<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Egli A</submitter><funding>Nachwuchsförderung</funding><funding>Swiss National Science Foundation</funding><pagination>51</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5861655</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Interferon lambdas (IFNLs) have important anti-viral/bacterial and immunomodulatory functions in the respiratory tract. How do IFNLs impact COPD and its exacerbations?&lt;h4>Methods&lt;/h4>Five hundred twenty eight patients were recruited in a prospective observational multicentre cohort (PROMISE) study. The genetic polymorphisms (rs8099917 and rs12979860) within the IFNL3/4 gene region and circulating levels of IFNL3 in COPD patients were determined and associated with disease activity and outcome during a median follow-up of 24 months.&lt;h4>Results&lt;/h4>The GG genotype significantly influenced severe exacerbation rate (42 vs. 23%; p = 0.032) and time to severe exacerbation (HR = 2.260; p = 0.012). Compared to the TT or TG genotypes, the GG genotype was associated with severe dy</pubmed_abstract><journal>BMC pulmonary medicine</journal><pubmed_title>IFNΛ3/4 locus polymorphisms and IFNΛ3 circulating levels are associated with COPD severity and outcomes.</pubmed_title><pmcid>PMC5861655</pmcid><funding_grant_id>154709</funding_grant_id><funding_grant_id>PZ00P3_154709/1</funding_grant_id><funding_grant_id>128412</funding_grant_id><funding_grant_id>PP00P3_128412/1</funding_grant_id><pubmed_authors>Blasi F</pubmed_authors><pubmed_authors>Roth M</pubmed_authors><pubmed_authors>Lacoma A</pubmed_authors><pubmed_authors>Thomas B</pubmed_authors><pubmed_authors>Mandal J</pubmed_authors><pubmed_authors>Stolz D</pubmed_authors><pubmed_authors>Boersma W</pubmed_authors><pubmed_authors>Schumann DM</pubmed_authors><pubmed_authors>Louis R</pubmed_authors><pubmed_authors>Kostikas K</pubmed_authors><pubmed_authors>Rentsch K</pubmed_authors><pubmed_authors>Aerts JG</pubmed_authors><pubmed_authors>Lorne Tyrrell D</pubmed_authors><pubmed_authors>Milenkovic B</pubmed_authors><pubmed_authors>Rohde GGU</pubmed_authors><pubmed_authors>Tamm M</pubmed_authors><pubmed_authors>Egli A</pubmed_authors><pubmed_authors>Welte T</pubmed_authors><pubmed_authors>Torres A</pubmed_authors></additional><is_claimable>false</is_claimable><name>IFNΛ3/4 locus polymorphisms and IFNΛ3 circulating levels are associated with COPD severity and outcomes.</name><description>&lt;h4>Background&lt;/h4>Interferon lambdas (IFNLs) have important anti-viral/bacterial and immunomodulatory functions in the respiratory tract. How do IFNLs impact COPD and its exacerbations?&lt;h4>Methods&lt;/h4>Five hundred twenty eight patients were recruited in a prospective observational multicentre cohort (PROMISE) study. The genetic polymorphisms (rs8099917 and rs12979860) within the IFNL3/4 gene region and circulating levels of IFNL3 in COPD patients were determined and associated with disease activity and outcome during a median follow-up of 24 months.&lt;h4>Results&lt;/h4>The GG genotype significantly influenced severe exacerbation rate (42 vs. 23%; p = 0.032) and time to severe exacerbation (HR = 2.260; p = 0.012). Compared to the TT or TG genotypes, the GG genotype was associated with severe dy</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Mar</publication><modification>2025-04-18T23:39:25.024Z</modification><creation>2019-06-06T19:10:11Z</creation></dates><accession>S-EPMC5861655</accession><cross_references><pubmed>29562888</pubmed><doi>10.1186/s12890-018-0616-6</doi></cross_references></HashMap>