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      Practical surrogate marker of pulmonary dysanapsis by simple spirometry: an observational case–control study in primary care

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          Abstract

          Background

          We see patients who present with spirometry airflow limitation despite their forced expiratory volume in one second (FEV 1) as well as forced vital capacity (FVC) to be supernormal (FEV 1/FVC < 70%, both the %FEV 1 and the %FVC ≧100%) in asymptomatic healthy non-smokers. Based on previous studies, we hypothesized these spirometry conditions (results measured with spirometry) could be suitably used as a practical surrogate marker of pulmonary dysanapsis: the condition of disproportionate but physiologically normal growth between airways and lung parenchyma.

          Methods

          We compared the conventional surrogate marker of dysanapsis, maximum mid-expiratory flow to FVC (MMF/FVC), in SUBJECTS (FEV 1/FVC < 70%, both the %FEV 1 and the %FVC ≧100% in healthy non-smokers) (n = 25), in EMPHYSEMA (CT confirmed pulmonary emphysema, same spirometry results with SUBJECTS) (n = 55), and in CONTROLS (age- and height- matched, normal spirometry results) (n = 25). Next we added imaging analysis to evaluate the relationship between the cross sectional airway luminal area (X-Ai) and the lung volume results among the three groups.

          Results

          The MMF/FVC was significantly lower in SUBJECTS and in EMPHYSEMA compared to CONTROLS. However, percent predicted peak expiratory flow (%PEFR) was significantly lower only in SUBJECTS and not in EMPHYSEMA compared to CONTROLS. The ratio of the X-Ai of the trachea and right apical bronchus to lung volume was significantly lower in SUBJECTS compared to CONTROLS.

          Conclusion

          The simple spirometry conditions in SUBJECTS are highly suggestive of practical surrogate marker of pulmonary dysanapsis. Awareness of this concept would help to attenuate the risk of overdiagnosis of obstructive pulmonary disease.

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          Most cited references32

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          Site and nature of airway obstruction in chronic obstructive lung disease.

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            Computed tomography in pulmonary emphysema.

            Fifty-three patients with chronic obstructive airways disease and 19 age-matched controls were studied using computed tomography (CT). The study shows that CT can detect the presence and distribution of pulmonary emphysema. Pulmonary vascular changes detectable on chest radiography correlate well with lung density as measured by CT. Patients with marked CT changes of emphysema had significantly greater impairment of diffusion capacity and FEV1.0/VC than the patients with less severe changes.
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              Population impact of different definitions of airway obstruction.

              There is currently no consensus on the criteria for diagnosing chronic obstructive pulmonary disease. This study evaluated the impact of different definitions of airway obstruction on the estimated prevalence of obstruction in a population-based sample. Using the Third National Health and Nutrition Examination Survey, obstructive airway disease was defined using the following criteria: 1) self-reported diagnosis of chronic bronchitis or emphysema; 2) forced expiratory volume in one second (FEV1)/forced vital capacity (FVC) 50 yrs, the fixed ratio criteria produced the highest rate estimates. For all subgroups tested, the GOLD Stage II criteria produced lower estimates than other spirometry-based definitions. Different definitions of obstruction may produce prevalence estimates that vary by >200%. International opinion leaders should agree upon a clear definition of chronic obstructive pulmonary disease that can serve as a population-based measurement criterion as well as a guide to clinicians.
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                Author and article information

                Contributors
                sshiota@jutendo.ac.jp
                koara@juntendo.ac.jp
                ka-suzz@juntendo.ac.jp
                yfukuchi@tea.ocn.ne.jp
                kztakaha@juntendo.ac.jp
                Journal
                BMC Fam Pract
                BMC Fam Pract
                BMC Family Practice
                BioMed Central (London )
                1471-2296
                26 March 2015
                26 March 2015
                2015
                : 16
                : 41
                Affiliations
                [ ]Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, 113-8421 Bunkyo-ku, Tokyo Japan
                [ ]Department of Radiology, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, 113-8421 Bunkyo-ku, Tokyo Japan
                Article
                255
                10.1186/s12875-015-0255-4
                4397705
                6e239329-5a65-4256-a916-c20cd56bd62b
                © Shiota et al.; licensee BioMed Central. 2015

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
                : 17 January 2015
                : 9 March 2015
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2015

                Medicine
                dysanapsis,airflow limitation,spirometry,surrogate marker
                Medicine
                dysanapsis, airflow limitation, spirometry, surrogate marker

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