Predictive value of fractional nitric oxide in asthma diagnosis-subgroup analyses

•Children with atopy and allergic rhinitis have high levels of FeNO.•Age of children, allergy profile, lung function do not affected the FeNO level.•Negative predictive value of FeNO for asthma diagnosis in children is very high.•The optimal cut-off point of FeNO for asthma diagnosis in children is...

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Veröffentlicht in:Nitric oxide 2014-08, Vol.40, p.87-91
Hauptverfasser: Jerzyńska, Joanna, Majak, Paweł, Janas, Anna, Stelmach, Rafał, Stelmach, Włodzimierz, Smejda, Katarzyna, Stelmach, Iwona
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container_end_page 91
container_issue
container_start_page 87
container_title Nitric oxide
container_volume 40
creator Jerzyńska, Joanna
Majak, Paweł
Janas, Anna
Stelmach, Rafał
Stelmach, Włodzimierz
Smejda, Katarzyna
Stelmach, Iwona
description •Children with atopy and allergic rhinitis have high levels of FeNO.•Age of children, allergy profile, lung function do not affected the FeNO level.•Negative predictive value of FeNO for asthma diagnosis in children is very high.•The optimal cut-off point of FeNO for asthma diagnosis in children is 23ppb.•We showed the utility of FeNO measurements to exclude asthma in children. There are no studies investigating the benefit of using FeNO measurements in correlation with sensitization to perennial and seasonal allergens in children with asthma. To define the group of children with respiratory symptoms in whose FeNO measurement has predictive value for asthma. We assessed the effect of age, allergy profile, atopy, lung function and the presence of allergic rhinitis on interpretation of FeNO levels for clinical applications. It was a retrospective, cross-sectional study. We evaluated data from medical documentation of 1767 children with symptoms of allergic diseases such as asthma and/or allergic rhinitis. We included in the analyses subjects who had the following tests done during diagnostic procedures (single measurement): FeNO, spirometry, specific IgE results. All subjects had undergone a minimum 3-years prospective clinical observation after the first FeNO measurement until the later assignment (or not) of an asthma/allergic rhinitis diagnosis. We included 1767 children into the analysis; asthma diagnosis was confirm in 1054 (59.6%) children. We showed that only atopy (OR: 1.9; 95%CI: 1.5–2.4) and presence of allergic rhinitis (OR: 1.6; 95%CI: 1.4–1.9) were independently associated with increased FeNO level. Only among patients with atopy and allergic rhinitis FeNO level (above 23ppb) was associated with asthma diagnosis. Sensitivity, specificity, positive predictive value and negative predictive value of FeNO >23ppb for asthma diagnosis were as follows: 0.9(95%CI: 0.68–0.98), 0.52(95%CI: 0.42–0.61), 0.25(95%CI: 0.16–0.37), 0.97(95%CI: 0.88–0.99). We showed that in children with atopy and with allergic rhinitis a negative predictive value for asthma diagnosis was very high with the optimal cut-off point of FeNO 23ppb. Therefore we showed the utility of FeNO measurements to exclude asthma in the subgroup of patients with atopy and allergic rhinitis.
doi_str_mv 10.1016/j.niox.2014.06.001
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There are no studies investigating the benefit of using FeNO measurements in correlation with sensitization to perennial and seasonal allergens in children with asthma. To define the group of children with respiratory symptoms in whose FeNO measurement has predictive value for asthma. We assessed the effect of age, allergy profile, atopy, lung function and the presence of allergic rhinitis on interpretation of FeNO levels for clinical applications. It was a retrospective, cross-sectional study. We evaluated data from medical documentation of 1767 children with symptoms of allergic diseases such as asthma and/or allergic rhinitis. We included in the analyses subjects who had the following tests done during diagnostic procedures (single measurement): FeNO, spirometry, specific IgE results. All subjects had undergone a minimum 3-years prospective clinical observation after the first FeNO measurement until the later assignment (or not) of an asthma/allergic rhinitis diagnosis. We included 1767 children into the analysis; asthma diagnosis was confirm in 1054 (59.6%) children. We showed that only atopy (OR: 1.9; 95%CI: 1.5–2.4) and presence of allergic rhinitis (OR: 1.6; 95%CI: 1.4–1.9) were independently associated with increased FeNO level. Only among patients with atopy and allergic rhinitis FeNO level (above 23ppb) was associated with asthma diagnosis. Sensitivity, specificity, positive predictive value and negative predictive value of FeNO &gt;23ppb for asthma diagnosis were as follows: 0.9(95%CI: 0.68–0.98), 0.52(95%CI: 0.42–0.61), 0.25(95%CI: 0.16–0.37), 0.97(95%CI: 0.88–0.99). We showed that in children with atopy and with allergic rhinitis a negative predictive value for asthma diagnosis was very high with the optimal cut-off point of FeNO 23ppb. 