Randomized controlled trial of triple versus dual inhaler therapy on small airways in smoking asthmatics
Background Smoking worsens underlying asthma inflammation and also induces resistance to inhaled corticosteroids (ICS). Small airways dysfunction measured by impulse oscillometry (IOS) is associated with worse control. Objectives We investigated the effects on small airways of adding long‐acting bet...
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Veröffentlicht in: | Clinical and experimental allergy 2020-10, Vol.50 (10), p.1140-1147 |
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description | Background
Smoking worsens underlying asthma inflammation and also induces resistance to inhaled corticosteroids (ICS). Small airways dysfunction measured by impulse oscillometry (IOS) is associated with worse control.
Objectives
We investigated the effects on small airways of adding long‐acting beta‐agonist (LABA) alone or with long‐acting muscarinic antagonist (LAMA) to ICS in asthmatic smokers.
Methods
Sixteen current smokers were enrolled: mean age 44 year, FEV1 84%, FEF25‐75 47%, R5 158%, ACQ 1.69, 20 pack year . Patients were converted to a reference ICS as HFA‐BDP during initial run‐in at median dose of 800 µg/day. Open label olodaterol 5 µg od (OLO) or olodaterol 5 µg/tiotropium 5 µg od (OLO/TIO) was added to HFA‐BDP for median duration of 3 weeks in a randomized cross over design, including run‐in and washout periods on HFA‐BDP. IOS and spirometry were measured after each treatment (BDP/OLO/TIO or BDP/OLO) and at baseline after run‐in and washout (BDP).
Results
After chronic dosing, IOS outcomes at trough except for R20 were all significantly improved with OLO/TIO compared to OLO. For the primary end‐point of total airway resistance (as R5), the mean difference (95%CI) at trough was 0.06 (0.015‐0.10) kPa/l/s, peripheral airways resistance (as R5‐R20) 0.03 (0.003‐0.06) kPa/l/s, peripheral lung reactance area (as AX) 0.38 (0.08‐0.68) kPa/l and resonant frequency (as RF) 2.28 (0.45‐4.12) Hz. FEF25‐75 at trough was also better with OLO/TIO vs TIO: 0.93 (0.86 ‐ 0.95) l/s while FEV1 was not different.
Conclusions
ICS/LABA/LAMA was superior to ICS/LABA on trough small airway outcomes in asthma patients who smoke. |
doi_str_mv | 10.1111/cea.13702 |
format | Article |
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Smoking worsens underlying asthma inflammation and also induces resistance to inhaled corticosteroids (ICS). Small airways dysfunction measured by impulse oscillometry (IOS) is associated with worse control.
Objectives
We investigated the effects on small airways of adding long‐acting beta‐agonist (LABA) alone or with long‐acting muscarinic antagonist (LAMA) to ICS in asthmatic smokers.
Methods
Sixteen current smokers were enrolled: mean age 44 year, FEV1 84%, FEF25‐75 47%, R5 158%, ACQ 1.69, 20 pack year . Patients were converted to a reference ICS as HFA‐BDP during initial run‐in at median dose of 800 µg/day. Open label olodaterol 5 µg od (OLO) or olodaterol 5 µg/tiotropium 5 µg od (OLO/TIO) was added to HFA‐BDP for median duration of 3 weeks in a randomized cross over design, including run‐in and washout periods on HFA‐BDP. IOS and spirometry were measured after each treatment (BDP/OLO/TIO or BDP/OLO) and at baseline after run‐in and washout (BDP).
Results
After chronic dosing, IOS outcomes at trough except for R20 were all significantly improved with OLO/TIO compared to OLO. For the primary end‐point of total airway resistance (as R5), the mean difference (95%CI) at trough was 0.06 (0.015‐0.10) kPa/l/s, peripheral airways resistance (as R5‐R20) 0.03 (0.003‐0.06) kPa/l/s, peripheral lung reactance area (as AX) 0.38 (0.08‐0.68) kPa/l and resonant frequency (as RF) 2.28 (0.45‐4.12) Hz. FEF25‐75 at trough was also better with OLO/TIO vs TIO: 0.93 (0.86 ‐ 0.95) l/s while FEV1 was not different.
