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      Plasma YKL-40 and NGAL are useful in distinguishing ACO from asthma and COPD

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          Abstract

          Background

          Asthma-chronic obstructive pulmonary disorder (COPD) overlap (ACO) is characterized by the coexistence of features of both asthma and COPD and is associated with rapid progress and a poor prognosis. Thus, the early recognition of ACO is crucial.

          Objectives

          We sought to explore the plasma levels of biomarkers associated with asthma (periostin, TSLP and YKL-40), COPD (NGAL) and their possible correlation with lung function, the bronchodilator response and radiographic imaging in patients with asthma, COPD and with features of ACO.

          Methods

          We enrolled 423 subjects from 6 clinical centers. All participants underwent blood collection, lung function measurements, bronchodilator response tests and high-resolution CT. Correlations of the plasma biomarkers with lung function, the bronchodilator response and percentemphysema were calculated by Spearman’s rank correlation and multivariate stepwise regressionanalysis.

          Results

          1) Patients with features of ACO had lower plasma YKL-40 than COPD patients and a moderate elevated plasma level of NGAL compared with asthma patients. 2) Patients with features of ACO had an intermediate degree of airflow obstruction, the bronchodilator response and emphysema between patients with COPD and asthma. 3) Plasma YKL-40 was negatively correlated with lung function and with the bronchodilator response, and plasma NGAL was positively correlated with the extent of emphysema.

          Conclusions

          Plasma YKL-40 is a promising candidate for distinguishing between patients with features of ACO and COPD patients, while plasma NGAL may be a valuable biomarker for differentiating between patients with features of ACO and asthma patients.

          Clinical trial registration

          ChiCTR-OOC-16009221.

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          Most cited references29

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          The Asthma-COPD Overlap Syndrome.

          Although in textbooks asthma and chronic obstructive pulmonary disease (COPD) are viewed as distinct disorders, there is increasing awareness that many patients have features of both. This article reviews the asthma-COPD overlap syndrome.
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            Increased risk of exacerbation and hospitalization in subjects with an overlap phenotype: COPD-asthma.

            Several COPD phenotypes have been described; the COPD-asthma overlap is one of the most recognized. The aim of this study was to evaluate the prevalence of three subgroups (asthma, COPD, and COPD-asthma overlap) in the Latin American Project for the Investigation of Obstructive Lung Disease (PLATINO) study population, to describe their main characteristics, and to determine the association of the COPD-asthma overlap group with exacerbations, hospitalizations, limitations due to physical health, and perception of general health status (GHS). The PLATINO study is a multicenter population-based survey carried out in five Latin American cities. Outcomes were self-reported exacerbations (defined by deterioration of breathing symptoms that affected usual daily activities or caused missed work), hospitalizations due to exacerbations, physical health limitations, and patients' perception of their GHS obtained by questionnaire. Subjects were classified in three specific groups: COPD--a postbronchodilator (post-BD) FEV₁/FVC ratio of < 0.70; asthma--presence of wheezing in the last year and a minimum post-BD increase in FEV₁ or FVC of 12% and 200 mL; and overlap COPD-asthma--the combination of the two. Out of 5,044 subjects, 767 were classified as having COPD (12%), asthma (1.7%), and COPD-asthma overlap (1.8%). Subjects with COPD-asthma overlap had more respiratory symptoms, had worse lung function, used more respiratory medication, had more hospitalization and exacerbations, and had worse GHS. After adjusting for confounders, the COPD-asthma overlap was associated with higher risks for exacerbations (prevalence ratio [PR], 2.11; 95% CI, 1.08-4.12), hospitalizations (PR, 4.11; 95% CI, 1.45-11.67), and worse GHS (PR, 1.47; 95% CI, 1.18-1.85) compared with those with COPD. The coexisting COPD-asthma phenotype is possibly associated with increased disease severity.
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              Thymic stromal lymphopoietin: master switch for allergic inflammation

              Thymic stromal lymphopoietin (TSLP) is an interleukin (IL) 7–like cytokine that triggers dendritic cell–mediated T helper (Th)2 inflammatory responses. TSLP is highly expressed by keratinocytes in skin lesions of patients with atopic dermatitis and is associated with dendritic cell activation in situ, suggesting that TSLP might be a master switch for allergic inflammation at the epithelial cell–dendritic cell interface. New reports now establish a direct link between TSLP expression and the pathogenesis of atopic dermatitis and asthma in vivo, and begin to reveal the molecular mechanisms underlying TSLP-induced allergic inflammation.
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                Author and article information

                Contributors
                congrong2008@163.com
                1210707650@qq.com
                skyny4511@126.com
                1247646346@qq.com
                1339812570@qq.com
                441026985@qq.com
                190728092@qq.com
                zengzuo1992@sina.com
                233420684@qq.com
                2637056467@qq.com
                489630931@qq.com
                524697592@qq.com
                depengjiang@163.com
                Journal
                Respir Res
                Respir. Res
                Respiratory Research
                BioMed Central (London )
                1465-9921
                1465-993X
                27 March 2018
                27 March 2018
                2018
                : 19
                : 47
                Affiliations
                [1 ]ISNI 0000 0000 8653 0555, GRID grid.203458.8, Department of Respiratory Medicine, , the Second Clinical Hospital of Chongqing Medical University, ; Chongqing, 400010 China
                [2 ]ISNI 0000 0000 9588 0960, GRID grid.285847.4, Department of Respiratory Medicine, , the First Clinical Hospital of Kunming Medical University, ; Kunming, 650032 Yunnan Province China
                [3 ]ISNI 0000 0000 8653 0555, GRID grid.203458.8, Department of Laboratory Medicine, , the Second Clinical Hospital of Chongqing Medical University, ; Chongqing, 400010 China
                [4 ]GRID grid.440164.3, Department of Respiratory Medicine, , Chengdu Second People’s Hospital, ; Chengdu, 610011 Sichuan Province China
                [5 ]Department of Respiratory Medicine, People’s Hospital of Wuxi Country, Chongqing, 405800 China
                [6 ]Department of Respiratory Medicine, People’s Hospital of Shizhu Country, Chongqing, 409100 China
                [7 ]Department of Respiratory Medicine, People’s Hospital of Fengjie Country, Chongqing, 404600 China
                Article
                755
                10.1186/s12931-018-0755-6
                5870925
                29580282
                fa6eb544-34c5-4f77-a3be-cd29429a3c3f
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 26 January 2018
                : 21 March 2018
                Funding
                Funded by: the Health and Family Planning Commission of Chongqing City
                Award ID: 2016HBRC004
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Respiratory medicine
                asthma copd overlap (aco),chronic obstructive pulmonary disease,asthma,ykl-40,ngal

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