| Literature DB >> 26789845 |
Abstract
OBJECTIVES: To understand the key characteristics of Asthma and Chronic Obstructive Pulmonary Disease Overlap Syndrome (ACOS) and to identify evidence gaps relating to the identification, treatment and management of ACOS patients.Entities:
Keywords: ACOS; Asthma; Asthma and Chronic Obstructive Pulmonary Disease Overlap Syndrome; COPD; Chronic Obstructive Pulmonary Disease; burden; health-related quality of life
Mesh:
Year: 2016 PMID: 26789845 PMCID: PMC4819878 DOI: 10.1586/17476348.2016.1144476
Source DB: PubMed Journal: Expert Rev Respir Med ISSN: 1747-6348 Impact factor: 3.772
Figure 1. Structured literature review–attrition of identified publications.
Reported prevalence of ACOS within the published literature.
| Source | Study design | Definition of ACOS | ACOS prevalence |
|---|---|---|---|
| Andersen | Hospital discharge registry data in Finland, covering the whole Finnish population (5.35 million, 2009). Patients >34 years of age and treatment periods from 2000 to 2009, with a primary or secondary diagnosis of COPD or asthma were identified ( | ICD-10 COPD or asthma plus treatment for both within the study period. | 16.1% in patients with primary or secondary diagnoses of COPD or asthma in Finland. |
| Miravitlles | A total of 385 patients with COPD (FEV1/FVC < 0.7) identified in the cross-sectional EPI-SCAN study cohort ( | All participants with spirometric-defined COPD (defined by a post-bronchodilator FEV1/FVC ratio of <0.70) were classified as overlap COPD-asthma subjects if they confirmed that they had previously been diagnosed with asthma. | 17.4% in subjects diagnosed with COPD in Spain ( |
| De Marco | A screening questionnaire on respiratory symptoms, diagnoses, and risk factors was administered by mail to a random sample of the general Italian population. | Self-reported physician diagnosis of ACOS. | 1.6%, 2.1%, and 4.5% of a sample of the Italian general population, aged 20–44, 45–64, and 65–84, respectively. |
| Izquierdo-Alonso | An observational multicenter study enrolling 331 COPD patients aged 40 or older from pulmonary outpatient centers. | Diffusion test with transfer factor of the lung for carbon monoxide ( | 12.1% of COPD patients ( |
| Fu | A 4 year prospective cohort study in adults aged >55 years with obstructive airway diseases in Australia ( | Respiratory symptoms, increased airflow variability (asthma, i.e. airway hyperresponsiveness), and incompletely reversible airway obstruction (COPD, i.e. post-bronchodilator FEV1/FVC <70%). | 55.5% in patients >55 years of age with obstructive airway disease ( |
| Milanese | An observational multicenter survey enrolling patients >64 years old with a documented physician diagnosis of asthma between October 2012 and March 2013 in Italy ( | A diagnosis of asthma plus chronic bronchitis and/or impaired CO diffusion test. | 29% in asthma patients >64 years of age ( |
| Yon-Lee | Retrospective medical record review of the clinical characteristics of asthma in- and outpatients aged 41‒79 years between September 2007 and March 2012 in South Korea( | Overlap patients were defined as patients with physician-diagnosed asthma (a positive response to bronchodilator (>200 mL FEV1 and >12% baseline) and/or positive methacholine or mannitol provocation test) and incompletely reversible airflow obstruction (post-bronchodilator FEV1/FVC <70) at admission and for ≥3 months regardless of treatment. | 38% in asthma patients aged 41–79 years ( |
| Marsh | A randomized, population-based survey including questionnaires, pulmonary function tests, and chest CT scans. | Patients with COPD (post-bronchodilator FEV1/FVC <0.7) and asthma (post-bronchodilator increase in FEV1 ≥ 15% or peak flow variability ≥20% during 1 week of testing or physician-diagnosed asthma in conjunction with current symptoms). | 55.2% in COPD patients >50 years of age ( |
| Zeki | A small cohort from the academic general pulmonary/asthma referral clinic was compared to patients from the severe asthma clinic (UC Davis Asthma Network (UCAN) Clinics). | ACOS was defined as one of two clinical phenotypes:
Allergic disease consistent with asthma (variable airflow obstruction or AHR) that is incompletely reversible (with or without emphysema or reduced carbon monoxide diffusion capacity). COPD with emphysema accompanied by reversible or partially reversible airflow obstruction (with or without an allergic component or reduced carbon monoxide diffusion capacity). | Of the small cohort from the academic general pulmonary clinic/asthma referral clinic, 15.8% of patients were ACOS compared to 34.2% asthma and 43.4% COPD/emphysema. In the severe asthma clinic, 24.3% of patients were ACOS compared to 52.9% of asthma. |
ACOS = Asthma and COPD overlap syndrome; AHR = Airway hyper responsiveness; CO = Carbon monoxide; COPD = Chronic obstructive pulmonary disease; CT = computed tomography; FVC = forced vital capacity; FEV1 = forced expiratory volume in 1 second; ICD-10 = international classification of disease criteria.
Figure 2. Terminology reported within the published literature to describe the overlap phenotype (n = 43).
Clinical and physiological characteristics of asthma, ACOS,and COPD [1,2,4,13,24].
| Measure | Asthma | ACOS | COPD |
|---|---|---|---|
| Symptoms | Intermittent, worse at night or in the morning | Progressively worsen | Progressively worsen |
| FEV1/FVC | ≥70% | <70% | <70% |
| FEV1 %predicted* | >80% | <80% | <80% |
| AHR, PD15^ | <12 ml | <12 ml | >12 ml |
| PB increase in FEV1 | ≥12% and 400 ml (marked reversibility) | ≥12% and ≥200 ml (reversible) | ≥12% and ≥200 ml (reversible) |
| FeNO | >50 ppb | 25–50 ppb | <25 ppb |
| DLco | Normal, although smokers may present with a lower DLco | Normal–low | <80% predicted |
| Imaging | Usually normal | Bronchial wall thickening, emphysema, gas trapping on expiratory chest CT scans, greater segmental wall area on inspiratory CT scans, fibrosis, hyperinflation | Bronchial wall thickening, emphysema, fibrosis, hyperinflation |
| Inflammation | Eosinophils > neutrophils, mast cells, CD4+ T lymphocytes | Eosinophils and neutrophils, CD4+ and CD8+ T lymphocytes | Neutrophils > eosinophils, CD4+, CD8+ T lymphocytes |
| IgE, IL-4/-5/-13, eotaxin | IgE, IL-4/-5/-13/-1β/-8/-6, TNF-α, eotaxin, proteases | IL-1β/-8/-6, TNF-α, proteases | |
| Test for atopy, (MAST) | Commonly allergic to environmental allergens | Commonly allergic to environmental allergens | Do not rule out COPD, ACOS may be more likely |
| Exacerbations | >3/year, well controlled by treatment | More frequent than asthma and COPD alone | >2/year |
*postbronchodilator, ^provocation dose of hypertonic saline that induces a 15% fall in FEV1.
AHR = airway hyperresponsiveness; COPD = Chronic obstructive pulmonary disease; CT = computed tomography; DLco = carbon monoxide diffusing capacity; FeNO = fraction of exhaled nitric oxide; FEV1 = forced expiratory volume in 1s; FVC = Forced vital capacity; IgE = immunoglobulin E; MAST= multiple allergens simultaneous test; PD = provocation dose; PB = post bronchodilator; TNF = tumour necrosis factor.