Conclusions
ICS/LABA/LAMA was superior to ICS/LABA on trough small airway outcomes in asthma patients who smoke.</description><identifier>ISSN: 0954-7894</identifier><identifier>EISSN: 1365-2222</identifier><identifier>DOI: 10.1111/cea.13702</identifier><identifier>PMID: 33180376</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Acetylcholine receptors (muscarinic) ; Asthma ; Corticosteroids ; Dosage ; Inhalers ; pneumology ; quality of life ; Respiratory tract ; small airways ; Smoking ; triple therapy</subject><ispartof>Clinical and experimental allergy, 2020-10, Vol.50 (10), p.1140-1147</ispartof><rights>2020 The Authors. published by John Wiley & Sons Ltd</rights><rights>2020 The Authors. Clinical & Experimental Allergy published by John Wiley & Sons Ltd.</rights><rights>Copyright Wiley Subscription Services, Inc. Oct 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3882-9134487b2059e84f3603d4576aad4852342f5b85d41d009e75e3131ac0af26dd3</citedby><cites>FETCH-LOGICAL-c3882-9134487b2059e84f3603d4576aad4852342f5b85d41d009e75e3131ac0af26dd3</cites><orcidid>0000-0002-8140-2014 ; 0000-0002-9604-9807 ; 0000-0001-5954-6620</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fcea.13702$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fcea.13702$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33180376$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jabbal, Sunny</creatorcontrib><creatorcontrib>Kuo, Chris RuiWen</creatorcontrib><creatorcontrib>Lipworth, Brian</creatorcontrib><title>Randomized controlled trial of triple versus dual inhaler therapy on small airways in smoking asthmatics</title><title>Clinical and experimental allergy</title><addtitle>Clin Exp Allergy</addtitle><description>Background
Smoking worsens underlying asthma inflammation and also induces resistance to inhaled corticosteroids (ICS). Small airways dysfunction measured by impulse oscillometry (IOS) is associated with worse control.
Objectives
We investigated the effects on small airways of adding long‐acting beta‐agonist (LABA) alone or with long‐acting muscarinic antagonist (LAMA) to ICS in asthmatic smokers.
Methods
Sixteen current smokers were enrolled: mean age 44 year, FEV1 84%, FEF25‐75 47%, R5 158%, ACQ 1.69, 20 pack year . Patients were converted to a reference ICS as HFA‐BDP during initial run‐in at median dose of 800 µg/day. Open label olodaterol 5 µg od (OLO) or olodaterol 5 µg/tiotropium 5 µg od (OLO/TIO) was added to HFA‐BDP for median duration of 3 weeks in a randomized cross over design, including run‐in and washout periods on HFA‐BDP. IOS and spirometry were measured after each treatment (BDP/OLO/TIO or BDP/OLO) and at baseline after run‐in and washout (BDP).
Results
After chronic dosing, IOS outcomes at trough except for R20 were all significantly improved with OLO/TIO compared to OLO. For the primary end‐point of total airway resistance (as R5), the mean difference (95%CI) at trough was 0.06 (0.015‐0.10) kPa/l/s, peripheral airways resistance (as R5‐R20) 0.03 (0.003‐0.06) kPa/l/s, peripheral lung reactance area (as AX) 0.38 (0.08‐0.68) kPa/l and resonant frequency (as RF) 2.28 (0.45‐4.12) Hz. FEF25‐75 at trough was also better with OLO/TIO vs TIO: 0.93 (0.86 ‐ 0.95) l/s while FEV1 was not different.
Conclusions
ICS/LABA/LAMA was superior to ICS/LABA on trough small airway outcomes in asthma patients who smoke.</description><subject>Acetylcholine receptors (muscarinic)</subject><subject>Asthma</subject><subject>Corticosteroids</subject><subject>Dosage</subject><subject>Inhalers</subject><subject>pneumology</subject><subject>quality of life</subject><subject>Respiratory tract</subject><subject>small airways</subject><subject>Smoking</subject><subject>triple therapy</subject><issn>0954-7894</issn><issn>1365-2222</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNp10E1LxDAQBuAgiq4fB_-ABLzooTppkjY9yuIXCILoucw2qRtNmzVplfXXG131IDiXDMPDS3gJ2WdwwtKcNgZPGC8hXyMTxguZ5WnWyQQqKbJSVWKLbMf4BABcVmqTbHHOFPCymJD5Hfbad_bdaNr4fgjeubQOwaKjvv1cFs7QVxPiGKke09X2c3Qm0GFuAi6W1Pc0dugcRRvecBkTSAf_bPtHinGYdzjYJu6SjRZdNHvf7w55uDi_n15lN7eX19Ozm6zhSuVZxbgQqpzlICujRMsL4FrIskDUQsmci7yVMyW1YBqgMqU0nHGGDWCbF1rzHXK0yl0E_zKaONSdjY1xDnvjx1jnogBQjFeQ6OEf-uTH0KffJSXKsigqkEkdr1QTfIzBtPUi2A7DsmZQf9Zfp_rrr_qTPfhOHGed0b_yp-8ETlfgzTqz_D-pnp6frSI_ANGYjfg</recordid><startdate>202010</startdate><enddate>202010</enddate><creator>Jabbal, Sunny</creator><creator>Kuo, Chris