<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Agusti A</submitter><funding>Medical Research Council</funding><pagination>e37483</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3356313</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(5)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Because chronic obstructive pulmonary disease (COPD) is a heterogeneous condition, the identification of specific clinical phenotypes is key to developing more effective therapies. To explore if the persistence of systemic inflammation is associated with poor clinical outcomes in COPD we assessed patients recruited to the well-characterized ECLIPSE cohort (NCT00292552).&lt;h4>Methods and findings&lt;/h4>Six inflammatory biomarkers in peripheral blood (white blood cells (WBC) count and CRP, IL-6, IL-8, fibrinogen and TNF-α levels) were quantified in 1,755 COPD patients, 297 smokers with normal spirometry and 202 non-smoker controls that were followed-up for three years. We found that, at baseline, 30% of COPD patients did not show evidence of systemic inflammation whereas 16% h</pubmed_abstract><journal>PloS one</journal><pubmed_title>Persistent systemic inflammation is associated with poor clinical outcomes in COPD: a novel phenotype.</pubmed_title><pmcid>PMC3356313</pmcid><funding_grant_id>G0901786</funding_grant_id><funding_grant_id>G0901697</funding_grant_id><pubmed_authors>Wouters E</pubmed_authors><pubmed_authors>Bakke P</pubmed_authors><pubmed_authors>Wise R</pubmed_authors><pubmed_authors>Yates J</pubmed_authors><pubmed_authors>Ivanov Y</pubmed_authors><pubmed_authors>Silverman E</pubmed_authors><pubmed_authors>Killian K</pubmed_authors><pubmed_authors>Greenwald G</pubmed_authors><pubmed_authors>Wanner A</pubmed_authors><pubmed_authors>Krepelka J</pubmed_authors><pubmed_authors>Sharafkhaneh A</pubmed_authors><pubmed_authors>Kostov K</pubmed_authors><pubmed_authors>Crim C</pubmed_authors><pubmed_authors>Fitzgerald M</pubmed_authors><pubmed_authors>Rennard S</pubmed_authors><pubmed_authors>Sauleda J</pubmed_authors><pubmed_authors>Casaburi R</pubmed_authors><pubmed_authors>Yates JC</pubmed_authors><pubmed_authors>Siler T</pubmed_authors><pubmed_authors>Schuller D</pubmed_authors><pubmed_authors>Tal-Singer R</pubmed_authors><pubmed_authors>Feschenko Y</pubmed_authors><pubmed_authors>ZuWallack R</pubmed_authors><pubmed_authors>Edwards L</pubmed_authors><pubmed_authors>Edwards LD</pubmed_authors><pubmed_authors>Sciurba F</pubmed_authors><pubmed_authors>Celli B</pubmed_authors><pubmed_authors>MacNee W</pubmed_authors><pubmed_authors>Levy R</pubmed_authors><pubmed_authors>Agusti A</pubmed_authors><pubmed_authors>Giessel G</pubmed_authors><pubmed_authors>Anzueto A</pubmed_authors><pubmed_authors>Coxson HO</pubmed_authors><pubmed_authors>Silverman EK</pubmed_authors><pubmed_authors>Mayer RJ</pubmed_authors><pubmed_authors>Yashina L</pubmed_authors><pubmed_authors>Mahler D</pubmed_authors><pubmed_authors>Make B</pubmed_authors><pubmed_authors>Coxson H</pubmed_authors><pubmed_authors>Miller B</pubmed_authors><pubmed_authors>Scanlon P</pubmed_authors><pubmed_authors>Kosnik M</pubmed_authors><pubmed_authors>Bourbeau J</pubmed_authors><pubmed_authors>Hernandez P</pubmed_authors><pubmed_authors>Hanania N</pubmed_authors><pubmed_authors>Calverley P</pubmed_authors><pubmed_authors>Singh D</pubmed_authors><pubmed_authors>Calverley PM</pubmed_authors><pubmed_authors>Vestbo J</pubmed_authors><pubmed_authors>Gotfried M</pubmed_authors><pubmed_authors>O'Donnell D</pubmed_authors><pubmed_authors>Lomas D</pubmed_authors><pubmed_authors>Quinn D</pubmed_authors><pubmed_authors>Wedzicha J</pubmed_authors><pubmed_authors>Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE) Investigators</pubmed_authors><pubmed_authors>Maltais F</pubmed_authors><pubmed_authors>Rennard SI</pubmed_authors><pubmed_authors>Lomas DA</pubmed_authors><pubmed_authors>Miller BE</pubmed_authors><pubmed_authors>Gavrisyuk V</pubmed_authors><pubmed_authors>Braman S</pubmed_authors><pubmed_authors>Rochester C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Persistent systemic inflammation is associated with poor clinical outcomes in COPD: a novel phenotype.</name><description>&lt;h4>Background&lt;/h4>Because chronic obstructive pulmonary disease (COPD) is a heterogeneous condition, the identification of specific clinical phenotypes is key to developing more effective therapies. To explore if the persistence of systemic inflammation is associated with poor clinical outcomes in COPD we assessed patients recruited to the well-characterized ECLIPSE cohort (NCT00292552).&lt;h4>Methods and findings&lt;/h4>Six inflammatory biomarkers in peripheral blood (white blood cells (WBC) count and CRP, IL-6, IL-8, fibrinogen and TNF-α levels) were quantified in 1,755 COPD patients, 297 smokers with normal spirometry and 202 non-smoker controls that were followed-up for three years. We found that, at baseline, 30% of COPD patients did not show evidence of systemic inflammation whereas 16% h</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012</publication><modification>2026-04-29T16:28:18.072Z</modification><creation>2026-04-07T15:21:11.764Z</creation></dates><accession>S-EPMC3356313</accession><cross_references><pubmed>22624038</pubmed><doi>10.1371/journal.pone.0037483</doi></cross_references></HashMap>