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http://purl.uniprot.org/citations/29334679http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/29334679http://www.w3.org/2000/01/rdf-schema#comment"

Background

The IL10 family of genes includes crucial immune regulators. We tested the hypothesis that single nucleotide polymorphisms (SNPs) in IL10, IL19, IL20, and IL24 of the IL10 family gene cluster alter the clinical outcome of septic shock.

Methods

Patients with septic shock (n = 1,193) were genotyped for 13 tag SNPs of IL10, IL19, IL20, and IL24. IL20 gene expression was measured in genotyped lymphoblastoid cells in vitro. Cardiac surgical ICU patients (n = 981) were genotyped for IL20 rs2981573 A/G. The primary outcome variable was 28-day mortality.

Results

Patients with the G allele of IL20 rs2981573 had a significantly increased hazard of death over the 28-day period compared to patients with the A allele in the septic shock cohort (adjusted hazard ratio 1.27; 95% confidence interval 1.10-1.47; p = 8.0 × 10-4). Patients with the GG genotype had more organ dysfunction (p < 0.05). The GG genotype was associated with increased IL20 gene expression in stimulated lymphoblastoid cells in vitro (p < 0.05). The cardiac surgical ICU patients with the GG genotype had an increased length of ICU stay (p = 0.032).

Conclusions

The GG genotype of IL20 rs2981573 SNP was associated with increased IL20 gene expression and increased adverse outcomes in patients with septic shock and following cardiac surgery."xsd:string
http://purl.uniprot.org/citations/29334679http://purl.org/dc/terms/identifier"doi:10.1159/000486104"xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/author"Shimada T."xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/author"Boyd J.H."xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/author"Walley K.R."xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/author"Russell J.A."xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/author"Nakada T.A."xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/author"Nakada E."xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/author"Thair S.A."xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/author"Wacharasint P."xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/date"2018"xsd:gYear
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/name"J Innate Immun"xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/pages"181-188"xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/title"The IL20 Genetic Polymorphism Is Associated with Altered Clinical Outcome in Septic Shock."xsd:string
http://purl.uniprot.org/citations/29334679http://purl.uniprot.org/core/volume"10"xsd:string
http://purl.uniprot.org/citations/29334679http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/29334679
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