-particle treatment.
Objective: We aimed to identify these patients by selectively challenging the small and large airways. We hypothesized that the airways could be challenged selectively using small- and large-particle adenosine, both inhaled at a high and a low flow rate.
Design: In this cross-over study 11 asthma subjects performed four dry powder adenosine tests, with either small (MMAD 2.7 µm) or large (MMAD 6.0 µm) particles, inhaled once with a low flow rate (30 l min
-1
) and once with a high flow rate (60 l min
-1
). Spirometry and impulse oscillometry were performed after every bronchoprovocation step. We assumed that FEV
1
reflects the large airways, and FEF
25-75%
, R5-R20 and X5 reflect the small airways.
Results: The four adenosine tests were not significantly different with respect to the threshold values of FEV
1
(p = 0.12), FEF
25-75%
(p = 0.37), R5-R20 (p = 0.60) or X5 (p = 0.46). Both small- and large-particle adenosine induced a response in the small airways in the majority of the tests.
Conclusions: In contrast to our hypothesis, all four adenosine tests provoked a response in the small airways and we could not identify different large- or small-airway responders. Interestingly, even the test with large particles and a high flow rate induced a small-airway response, suggesting that selective challenging of the small airways is not necessary. Future studies should investigate the relation between particle deposition and the site of an airway response. |
doi_str_mv | 10.1080/20018525.2017.1369328 |
format | Article |
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Objective: We aimed to identify these patients by selectively challenging the small and large airways. We hypothesized that the airways could be challenged selectively using small- and large-particle adenosine, both inhaled at a high and a low flow rate.
Design: In this cross-over study 11 asthma subjects performed four dry powder adenosine tests, with either small (MMAD 2.7 µm) or large (MMAD 6.0 µm) particles, inhaled once with a low flow rate (30 l min
-1
) and once with a high flow rate (60 l min
-1
). Spirometry and impulse oscillometry were performed after every bronchoprovocation step. We assumed that FEV
1
reflects the large airways, and FEF
25-75%
, R5-R20 and X5 reflect the small airways.
Results: The four adenosine tests were not significantly different with respect to the threshold values of FEV
1
(p = 0.12), FEF
25-75%
(p = 0.37), R5-R20 (p = 0.60) or X5 (p = 0.46). Both small- and large-particle adenosine induced a response in the small airways in the majority of the tests.
Conclusions: In contrast to our hypothesis, all four adenosine tests provoked a response in the small airways and we could not identify different large- or small-airway responders. Interestingly, even the test with large particles and a high flow rate induced a small-airway response, suggesting that selective challenging of the small airways is not necessary. Future studies should investigate the relation between particle deposition and the site of an airway response.</description><identifier>ISSN: 2001-8525</identifier><identifier>EISSN: 2001-8525</identifier><identifier>DOI: 10.1080/20018525.2017.1369328</identifier><identifier>PMID: 29057065</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Adenosine ; Asthma ; bronchial hyperresponsiveness ; bronchoprovocation test ; Original ; small airways</subject><ispartof>European clinical respiratory journal, 2017, Vol.4 (1), p.1369328-1369328</ispartof><rights>2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2017</rights><rights>2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This work is licensed under the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2017 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c562t-782a75eae7596d4d73a3714bf55177bb3002228016aa82c774f1e8db90c6aaa3</citedby><cites>FETCH-LOGICAL-c562t-782a75eae7596d4d73a3714bf55177bb3002228016aa82c774f1e8db90c6aaa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642194/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642194/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,4010,27479,27900,27901,27902,53766,53768,59116,59117</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29057065$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van der Wiel, Erica</creatorcontrib><creatorcontrib>Lexmond, Anne J.</creatorcontrib><creatorcontrib>van den Berge, Maarten</creatorcontrib><creatorcontrib>Postma, Dirkje S.</creatorcontrib><creatorcontrib>Hagedoorn, Paul</creatorcontrib><creatorcontrib>Frijlink, Henderik W.</creatorcontrib><creatorcontrib>Farenhorst, Martijn P.</creatorcontrib><creatorcontrib>de Boer, Anne H.</creatorcontrib><creatorcontrib>ten Hacken, Nick H. T.</creatorcontrib><title>Targeting the small airways with dry powder adenosine: a challenging concept</title><title>European clinical respiratory journal</title><addtitle>Eur Clin Respir J</addtitle><description>Background: Small-particle inhaled corticosteroids (ICS) provide a higher small airway deposition than large-particle ICS. However, we are still not able to identify asthma patients who will profit most from small-particle treatment.
