Exhaled nitric oxide levels in patients with atopic cough and cough variant asthma

Background and objective:  Atopic cough (AC) is an established clinical entity in Japan, in which patients present with a chronic persistent non‐productive cough. Exhaled nitric oxide (NO) is a biomarker of eosinophilic airway inflammation. The present study examined whether exhaled NO levels were i...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Respirology (Carlton, Vic.) Vic.), 2008-05, Vol.13 (3), p.359-364
Hauptverfasser: FUJIMURA, Masaki, OHKURA, Noriyuki, ABO, Miki, FURUSHO, Shiho, WASEDA, Yuko, ICHIKAWA, Yukari, HARA, Johsuke
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 364
container_issue 3
container_start_page 359
container_title Respirology (Carlton, Vic.)
container_volume 13
creator FUJIMURA, Masaki
OHKURA, Noriyuki
ABO, Miki
FURUSHO, Shiho
WASEDA, Yuko
ICHIKAWA, Yukari
HARA, Johsuke
description Background and objective:  Atopic cough (AC) is an established clinical entity in Japan, in which patients present with a chronic persistent non‐productive cough. Exhaled nitric oxide (NO) is a biomarker of eosinophilic airway inflammation. The present study examined whether exhaled NO levels were increased in AC in comparison with cough variant asthma (CVA) and bronchial asthma (BA). Methods:  Consecutive patients presenting with an isolated cough lasting at least 8 weeks were enrolled in the study. The aetiology of the chronic cough was determined according to the Japanese Respiratory Society guidelines for management of cough. Exhaled NO, capsaicin cough sensitivity (capsaicin concentration eliciting five or more coughs (C5)) and bronchial reversibility were measured at the patients’ first visit. Bronchial responsiveness (PC20 to methacholine) was measured at their second visit following a 6‐day course of bronchodilator therapy. Results:  There were 58 patients recruited and fully investigated; of these 9 and 11 patients were diagnosed with AC and CVA, respectively, as single causes of chronic cough. Ten patients with BA who had not received corticosteroid therapy in the previous 4 weeks and who attended the same clinic in the same time period acted as controls. Exhaled NO levels in patients with AC were significantly lower than those in patients with CVA and BA. There was no significant difference in the exhaled NO levels between patients with CVA and BA. Conclusions:  Exhaled NO may reflect eosinophilic inflammation of peripheral airways and its measurement may be useful in differentiating CVA from AC and other causes of chronic non‐productive cough.
doi_str_mv 10.1111/j.1440-1843.2008.01273.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70486941</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70486941</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5263-40dea486df0ccf74a2f47f28b02726dad93625774f3d36d80d7a9829a4e749f03</originalsourceid><addsrcrecordid>eNqNkEFPwyAYhonROJ3-BcPJWysFWuBiYpY5TYwum8YjwUIds2tnYbP791K76FUuvIT3e77kAQAmKE7CuVrGCaUoSjglMUaIxyjBjMTtATj5_TgMmWASMSbEAJw6t0QIkRSlx2CQcCIET9kJmI3bhSqNhpX1jc1h3VptYGm2pnTQVnCtvDWVd_DL-gVUvl6HUl5v3sOj0vu0VY1VlYfK-cVKnYGjQpXOnO_vIXi5HT-P7qKHp8n96OYhylOckYgibRTlmS5QnheMKlxQVmD-hjDDmVZakAynjNGCaJJpjjRTgmOhqGFUFIgMwWXPXTf158Y4L1fW5aYsVWXqjZMMBbqgSSjyvpg3tXONKeS6sSvV7GSCZOdTLmWnTXbaZOdT_viUbRi92O_YvK2M_hvcCwyF677wZUuz-zdYzsbzaRcDIOoB1nnT_gJU8yEzRlgqXx8nUsxHk9l8SiQl316yk04</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70486941</pqid></control><display><type>article</type><title>Exhaled nitric oxide levels in patients with atopic cough and cough variant asthma</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>FUJIMURA, Masaki ; OHKURA, Noriyuki ; ABO, Miki ; FURUSHO, Shiho ; WASEDA, Yuko ; ICHIKAWA, Yukari ; HARA, Johsuke</creator><creatorcontrib>FUJIMURA, Masaki ; OHKURA, Noriyuki ; ABO, Miki ; FURUSHO, Shiho ; WASEDA, Yuko ; ICHIKAWA, Yukari ; HARA, Johsuke</creatorcontrib><description>Background and objective:  Atopic cough (AC) is an established clinical entity in Japan, in which patients present with a chronic persistent non‐productive cough. Exhaled nitric oxide (NO) is a biomarker of eosinophilic airway