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      Anemia and Adverse Outcomes in a Chronic Obstructive Pulmonary Disease Population with a High Burden of Comorbidities. An Analysis from SPIROMICS

      1 , 1 , 1 , 1 , 2 , 1 , 1 , 3 , 4 , 5 , 6 , 4 , 4 , 1 , 7 , 1 , 5 , 8 , 1 , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,
      Annals of the American Thoracic Society
      American Thoracic Society

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          Abstract

          <p class="first" id="d841461e718"> <b>Rationale:</b> Chronic obstructive pulmonary disease (COPD) is a common cause of morbidity and associated with a significant burden of comorbidities. Although anemia is associated with adverse outcomes in COPD, its contribution to outcomes in individuals with other comorbid chronic diseases is not well understood. </p><p id="d841461e723"> <b>Objectives:</b> This study examines the association of anemia with outcomes in a large, well-characterized COPD cohort, and attempts to understand the contribution of anemia to outcomes and phenotypes in individuals with other comorbidities. </p><p id="d841461e728"> <b>Methods:</b> Participants with COPD from SPIROMICS (the Subpopulations and Intermediate Outcome Measures in COPD Study) were analyzed in adjusted models to determine the associations of normocytic anemia with clinical outcomes, computed tomographic measures, and biomarkers. Analysis was additionally performed to understand the independence and possible interactions related to cardiac and metabolic comorbidities. </p><p id="d841461e733"> <b>Results:</b> A total of 1,789 individuals with COPD from SPIROMICS had data on hemoglobin, and of these 7.5% ( <i>n</i> = 135) were found to have normocytic anemia. Anemic participants were older with worse airflow obstruction, a higher proportion of them were African Americans, and they had a higher burden of cardiac and metabolic comorbidities. Anemia was strongly associated with 6-minute walk distance (β, −61.43; 95% confidence interval [CI], −85.11 to −37.75), modified Medical Research Council dyspnea questionnaire (β, 0.27; 95% CI, 0.11–0.44), and St. George’s Respiratory Questionnaire (β, 3.90; 95% CI, 1.09–6.71), and these adjusted associations were stronger among those with two or more cardiac and metabolic comorbidities. Anemia was associated with higher levels of serum C-reactive protein, soluble receptor for advanced glycosylation end-products, and epithelial cadherin-1, findings that persisted when in those with a high burden of comorbidities. </p><p id="d841461e741"> <b>Conclusions:</b> Anemia is associated with worse exercise capacity, greater dyspnea, and greater disease severity among adults with COPD, particularly among those with comorbid chronic cardiac and metabolic diseases. The biomarkers found in anemic individuals suggest inflammation, lung tissue injury, and oxidative stress as possible pathways for the adverse correlations of anemia with outcomes in COPD; however, substantial further study is required to better understand these potential mechanisms. </p><p id="d841461e746">Clinical trial registered with <a data-untrusted="" href="http://www.clinicaltrials.gov" id="d841461e748" target="xrefwindow">www.clinicaltrials.gov</a> (NCT01969344). </p>

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          Most cited references22

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          Design of the Subpopulations and Intermediate Outcomes in COPD Study (SPIROMICS).

          Subpopulations and Intermediate Outcomes in COPD Study (SPIROMICS) is a multicentre observational study of chronic obstructive pulmonary disease (COPD) designed to guide future development of therapies for COPD by providing robust criteria for subclassifying COPD participants into groups most likely to benefit from a given therapy during a clinical trial, and identifying biomarkers/phenotypes that can be used as intermediate outcomes to reliably predict clinical benefit during therapeutic trials. The goal is to enrol 3200 participants in four strata. Participants undergo a baseline visit and three annual follow-up examinations, with quarterly telephone calls. Adjudication of exacerbations and mortality will be undertaken.
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            Identification and prospective validation of clinically relevant chronic obstructive pulmonary disease (COPD) subtypes.

