<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(1)</volume><submitter>Jabandziev P</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The aim of the study was to identify the dependency structure of genetic variants that can influence the outcome for paediatric patients with sepsis.&lt;h4>Methods&lt;/h4>We evaluated the role of single nucleotide polymorphisms for five genes: bactericidal permeability increasing protein (BPI; rs5743507), lipopolysaccharide-binding protein (LBP; rs2232618), toll-like receptor 4 (TLR4; rs4986790), heat shock protein 70 (HSP 70; rs2227956), and interleukin 6 (IL-6; rs1800795) in 598 children aged 0 to 19 years that were admitted to a paediatric intensive care unit with fever, systemic inflammatory response syndrome, sepsis, severe sepsis, septic shock, or multiple organ dysfunction syndrome. A control group of 529 healthy individuals was included. Multi-way contingency tables </pubmed_abstract><journal>Critical care (London, England)</journal><pagination>R1</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4056441</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Multiple gene-to-gene interactions in children with sepsis: a combination of five gene variants predicts outcome of life-threatening sepsis.</pubmed_title><pmcid>PMC4056441</pmcid><pubmed_authors>Michalek J</pubmed_authors><pubmed_authors>Smerek M</pubmed_authors><pubmed_authors>Hubacek JA</pubmed_authors><pubmed_authors>Fedora M</pubmed_authors><pubmed_authors>Kosinova L</pubmed_authors><pubmed_authors>Jabandziev P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multiple gene-to-gene interactions in children with sepsis: a combination of five gene variants predicts outcome of life-threatening sepsis.</name><description>&lt;h4>Introduction&lt;/h4>The aim of the study was to identify the dependency structure of genetic variants that can influence the outcome for paediatric patients with sepsis.&lt;h4>Methods&lt;/h4>We evaluated the role of single nucleotide polymorphisms for five genes: bactericidal permeability increasing protein (BPI; rs5743507), lipopolysaccharide-binding protein (LBP; rs2232618), toll-like receptor 4 (TLR4; rs4986790), heat shock protein 70 (HSP 70; rs2227956), and interleukin 6 (IL-6; rs1800795) in 598 children aged 0 to 19 years that were admitted to a paediatric intensive care unit with fever, systemic inflammatory response syndrome, sepsis, severe sepsis, septic shock, or multiple organ dysfunction syndrome. A control group of 529 healthy individuals was included. Multi-way contingency tables </description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jan</publication><modification>2026-04-29T16:20:12.204Z</modification><creation>2026-04-07T15:21:05.574Z</creation></dates><accession>S-EPMC4056441</accession><cross_references><pubmed>24383711</pubmed><doi>10.1186/cc13174</doi></cross_references></HashMap>