inflammation. The present study examined whether exhaled NO levels were increased in AC in comparison with cough variant asthma (CVA) and bronchial asthma (BA). Methods:  Consecutive patients presenting with an isolated cough lasting at least 8 weeks were enrolled in the study. The aetiology of the chronic cough was determined according to the Japanese Respiratory Society guidelines for management of cough. Exhaled NO, capsaicin cough sensitivity (capsaicin concentration eliciting five or more coughs (C5)) and bronchial reversibility were measured at the patients’ first visit. Bronchial responsiveness (PC20 to methacholine) was measured at their second visit following a 6‐day course of bronchodilator therapy. Results:  There were 58 patients recruited and fully investigated; of these 9 and 11 patients were diagnosed with AC and CVA, respectively, as single causes of chronic cough. Ten patients with BA who had not received corticosteroid therapy in the previous 4 weeks and who attended the same clinic in the same time period acted as controls. Exhaled NO levels in patients with AC were significantly lower than those in patients with CVA and BA. There was no significant difference in the exhaled NO levels between patients with CVA and BA. Conclusions:  Exhaled NO may reflect eosinophilic inflammation of peripheral airways and its measurement may be useful in differentiating CVA from AC and other causes of chronic non‐productive cough.</description><identifier>ISSN: 1323-7799</identifier><identifier>EISSN: 1440-1843</identifier><identifier>DOI: 10.1111/j.1440-1843.2008.01273.x</identifier><identifier>PMID: 18399857</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Publishing Asia</publisher><subject>Adult ; Asthma - diagnosis ; Asthma - drug therapy ; Asthma - metabolism ; atopic cough ; Biomarkers - metabolism ; Breath Tests ; bronchial asthma ; Bronchial Provocation Tests ; Bronchodilator Agents - therapeutic use ; Case-Control Studies ; Cough - diagnosis ; Cough - drug therapy ; Cough - metabolism ; cough variant asthma ; Cross-Sectional Studies ; Diagnosis, Differential ; exhaled nitric oxide ; Female ; Humans ; Male ; Middle Aged ; Nitric Oxide - metabolism ; non-asthmatic eosinophilic bronchitis ; Pneumonia - metabolism ; Respiratory Function Tests</subject><ispartof>Respirology (Carlton, Vic.), 2008-05, Vol.13 (3), p.359-364</ispartof><rights>2008 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5263-40dea486df0ccf74a2f47f28b02726dad93625774f3d36d80d7a9829a4e749f03</citedby><cites>FETCH-LOGICAL-c5263-40dea486df0ccf74a2f47f28b02726dad93625774f3d36d80d7a9829a4e749f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1440-1843.2008.01273.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1440-1843.2008.01273.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18399857$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FUJIMURA, Masaki</creatorcontrib><creatorcontrib>OHKURA, Noriyuki</creatorcontrib><creatorcontrib>ABO, Miki</creatorcontrib><creatorcontrib>FURUSHO, Shiho</creatorcontrib><creatorcontrib>WASEDA, Yuko</creatorcontrib><creatorcontrib>ICHIKAWA, Yukari</creatorcontrib><creatorcontrib>HARA, Johsuke</creatorcontrib><title>Exhaled nitric oxide levels in patients with atopic cough and cough variant asthma</title><title>Respirology (Carlton, Vic.)</title><addtitle>Respirology</addtitle><description>Background and objective:  Atopic cough (AC) is an established clinical entity in Japan, in which patients present with a chronic persistent non‐productive cough. Exhaled nitric oxide (NO) is a biomarker of eosinophilic airway inflammation. The present study examined whether exhaled NO levels were increased in AC in comparison with cough variant asthma (CVA) and bronchial asthma (BA). Methods:  Consecutive patients presenting with an isolated cough lasting at least 8 weeks were enrolled in the study. The aetiology of the chronic cough was determined according to the Japanese Respiratory Society guidelines for management of cough. Exhaled NO, capsaicin cough sensitivity (capsaicin concentration eliciting five or more coughs (C5)) and bronchial reversibility were measured at