Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study. Issue 1 (January 2015)

• Record Type: Journal Article
• Authors: Rautanen, Anna; Mills, Tara C; Gordon, Anthony C; Hutton, Paula; Steffens, Michael; Nuamah, Rosamond; Chiche, Jean-Daniel; Parks, Tom; Chapman, Stephen J; Davenport, Emma E; Elliott, Katherine S; Bion, Julian; Lichtner, Peter; Meitinger, Thomas; Wienker, Thomas F; Caulfield, Mark J; Mein, Charles; Bloos, Frank; Bobek, Ilona; Cotogni, Paolo; Sramek, Vladimir; Sarapuu, Silver; Kobilay, Makbule; Ranieri, V Marco; Rello, Jordi; Sirgo, Gonzalo; Weiss, Yoram G; Russwurm, Stefan; Schneider, E Marion; Reinhart, Konrad; Holloway, Paul A H; Knight, Julian C; Garrard, Chris S; Russell, James A; Walley, Keith R; Stüber, Frank; Hill, Adrian V S; Hinds, Charles J; for the ESICM/ECCRN GenOSept Investigators;
• Is Part Of: Lancet. Volume 3:Issue 1(2015)
• Page Start: 53
• Page End: 60
• Publication Date: 2015-01
• Subjects: Respiratory organs -- Diseases -- Periodicals; 616.2005
• DOI: 10.1016/S2213-2600(14)70290-5
• Languages: English
• ISSNs: 2213-2600

Abstract

<abstract abstract-type="author" id="ceab10"> <title id="cestitle10">Summary</title> <sec> <title id="cestitle20">Background</title> <p id="spara140">Sepsis continues to be a major cause of death, disability, and health-care expenditure worldwide. Despite evidence suggesting that host genetics can influence sepsis outcomes, no specific loci have yet been convincingly replicated. The aim of this study was to identify genetic variants that influence sepsis survival.</p> </sec> <sec> <title id="cestitle30">Methods</title> <p id="spara150">We did a genome-wide association study in three independent cohorts of white adult patients admitted to intensive care units with sepsis, severe sepsis, or septic shock (as defined by the International Consensus Criteria) due to pneumonia or intra-abdominal infection (cohorts 1–3, n=2534 patients). The primary outcome was 28 day survival. Results for the cohort of patients with sepsis due to pneumonia were combined in a meta-analysis of 1553 patients from all three cohorts, of whom 359 died within 28 days of admission to the intensive-care unit. The most significantly associated single nucleotide polymorphisms (SNPs) were genotyped in a further 538 white patients with sepsis due to pneumonia (cohort 4), of whom 106 died.</p> </sec> <sec> <title id="cestitle40">Findings</title> <p id="spara160">In the genome-wide meta-analysis of three independent pneumonia cohorts (cohorts 1–3), common variants in the <italic>FER</italic> gene were strongly associated with survival (p=9·7 × 10<sup>−8</sup>). Further genotyping of the top associated SNP (rs4957796) in the additional cohort (cohort 4) resulted in a combined p value of 5·6 × 10<sup>−8</sup> (odds ratio 0·56, 95% CI 0·45–0·69). In a time-to-event analysis, each allele reduced the mortality over 28 days by 44% (hazard ratio for death 0·56, 95% CI 0·45–0·69; likelihood ratio test p=3·4 × 10<sup>−9</sup>, after adjustment for age and stratification by cohort). Mortality was 9·5% in patients carrying the CC genotype, 15·2% in those carrying the TC genotype, and 25·3% in those carrying the TT genotype. No significant genetic associations were identified when patients with sepsis due to pneumonia and intra-abdominal infection were combined.</p> </sec> <sec> <title id="cestitle50">Interpretation</title> <p id="spara170">We have identified common variants in the <italic>FER</italic> gene that associate with a reduced risk of death from sepsis due to pneumonia. The <italic>FER</italic> gene and associated molecular pathways are potential novel targets for therapy or prevention and candidates for the development of biomarkers for risk stratification.</p> </sec> <sec> <title id="cestitle60">Funding</title> <p id="spara180">European Commission and the Wellcome Trust.</p> </sec> </abstract>