Objective: We aimed to identify these patients by selectively challenging the small and large airways. We hypothesized that the airways could be challenged selectively using small- and large-particle adenosine, both inhaled at a high and a low flow rate.
Design: In this cross-over study 11 asthma subjects performed four dry powder adenosine tests, with either small (MMAD 2.7 µm) or large (MMAD 6.0 µm) particles, inhaled once with a low flow rate (30 l min
-1
) and once with a high flow rate (60 l min
-1
). Spirometry and impulse oscillometry were performed after every bronchoprovocation step. We assumed that FEV
1
reflects the large airways, and FEF
25-75%
, R5-R20 and X5 reflect the small airways.
Results: The four adenosine tests were not significantly different with respect to the threshold values of FEV
1
(p = 0.12), FEF
25-75%
(p = 0.37), R5-R20 (p = 0.60) or X5 (p = 0.46). Both small- and large-particle adenosine induced a response in the small airways in the majority of the tests.
Conclusions: In contrast to our hypothesis, all four adenosine tests provoked a response in the small airways and we could not identify different large- or small-airway responders. Interestingly, even the test with large particles and a high flow rate induced a small-airway response, suggesting that selective challenging of the small airways is not necessary. Future studies should investigate the relation between particle deposition and the site of an airway response.</description><subject>Adenosine</subject><subject>Asthma</subject><subject>bronchial hyperresponsiveness</subject><subject>bronchoprovocation test</subject><subject>Original</subject><subject>small airways</subject><issn>2001-8525</issn><issn>2001-8525</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><sourceid>DOA</sourceid><recordid>eNp9kUFvGyEQhVdVqyZK8xNardRLL3aBhQV6qBpFbRLJUi--o1lg11gsuLCu5X9ftnaipIeegDffvAFeVb3HaImRQJ8JQlgwwpYEYb7ETSsbIl5Vl7O-mAuvn-0vquuct6gcmaQCsbfVBZGIcdSyy2q1hjTYyYWhnja2ziN4X4NLBzjm-uCmTW3Ssd7Fg7GpBmNDzC7YLzXUelNQG4a5Vceg7W56V73pwWd7fV6vqvWP7-vb-8Xq593D7c1qoVlLpgUXBDizYDmTraGGN9BwTLueMcx51zUIEUIEwi2AIJpz2mMrTCeRLgo0V9XDydZE2KpdciOko4rg1F8hpkFBmpz2VnUNh44IzATuqOl6IIIDEpRaYpjoefH6evLa7bvRGm3DlMC_MH1ZCW6jhvhbsZYSLGkx-HQ2SPHX3uZJjS5r6z0EG_dZYcloIyljoqAf_0G3cZ9C-SlFaMukRFzIQrETpVPMOdn-6TIYqTl99Zi-mtNX5_RL34fnL3nqesy6AN9OgAt9TCMcYvJGTXD0MfUJgnZZNf-f8QemgL2r</recordid><startdate>2017</startdate><enddate>2017</enddate><creator>van der Wiel, Erica</creator><creator>Lexmond, Anne J.</creator><creator>van den Berge, Maarten</creator><creator>Postma, Dirkje S.</creator><creator>Hagedoorn, Paul</creator><creator>Frijlink, Henderik W.</creator><creator>Farenhorst, Martijn P.</creator><creator>de Boer, Anne H.</creator><creator>ten Hacken, Nick H. T.</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><general>Taylor & Francis Group</general><scope>0YH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>2017</creationdate><title>Targeting the small airways with dry powder adenosine: a challenging concept</title><author>van der Wiel, Erica ; Lexmond, Anne J. ; van den Berge, Maarten ; Postma, Dirkje S. ; Hagedoorn, Paul ; Frijlink, Henderik W. ; Farenhorst, Martijn P. ; de Boer, Anne H. ; ten Hacken, Nick H. T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c562t-782a75eae7596d4d73a3714bf55177bb3002228016aa82c774f1e8db90c6aaa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adenosine</topic><topic>Asthma</topic><topic>bronchial hyperresponsiveness</topic><topic>bronchoprovocation test</topic><topic>Original</topic><topic>small airways</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van der Wiel, Erica</creatorcontrib><creatorcontrib>Lexmond, Anne J.