the patients’ first visit. Bronchial responsiveness (PC20 to methacholine) was measured at their second visit following a 6‐day course of bronchodilator therapy. Results:  There were 58 patients recruited and fully investigated; of these 9 and 11 patients were diagnosed with AC and CVA, respectively, as single causes of chronic cough. Ten patients with BA who had not received corticosteroid therapy in the previous 4 weeks and who attended the same clinic in the same time period acted as controls. Exhaled NO levels in patients with AC were significantly lower than those in patients with CVA and BA. There was no significant difference in the exhaled NO levels between patients with CVA and BA. Conclusions:  Exhaled NO may reflect eosinophilic inflammation of peripheral airways and its measurement may be useful in differentiating CVA from AC and other causes of chronic non‐productive cough.</description><subject>Adult</subject><subject>Asthma - diagnosis</subject><subject>Asthma - drug therapy</subject><subject>Asthma - metabolism</subject><subject>atopic cough</subject><subject>Biomarkers - metabolism</subject><subject>Breath Tests</subject><subject>bronchial asthma</subject><subject>Bronchial Provocation Tests</subject><subject>Bronchodilator Agents - therapeutic use</subject><subject>Case-Control Studies</subject><subject>Cough - diagnosis</subject><subject>Cough - drug therapy</subject><subject>Cough - metabolism</subject><subject>cough variant asthma</subject><subject>Cross-Sectional Studies</subject><subject>Diagnosis, Differential</subject><subject>exhaled nitric oxide</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nitric Oxide - metabolism</subject><subject>non-asthmatic eosinophilic bronchitis</subject><subject>Pneumonia - metabolism</subject><subject>Respiratory Function Tests</subject><issn>1323-7799</issn><issn>1440-1843</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEFPwyAYhonROJ3-BcPJWysFWuBiYpY5TYwum8YjwUIds2tnYbP791K76FUuvIT3e77kAQAmKE7CuVrGCaUoSjglMUaIxyjBjMTtATj5_TgMmWASMSbEAJw6t0QIkRSlx2CQcCIET9kJmI3bhSqNhpX1jc1h3VptYGm2pnTQVnCtvDWVd_DL-gVUvl6HUl5v3sOj0vu0VY1VlYfK-cVKnYGjQpXOnO_vIXi5HT-P7qKHp8n96OYhylOckYgibRTlmS5QnheMKlxQVmD-hjDDmVZakAynjNGCaJJpjjRTgmOhqGFUFIgMwWXPXTf158Y4L1fW5aYsVWXqjZMMBbqgSSjyvpg3tXONKeS6sSvV7GSCZOdTLmWnTXbaZOdT_viUbRi92O_YvK2M_hvcCwyF677wZUuz-zdYzsbzaRcDIOoB1nnT_gJU8yEzRlgqXx8nUsxHk9l8SiQl316yk04</recordid><startdate>200805</startdate><enddate>200805</enddate><creator>FUJIMURA, Masaki</creator><creator>OHKURA, Noriyuki</creator><creator>ABO, Miki</creator><creator>FURUSHO, Shiho</creator><creator>WASEDA, Yuko</creator><creator>ICHIKAWA, Yukari</creator><creator>HARA, Johsuke</creator><general>Blackwell Publishing Asia</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200805</creationdate><title>Exhaled nitric oxide levels in patients with atopic cough and cough variant asthma</title><author>FUJIMURA, Masaki ; OHKURA, Noriyuki ; ABO, Miki ; FURUSHO, Shiho ; WASEDA, Yuko ; ICHIKAWA, Yukari ; HARA, Johsuke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5263-40dea486df0ccf74a2f47f28b02726dad93625774f3d36d80d7a9829a4e749f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Asthma - diagnosis</topic><topic>Asthma - drug therapy</topic><topic>Asthma - metabolism</topic><topic>atopic cough</topic><topic>Biomarkers - metabolism</topic><topic>Breath Tests</topic><topic>bronchial asthma</topic><topic>Bronchial Provocation Tests</topic><topic>Bronchodilator Agents - therapeutic use</topic><topic>Case-Control Studies</topic><topic>Cough - diagnosis</topic><topic>Cough - drug therapy</topic><topic>Cough - metabolism</topic><topic>cough variant asthma</topic><topic>Cross-Sectional Studies</topic><topic>Diagnosis, Differential</topic><topic>exhaled nitric oxide</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nitric Oxide - metabolism</topic><topic>non-asthmatic eosinophilic bronchitis</topic><topic>Pneumonia - metabolism</topic><topic>Respiratory Function Tests</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FUJIMURA, Masaki</creatorcontrib><creatorcontrib>OHKURA, Noriyuki</creatorcontrib><creatorcontrib>ABO, Miki</creatorcontrib><creatorcontrib>FURUSHO, Shiho</creatorcontrib><creatorcontrib>WASEDA, Yuko</creatorcontrib><creatorcontrib>ICHIKAWA, Yukari</creatorcontrib><creatorcontrib>HARA, Johsuke</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Respirology (Carlton, Vic.