Marieann Högman, Christer Janson, Andreas Palm, Björn Ställberg, Kristina Bröms, Karin Lisspers, Maria Hårdstedt, Amir Farkhooy, Andrei Malinovschi
{"title":"两年内呼出一氧化氮稳定性与COPD结果的关系。","authors":"Marieann Högman, Christer Janson, Andreas Palm, Björn Ställberg, Kristina Bröms, Karin Lisspers, Maria Hårdstedt, Amir Farkhooy, Andrei Malinovschi","doi":"10.1088/1752-7163/adfd04","DOIUrl":null,"url":null,"abstract":"<p><p>The non-invasive biological marker exhaled nitric oxide (FE<sub>NO</sub>) is increasingly used in asthma, but its clinical role in COPD is less established. FE<sub>NO</sub>has been reported to be both high and low outside the COPD exacerbation period. The study aimed to follow FE<sub>NO</sub>values over two years during stable conditions in a cohort of COPD subjects participating in the TIE-study (Tools Identifying Exacerbation). The follow-up study included 353 subjects who attended three visits one year apart. The subjects that were ex-smokers (<i>n</i>= 265) had higher FE<sub>NO,50</sub>values (median and IQR) compared with current smokers (<i>n</i>= 88), at inclusion 15 (10, 24) versus 9 (7, 15) ppb, after one year 15 (10, 24) versus 10 (7, 18) ppb, and after two years 14 (9, 22) versus 10 (7, 17) ppb, all<i>p</i>< 0.001. All subjects were further divided into two FE<sub>NO</sub>groups: <20 ppb (72%) and ⩾20 ppb (28%). After one year, 81% of the participants remained in the low group and 65% in the high FE<sub>NO</sub>group. After two years, 71% remained in the low group and 52% in the high FE<sub>NO</sub>group. The persistent low FE<sub>NO</sub>group had statistically significantly lower FEV<sub>1</sub>%pred and FVC%pred compared to the high FE<sub>NO</sub>group for all three visits. Among the ex-smokers, the proportion of subjects reporting dyspnoea (mMRC ⩾ 2) was higher in the persistent low FE<sub>NO</sub>group than in the persistent high FE<sub>NO</sub>group at all three visits. In conclusion, good consistency in FE<sub>NO</sub>over two years is promising for monitoring FE<sub>NO</sub>during stable disease. COPD subjects with persistent low FE<sub>NO</sub>had poorer lung function and reported more dyspnoea than subjects with persistent high FE<sub>NO</sub>.</p>","PeriodicalId":15306,"journal":{"name":"Journal of breath research","volume":" ","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Exhaled nitric oxide stability over two years in relation to COPD outcomes.\",\"authors\":\"Marieann Högman, Christer Janson, Andreas Palm, Björn Ställberg, Kristina Bröms, Karin Lisspers, Maria Hårdstedt, Amir Farkhooy, Andrei Malinovschi\",\"doi\":\"10.1088/1752-7163/adfd04\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The non-invasive biological marker exhaled nitric oxide (FE<sub>NO</sub>) is increasingly used in asthma, but its clinical role in COPD is less established. FE<sub>NO</sub>has been reported to be both high and low outside the COPD exacerbation period. The study aimed to follow FE<sub>NO</sub>values over two years during stable conditions in a cohort of COPD subjects participating in the TIE-study (Tools Identifying Exacerbation). The follow-up study included 353 subjects who attended three visits one year apart. The subjects that were ex-smokers (<i>n</i>= 265) had higher FE<sub>NO,50</sub>values (median and IQR) compared with current smokers (<i>n</i>= 88), at inclusion 15 (10, 24) versus 9 (7, 15) ppb, after one year 15 (10, 24) versus 10 (7, 18) ppb, and after two years 14 (9, 22) versus 10 (7, 17) ppb, all<i>p</i>< 0.001. All subjects were further divided into two FE<sub>NO</sub>groups: <20 ppb (72%) and ⩾20 ppb (28%). After one year, 81% of the participants remained in the low group and 65% in the high FE<sub>NO</sub>group. After two years, 71% remained in the low group and 52% in the high FE<sub>NO</sub>group. The persistent low FE<sub>NO</sub>group had statistically significantly lower FEV<sub>1</sub>%pred and FVC%pred compared to the high FE<sub>NO</sub>group for all three visits. Among the ex-smokers, the proportion of subjects reporting dyspnoea (mMRC ⩾ 2) was higher in the persistent low FE<sub>NO</sub>group than in the persistent high FE<sub>NO</sub>group at all three visits. In conclusion, good consistency in FE<sub>NO</sub>over two years is promising for monitoring FE<sub>NO</sub>during stable disease. COPD subjects with persistent low FE<sub>NO</sub>had poorer lung function and reported more dyspnoea than subjects with persistent high FE<sub>NO</sub>.</p>\",\"PeriodicalId\":15306,\"journal\":{\"name\":\"Journal of breath research\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-08-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of breath research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1088/1752-7163/adfd04\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of breath research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1088/1752-7163/adfd04","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
Exhaled nitric oxide stability over two years in relation to COPD outcomes.