RuiWen</creator><creator>Lipworth, Brian</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8140-2014</orcidid><orcidid>https://orcid.org/0000-0002-9604-9807</orcidid><orcidid>https://orcid.org/0000-0001-5954-6620</orcidid></search><sort><creationdate>202010</creationdate><title>Randomized controlled trial of triple versus dual inhaler therapy on small airways in smoking asthmatics</title><author>Jabbal, Sunny ; Kuo, Chris RuiWen ; Lipworth, Brian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3882-9134487b2059e84f3603d4576aad4852342f5b85d41d009e75e3131ac0af26dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acetylcholine receptors (muscarinic)</topic><topic>Asthma</topic><topic>Corticosteroids</topic><topic>Dosage</topic><topic>Inhalers</topic><topic>pneumology</topic><topic>quality of life</topic><topic>Respiratory tract</topic><topic>small airways</topic><topic>Smoking</topic><topic>triple therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jabbal, Sunny</creatorcontrib><creatorcontrib>Kuo, Chris RuiWen</creatorcontrib><creatorcontrib>Lipworth, Brian</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and experimental allergy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jabbal, Sunny</au><au>Kuo, Chris RuiWen</au><au>Lipworth, Brian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Randomized controlled trial of triple versus dual inhaler therapy on small airways in smoking asthmatics</atitle><jtitle>Clinical and experimental allergy</jtitle><addtitle>Clin Exp Allergy</addtitle><date>2020-10</date><risdate>2020</risdate><volume>50</volume><issue>10</issue><spage>1140</spage><epage>1147</epage><pages>1140-1147</pages><issn>0954-7894</issn><eissn>1365-2222</eissn><abstract>Background
Smoking worsens underlying asthma inflammation and also induces resistance to inhaled corticosteroids (ICS). Small airways dysfunction measured by impulse oscillometry (IOS) is associated with worse control.
Objectives
We investigated the effects on small airways of adding long‐acting beta‐agonist (LABA) alone or with long‐acting muscarinic antagonist (LAMA) to ICS in asthmatic smokers.
Methods
Sixteen current smokers were enrolled: mean age 44 year, FEV1 84%, FEF25‐75 47%, R5 158%, ACQ 1.69, 20 pack year . Patients were converted to a reference ICS as HFA‐BDP during initial run‐in at median dose of 800 µg/day. Open label olodaterol 5 µg od (OLO) or olodaterol 5 µg/tiotropium 5 µg od (OLO/TIO) was added to HFA‐BDP for median duration of 3 weeks in a randomized cross over design, including run‐in and washout periods on HFA‐BDP. IOS and spirometry were measured after each treatment (BDP/OLO/TIO or BDP/OLO) and at baseline after run‐in and washout (BDP).
Results
After chronic dosing, IOS outcomes at trough except for R20 were all significantly improved with OLO/TIO compared to OLO. For the primary end‐point of total airway resistance (as R5), the mean difference (95%CI) at trough was 0.06 (0.015‐0.10) kPa/l/s, peripheral airways resistance (as R5‐R20) 0.03 (0.003‐0.06) kPa/l/s, peripheral lung reactance area (as AX) 0.38 (0.08‐0.68) kPa/l and resonant frequency (as RF) 2.28 (0.45‐4.12) Hz. FEF25‐75 at trough was also better with OLO/TIO vs TIO: 0.93 (0.86 ‐ 0.95) l/s while FEV1 was not different.
Conclusions
ICS/LABA/LAMA was superior to ICS/LABA on trough small airway outcomes in asthma patients who smoke.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33180376</pmid><doi>10.1111/cea.13702</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-8140-2014</orcidid><orcidid>https://orcid.org/0000-0002-9604-9807</orcidid><orcidid>https://orcid.org/0000-0001-5954-6620</orcidid><oa>free_for_read</oa></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete |
subjects | Acetylcholine receptors (muscarinic) Asthma Corticosteroids Dosage Inhalers pneumology quality of life Respiratory tract small airways Smoking triple therapy |
title | Randomized controlled trial of triple versus dual inhaler therapy on small airways in smoking asthmatics |
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