</creatorcontrib><creatorcontrib>van den Berge, Maarten</creatorcontrib><creatorcontrib>Postma, Dirkje S.</creatorcontrib><creatorcontrib>Hagedoorn, Paul</creatorcontrib><creatorcontrib>Frijlink, Henderik W.</creatorcontrib><creatorcontrib>Farenhorst, Martijn P.</creatorcontrib><creatorcontrib>de Boer, Anne H.</creatorcontrib><creatorcontrib>ten Hacken, Nick H. T.</creatorcontrib><collection>Taylor & Francis Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>European clinical respiratory journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van der Wiel, Erica</au><au>Lexmond, Anne J.</au><au>van den Berge, Maarten</au><au>Postma, Dirkje S.</au><au>Hagedoorn, Paul</au><au>Frijlink, Henderik W.</au><au>Farenhorst, Martijn P.</au><au>de Boer, Anne H.</au><au>ten Hacken, Nick H. T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeting the small airways with dry powder adenosine: a challenging concept</atitle><jtitle>European clinical respiratory journal</jtitle><addtitle>Eur Clin Respir J</addtitle><date>2017</date><risdate>2017</risdate><volume>4</volume><issue>1</issue><spage>1369328</spage><epage>1369328</epage><pages>1369328-1369328</pages><issn>2001-8525</issn><eissn>2001-8525</eissn><abstract>Background: Small-particle inhaled corticosteroids (ICS) provide a higher small airway deposition than large-particle ICS. However, we are still not able to identify asthma patients who will profit most from small-particle treatment.
Objective: We aimed to identify these patients by selectively challenging the small and large airways. We hypothesized that the airways could be challenged selectively using small- and large-particle adenosine, both inhaled at a high and a low flow rate.
Design: In this cross-over study 11 asthma subjects performed four dry powder adenosine tests, with either small (MMAD 2.7 µm) or large (MMAD 6.0 µm) particles, inhaled once with a low flow rate (30 l min
-1
) and once with a high flow rate (60 l min
-1
). Spirometry and impulse oscillometry were performed after every bronchoprovocation step. We assumed that FEV
1
reflects the large airways, and FEF
25-75%
, R5-R20 and X5 reflect the small airways.
Results: The four adenosine tests were not significantly different with respect to the threshold values of FEV
1
(p = 0.12), FEF
25-75%
(p = 0.37), R5-R20 (p = 0.60) or X5 (p = 0.46). Both small- and large-particle adenosine induced a response in the small airways in the majority of the tests.
Conclusions: In contrast to our hypothesis, all four adenosine tests provoked a response in the small airways and we could not identify different large- or small-airway responders. Interestingly, even the test with large particles and a high flow rate induced a small-airway response, suggesting that selective challenging of the small airways is not necessary. Future studies should investigate the relation between particle deposition and the site of an airway response.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>29057065</pmid><doi>10.1080/20018525.2017.1369328</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Asthma bronchial hyperresponsiveness bronchoprovocation test Original small airways |
title | Targeting the small airways with dry powder adenosine: a challenging concept |
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