Por favor, use este identificador para citar o enlazar este ítem:http://uvadoc.uva.es/handle/10324/45478
Título
Association of CD14 rs2569190 polymorphism with mortality in shock septic patients who underwent major cardiac or abdominal surgery: A retrospective study
Autor
Año del Documento
2018
Editorial
Springer Nature
Descripción
Producción Científica
Documento Fuente
Scientific Reports, 2018, vol. 8. 8 p.
Resumo
The aim of this study was to investigate the relationship between the CD14 rs2569190 polymorphism and death related to septic shock in white European patients who underwent major cardiac or abdominal surgery. We carried out a retrospective study in 205 septic shock patients. The septic shock diagnosis was established by international consensus definitions. The outcome variable was the death within 28, 60 and 90 days after septic shock diagnosis. The CD14 rs2569190 polymorphism was analyzed by Agena Bioscience’s MassARRAY platform. For the genetic association analysis with survival was selected a recessive inheritance model (GG vs. AA/AG). One hundred thirteen out of 205 patients (55.1%) died with a survival median of 39 days (95%CI = 30.6; 47.4). Patients with rs2569190 GG genotype had shorter survival probability than rs2569190 AA/AG genotype at 60 days (62.3% vs 50%; p = 0.035), and 90 days (62.3% vs 52.6%; p = 0.046). The rs2569190 GG genotype was associated with increased risk of septic shock-related death in the first 60 days (adjusted hazard ratio (aHR) = 1.67; p = 0.016) and 90 days (aHR = 1.64; p = 0.020) compared to rs2569190 AA/AG genotype. In conclusion, the presence of CD14 rs2569190 GG genotype was associated with death in shock septic patients who underwent major surgery. Further studies with bigger sample size are required to verify this relationship.
Materias Unesco
3213.01 Cirugía Abdominal
3213.07 Cirugía del Corazón
Palabras Clave
Polymorphism
Polimorfismo
Mortality
Mortalidad
Septic shock
Choque séptico
ISSN
2045-2322
Revisión por pares
SI
Patrocinador
Centro Nacional de Genotipado (grant CEGEN-PRB2-ISCIII)
Instituto de Salud Carlos III (grants PT13/0001, PI15/01451, CD13/00013, CD14/00002 and CP14CIII/00010)
Junta de Castilla y Leon (grants GR463/A/10 and GR773/A/13)
PFIZER (grant CT25-ESP01-01)
Instituto de Salud Carlos III (grants PT13/0001, PI15/01451, CD13/00013, CD14/00002 and CP14CIII/00010)
Junta de Castilla y Leon (grants GR463/A/10 and GR773/A/13)
PFIZER (grant CT25-ESP01-01)
Version del Editor
Propietario de los Derechos
© 2018 Springer Nature
Idioma
eng
Tipo de versión
info:eu-repo/semantics/publishedVersion
Derechos
openAccess
Aparece en las colecciones
Arquivos deste item
Exceto quando indicado o contrário, a licença deste item é descrito como Attribution-NonCommercial-NoDerivatives 4.0 Internacional