Marieann Högman, Hà Pham-Ngoc, Bô Nguyen-Duy, Jens Ellingsen, Thông Hua-Huy, Dinh Van Nguyen, Anh Tuan Dinh-Xuan
{"title":"Measuring exhaled nitric oxide in COPD: from theoretical consideration to practical views.","authors":"Marieann Högman, Hà Pham-Ngoc, Bô Nguyen-Duy, Jens Ellingsen, Thông Hua-Huy, Dinh Van Nguyen, Anh Tuan Dinh-Xuan","doi":"10.1080/17476348.2024.2433537","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Chronic obstructive pulmonary disease (COPD) is traditionally perceived as Th1-inflammation, but some patients have Th2-inflammation. A high fraction of exhaled nitric oxide (FE<sub>NO</sub>) is seen in asthma with Th2-inflammation, justifying FE<sub>NO</sub> as a point-of-care biomarker. The use of FE<sub>NO</sub> in COPD is much less frequent. We aimed to review the evidence in favor of FE<sub>NO</sub> measurement in COPD and discuss its potential usefulness in clinical settings.</p><p><strong>Areas covered: </strong>This review covers nitric oxide production in the airways and FE<sub>NO</sub> measurements in COPD patients during stable conditions and acute exacerbation. It discusses why COPD patients may have both low and high FE<sub>NO</sub> levels and the potential clinical utility of FE<sub>NO</sub>.</p><p><strong>Expert opinion: </strong>There is good evidence that FE<sub>NO</sub> increases with an exacerbation irrespective of the initial low or high baseline value. However, there is insufficient evidence to establish a fixed cutoff value for elevated FE<sub>NO</sub> in COPD today. Instead, a personal baseline FE<sub>NO</sub> level should be established when the patient is in a stable phase of the disease, which will subsequently set high and low FE<sub>NO</sub> levels in a personalized manner. In the future, home monitoring of FE<sub>NO</sub> could help identify exacerbations early, allowing proper action to be taken.</p>","PeriodicalId":94007,"journal":{"name":"Expert review of respiratory medicine","volume":" ","pages":"1-12"},"PeriodicalIF":0.0000,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Expert review of respiratory medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/17476348.2024.2433537","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Chronic obstructive pulmonary disease (COPD) is traditionally perceived as Th1-inflammation, but some patients have Th2-inflammation. A high fraction of exhaled nitric oxide (FENO) is seen in asthma with Th2-inflammation, justifying FENO as a point-of-care biomarker. The use of FENO in COPD is much less frequent. We aimed to review the evidence in favor of FENO measurement in COPD and discuss its potential usefulness in clinical settings.
Areas covered: This review covers nitric oxide production in the airways and FENO measurements in COPD patients during stable conditions and acute exacerbation. It discusses why COPD patients may have both low and high FENO levels and the potential clinical utility of FENO.
Expert opinion: There is good evidence that FENO increases with an exacerbation irrespective of the initial low or high baseline value. However, there is insufficient evidence to establish a fixed cutoff value for elevated FENO in COPD today. Instead, a personal baseline FENO level should be established when the patient is in a stable phase of the disease, which will subsequently set high and low FENO levels in a personalized manner. In the future, home monitoring of FENO could help identify exacerbations early, allowing proper action to be taken.