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FUJIMURA, Masaki</au><au>OHKURA, Noriyuki</au><au>ABO, Miki</au><au>FURUSHO, Shiho</au><au>WASEDA, Yuko</au><au>ICHIKAWA, Yukari</au><au>HARA, Johsuke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exhaled nitric oxide levels in patients with atopic cough and cough variant asthma</atitle><jtitle>Respirology (Carlton, Vic.)</jtitle><addtitle>Respirology</addtitle><date>2008-05</date><risdate>2008</risdate><volume>13</volume><issue>3</issue><spage>359</spage><epage>364</epage><pages>359-364</pages><issn>1323-7799</issn><eissn>1440-1843</eissn><abstract>Background and objective:  Atopic cough (AC) is an established clinical entity in Japan, in which patients present with a chronic persistent non‐productive cough. Exhaled nitric oxide (NO) is a biomarker of eosinophilic airway inflammation. The present study examined whether exhaled NO levels were increased in AC in comparison with cough variant asthma (CVA) and bronchial asthma (BA). Methods:  Consecutive patients presenting with an isolated cough lasting at least 8 weeks were enrolled in the study. The aetiology of the chronic cough was determined according to the Japanese Respiratory Society guidelines for management of cough. Exhaled NO, capsaicin cough sensitivity (capsaicin concentration eliciting five or more coughs (C5)) and bronchial reversibility were measured at the patients’ first visit. Bronchial responsiveness (PC20 to methacholine) was measured at their second visit following a 6‐day course of bronchodilator therapy. Results:  There were 58 patients recruited and fully investigated; of these 9 and 11 patients were diagnosed with AC and CVA, respectively, as single causes of chronic cough. Ten patients with BA who had not received corticosteroid therapy in the previous 4 weeks and who attended the same clinic in the same time period acted as controls. Exhaled NO levels in patients with AC were significantly lower than those in patients with CVA and BA. There was no significant difference in the exhaled NO levels between patients with CVA and BA. Conclusions:  Exhaled NO may reflect eosinophilic inflammation of peripheral airways and its measurement may be useful in differentiating CVA from AC and other causes of chronic non‐productive cough.</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Publishing Asia</pub><pmid>18399857</pmid><doi>10.1111/j.1440-1843.2008.01273.x</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1323-7799
ispartof Respirology (Carlton, Vic.), 2008-05, Vol.13 (3), p.359-364
issn 1323-7799
1440-1843
language eng
recordid cdi_proquest_miscellaneous_70486941
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adult
Asthma - diagnosis
Asthma - drug therapy
Asthma - metabolism
atopic cough
Biomarkers - metabolism
Breath Tests
bronchial asthma
Bronchial Provocation Tests
Bronchodilator Agents - therapeutic use
Case-Control Studies
Cough - diagnosis
Cough - drug therapy
Cough - metabolism
cough variant asthma
Cross-Sectional Studies
Diagnosis, Differential
exhaled nitric oxide
Female
Humans
Male
Middle Aged
Nitric Oxide - metabolism
non-asthmatic eosinophilic bronchitis
Pneumonia - metabolism
Respiratory Function Tests
title Exhaled nitric oxide levels in patients with atopic cough and cough variant asthma
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T19%3A27%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Exhaled%20nitric%20oxide%20levels%20in%20patients%20with%20atopic%20cough%20and%20cough%20variant%20asthma&rft.jtitle=Respirology%20(Carlton,%20Vic.)&rft.au=FUJIMURA,%20Masaki&rft.date=2008-05&rft.volume=13&rft.issue=3&rft.spage=359&rft.epage=364&rft.pages=359-364&rft.issn=1323-7799&rft.eissn=1440-1843&rft_id=info:doi/10.1111/j.1440-1843.2008.01273.x&rft_dat=%3Cproquest_cross%3E70486941%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=70486941&rft_id=info:pmid/18399857&rfr_iscdi=true