The non-invasive biological marker exhaled nitric oxide (FENO) is increasingly used in asthma, but its clinical role in COPD is less established. FENOhas been reported to be both high and low outside the COPD exacerbation period. The study aimed to follow FENOvalues over two years during stable conditions in a cohort of COPD subjects participating in the TIE-study (Tools Identifying Exacerbation). The follow-up study included 353 subjects who attended three visits one year apart. The subjects that were ex-smokers (n= 265) had higher FENO,50values (median and IQR) compared with current smokers (n= 88), at inclusion 15 (10, 24) versus 9 (7, 15) ppb, after one year 15 (10, 24) versus 10 (7, 18) ppb, and after two years 14 (9, 22) versus 10 (7, 17) ppb, allp< 0.001. All subjects were further divided into two FENOgroups: <20 ppb (72%) and ⩾20 ppb (28%). After one year, 81% of the participants remained in the low group and 65% in the high FENOgroup. After two years, 71% remained in the low group and 52% in the high FENOgroup. The persistent low FENOgroup had statistically significantly lower FEV1%pred and FVC%pred compared to the high FENOgroup for all three visits. Among the ex-smokers, the proportion of subjects reporting dyspnoea (mMRC ⩾ 2) was higher in the persistent low FENOgroup than in the persistent high FENOgroup at all three visits. In conclusion, good consistency in FENOover two years is promising for monitoring FENOduring stable disease. COPD subjects with persistent low FENOhad poorer lung function and reported more dyspnoea than subjects with persistent high FENO.
期刊介绍:
Journal of Breath Research is dedicated to all aspects of scientific breath research. The traditional focus is on analysis of volatile compounds and aerosols in exhaled breath for the investigation of exogenous exposures, metabolism, toxicology, health status and the diagnosis of disease and breath odours. The journal also welcomes other breath-related topics.
Typical areas of interest include:
Big laboratory instrumentation: describing new state-of-the-art analytical instrumentation capable of performing high-resolution discovery and targeted breath research; exploiting complex technologies drawn from other areas of biochemistry and genetics for breath research.
Engineering solutions: developing new breath sampling technologies for condensate and aerosols, for chemical and optical sensors, for extraction and sample preparation methods, for automation and standardization, and for multiplex analyses to preserve the breath matrix and facilitating analytical throughput. Measure exhaled constituents (e.g. CO2, acetone, isoprene) as markers of human presence or mitigate such contaminants in enclosed environments.
Human and animal in vivo studies: decoding the ''breath exposome'', implementing exposure and intervention studies, performing cross-sectional and case-control research, assaying immune and inflammatory response, and testing mammalian host response to infections and exogenous exposures to develop information directly applicable to systems biology. Studying inhalation toxicology; inhaled breath as a source of internal dose; resultant blood, breath and urinary biomarkers linked to inhalation pathway.
Cellular and molecular level in vitro studies.
Clinical, pharmacological and forensic applications.
Mathematical, statistical and graphical data interpretation.