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There are no studies investigating the benefit of using FeNO measurements in correlation with sensitization to perennial and seasonal allergens in children with asthma. To define the group of children with respiratory symptoms in whose FeNO measurement has predictive value for asthma. We assessed the effect of age, allergy profile, atopy, lung function and the presence of allergic rhinitis on interpretation of FeNO levels for clinical applications. It was a retrospective, cross-sectional study. We evaluated data from medical documentation of 1767 children with symptoms of allergic diseases such as asthma and/or allergic rhinitis. We included in the analyses subjects who had the following tests done during diagnostic procedures (single measurement): FeNO, spirometry, specific IgE results. All subjects had undergone a minimum 3-years prospective clinical observation after the first FeNO measurement until the later assignment (or not) of an asthma/allergic rhinitis diagnosis. We included 1767 children into the analysis; asthma diagnosis was confirm in 1054 (59.6%) children. We showed that only atopy (OR: 1.9; 95%CI: 1.5–2.4) and presence of allergic rhinitis (OR: 1.6; 95%CI: 1.4–1.9) were independently associated with increased FeNO level. Only among patients with atopy and allergic rhinitis FeNO level (above 23ppb) was associated with asthma diagnosis. Sensitivity, specificity, positive predictive value and negative predictive value of FeNO &gt;23ppb for asthma diagnosis were as follows: 0.9(95%CI: 0.68–0.98), 0.52(95%CI: 0.42–0.61), 0.25(95%CI: 0.16–0.37), 0.97(95%CI: 0.88–0.99). We showed that in children with atopy and with allergic rhinitis a negative predictive value for asthma diagnosis was very high with the optimal cut-off point of FeNO 23ppb. Therefore we showed the utility of FeNO measurements to exclude asthma in the subgroup of patients with atopy and allergic rhinitis.</description><subject>Adolescent</subject><subject>Asthma</subject><subject>Asthma - diagnosis</subject><subject>Asthma - metabolism</subject><subject>Child</subject><subject>Cross-Sectional Studies</subject><subject>Female</subject><subject>FeNO</subject><subject>Humans</subject><subject>Male</subject><subject>Nitric Oxide - analysis</subject><subject>Nitric Oxide - metabolism</subject><subject>Predictive Value of Tests</subject><subject>Prospective Studies</subject><subject>Respiratory Function Tests</subject><subject>Schoolchildren</subject><issn>1089-8603</issn><issn>1089-8611</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF1LwzAUhoMobk7_gBeSS29aT5I2bcEbGX7BQAW9DmmSzoyumUk7tn9vxuYuvTqHw_O-cB6ErgmkBAi_W6SddZuUAslS4CkAOUFjAmWVlJyQ0-MObIQuQlgAQMZKfo5GNKtomXMYo493b7RVvV0bvJbtYLBrcONlvLhOtrizvbcKu43VBtsOy9B_LyXWVs47F2xIwlDPvRtWWEZ8G0y4RGeNbIO5OswJ-np6_Jy-JLO359fpwyxRLOd9oqQs6wqAFqwminJe8lo1lJpCq0oXwHjFK11DkdG6KiWVmueEgGSy0QUtGjZBt_velXc_gwm9WNqgTNvKzrghCJLnjEAOhEWU7lHlXQjeNGLl7VL6rSAgdirFQuxUip1KAVxElTF0c-gf6qXRx8ifuwjc7wETv1xb40VQ1nQq-vRG9UI7-1__LxTUhdQ</recordid><startdate>20140831</startdate><enddate>20140831</enddate><creator>Jerzyńska, Joanna</creator><creator>Majak, Paweł</creator><creator>Janas, Anna</creator><creator>Stelmach, Rafał</creator><creator>Stelmach, Włodzimierz</creator><creator>Smejda, Katarzyna</creator><creator>Stelmach, Iwona</creator><general>Elsevier Inc</general><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>20140831</creationdate><title>Predictive value of fractional nitric oxide in asthma diagnosis-subgroup analyses</title><author>Jerzyńska, Joanna ; Majak, Paweł ; Janas, Anna ; Stelmach, Rafał ; Stelmach, Włodzimierz ; Smejda, Katarzyna ; Stelmach, Iwona</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-caa8b900273b1c26686bcf22e7dc9d7036969db0742b98a2ad65110a3afd727f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adolescent</topic><topic>Asthma</topic><topic>Asthma - diagnosis</topic><topic>Asthma - metabolism</topic><topic>Child</topic><topic>Cross-Sectional Studies</topic><topic>Female</topic><topic>FeNO</topic><topic>Humans</topic><topic>Male</topic><topic>Nitric Oxide - analysis</topic><topic>Nitric Oxide - metabolism</topic><topic>Predictive Value of Tests</topic><topic>Prospective Studies</topic><topic>Respiratory Function Tests</topic><topic>Schoolchildren</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jerzyńska, Joanna</creatorcontrib><creatorcontrib>Majak, Paweł</creatorcontrib><creatorcontrib>Janas, Anna</creatorcontrib><creatorcontrib>Stelmach, Rafał</creatorcontrib><creatorcontrib>Stelmach, Włodzimierz</creatorcontrib><creatorcontrib>Smejda, Katarzyna</creatorcontrib><creatorcontrib>Stelmach, Iwona</creatorcontrib><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>Nitric oxide</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jerzyńska, Joanna</au><au>Majak, Paweł</au><au>Janas, Anna</au><au>Stelmach, Rafał</au><au>Stelmach, Włodzimierz</au><au>Smejda, Katarzyna</au><au>Stelmach, Iwona</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predictive value of fractional nitric oxide in asthma diagnosis-subgroup analyses</atitle><jtitle>Nitric oxide</jtitle><addtitle>Nitric Oxide</addtitle><date>2014-08-31</date><risdate>2014</risdate><volume>40</volume><spage>87</spage><epage>91</epage><pages>87-91</pages><issn>1089-8603</issn><eissn>1089-8611</eissn><abstract>•Children with atopy and allergic rhinitis have high levels of FeNO.•Age of children, allergy profile, lung function do not affected the FeNO level.•Negative predictive value of FeNO for asthma diagnosis in children is very high.•The optimal cut-off point of FeNO for asthma diagnosis in children is 23ppb.•We showed the utility of FeNO measurements to exclude asthma in children. There are no studies investigating the benefit of using FeNO measurements in correlation with sensitization to perennial and seasonal allergens in children with asthma. To define the group of children with respiratory symptoms in whose FeNO measurement has predictive value for asthma. We assessed the effect of age, allergy profile, atopy, lung function and the presence of allergic rhinitis on interpretation of FeNO levels for clinical applications. It was a retrospective, cross-sectional study. We evaluated data from medical documentation of 1767 children with symptoms of allergic diseases such as asthma and/or allergic rhinitis. We included in the analyses subjects who had the following tests done during diagnostic procedures (single measurement): FeNO, spirometry, specific IgE results. All subjects had undergone a minimum 3-years prospective clinical observation after the first FeNO measurement until the later assignment (or not) of an asthma/allergic rhinitis diagnosis. We included 1767 children into the analysis; asthma diagnosis was confirm in 1054 (59.6%) children. We showed that only atopy (OR: 1.9; 95%CI: 1.5–2.4) and presence of allergic rhinitis (OR: 1.6; 95%CI: 1.4–1.9) were independently associated with increased FeNO level. Only among patients with atopy and allergic rhinitis FeNO level (above 23ppb) was associated with asthma diagnosis. Sensitivity, specificity, positive predictive value and negative predictive value of FeNO &gt;23ppb for asthma diagnosis were as follows: 0.9(95%CI: 0.68–0.98), 0.52(95%CI: 0.42–0.61), 0.25(95%CI: 0.16–0.37), 0.97(95%CI: 0.88–0.99). We showed that in children with atopy and with allergic rhinitis a negative predictive value for asthma diagnosis was very high with the optimal cut-off point of FeNO 23ppb. Therefore we showed the utility of FeNO measurements to exclude asthma in the subgroup of patients with atopy and allergic rhinitis.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24928560</pmid><doi>10.1016/j.niox.2014.06.001</doi><tpages>5</tpages></addata></record>
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subjects Adolescent
Asthma
Asthma - diagnosis
Asthma - metabolism
Child
Cross-Sectional Studies
Female
FeNO
Humans
Male
Nitric Oxide - analysis
Nitric Oxide - metabolism
Predictive Value of Tests
Prospective Studies
Respiratory Function Tests
Schoolchildren
title Predictive value of fractional nitric oxide in asthma diagnosis-subgroup analyses
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