            Chronic obstructive pulmonary disease (COPD) is increasingly considered a heterogeneous condition. It was hypothesised that COPD, as currently defined, includes different clinically relevant subtypes. To identify and validate COPD subtypes, 342 subjects hospitalised for the first time because of a COPD exacerbation were recruited. Three months after discharge, when clinically stable, symptoms and quality of life, lung function, exercise capacity, nutritional status, biomarkers of systemic and bronchial inflammation, sputum microbiology, CT of the thorax and echocardiography were assessed. COPD groups were identified by partitioning cluster analysis and validated prospectively against cause-specific hospitalisations and all-cause mortality during a 4 year follow-up. Three COPD groups were identified: group 1 (n=126, 67 years) was characterised by severe airflow limitation (postbronchodilator forced expiratory volume in 1 s (FEV(1)) 38% predicted) and worse performance in most of the respiratory domains of the disease; group 2 (n=125, 69 years) showed milder airflow limitation (FEV(1) 63% predicted); and group 3 (n=91, 67 years) combined a similarly milder airflow limitation (FEV(1) 58% predicted) with a high proportion of obesity, cardiovascular disorders, diabetes and systemic inflammation. During follow-up, group 1 had more frequent hospitalisations due to COPD (HR 3.28, p<0.001) and higher all-cause mortality (HR 2.36, p=0.018) than the other two groups, whereas group 3 had more admissions due to cardiovascular disease (HR 2.87, p=0.014). In patients with COPD recruited at their first hospitalisation, three different COPD subtypes were identified and prospectively validated: 'severe respiratory COPD', 'moderate respiratory COPD', and 'systemic COPD'.
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              SPIROMICS Protocol for Multicenter Quantitative Computed Tomography to Phenotype the Lungs.

              Multidetector row computed tomography (MDCT) is increasingly taking a central role in identifying subphenotypes within chronic obstructive pulmonary disease (COPD), asthma, and other lung-related disease populations, allowing for the quantification of the amount and distribution of altered parenchyma along with the characterization of airway and vascular anatomy. The embedding of quantitative CT (QCT) into a multicenter trial with a variety of scanner makes and models along with the variety of pressures within a clinical radiology setting has proven challenging, especially in the context of a longitudinal study. SPIROMICS (Subpopulations and Intermediate Outcome Measures in COPD Study), sponsored by the National Institutes of Health, has established a QCT lung assessment system (QCT-LAS), which includes scanner-specific imaging protocols for lung assessment at total lung capacity and residual volume. Also included are monthly scanning of a standardized test object and web-based tools for subject registration, protocol assignment, and data transmission coupled with automated image interrogation to assure protocol adherence. The SPIROMICS QCT-LAS has been adopted and contributed to by a growing number of other multicenter studies in which imaging is embedded. The key components of the SPIROMICS QCT-LAS along with evidence of implementation success are described herein. While imaging technologies continue to evolve, the required components of a QCT-LAS provide the framework for future studies, and the QCT results emanating from SPIROMICS and the growing number of other studies using the SPIROMICS QCT-LAS will provide a shared resource of image-derived pulmonary metrics.
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                Author and article information

                Journal
                Annals of the American Thoracic Society
                Annals ATS
                American Thoracic Society
                2329-6933
                2325-6621
                June 2018
                June 2018
                : 15
                : 6
                : 710-717
                Affiliations
                [1 ]Division of Pulmonary and Critical Care Medicine, Department of Medicine and
                [2 ]Division of General Pediatrics and Adolescent Medicine, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland
                [3 ]University of Alabama at Birmingham, Birmingham, Alabama
                [4 ]University of Michigan Medical School, Ann Arbor, Michigan
                [5 ]Marsico Lung Institute, University of North Carolina School of Medicine, Chapel Hill, North Carolina
                [6 ]University of Utah School of Medicine, Salt Lake City, Utah
                [7 ]Cornell University School of Medicine, New York, New York; and
                [8 ]Columbia University Medical Center, New York, New York
                Article
                10.1513/AnnalsATS.201708-687OC
                6207135
                30726108
                c89375ef-3179-4443-b33e-52996500007a
                © 2018
                History

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