Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/46588
Title: | The Fcγ receptor IIA-H/H131 genotype is associated with bacteremia in pneumococcal community-acquired pneumonia | Authors: | Solé-Violán, Jordi García-Laorden, M. Isabel Marcos-Ramos, José Alberto Rodríguez De Castro, Felipe Rajas, Olga Borderías, Luis Briones, M. Luisa Herrera-Ramos, Estefanía Blanquer, José Aspa, Javier Florido, Yanira García-Bello, Miguel Angel Ferrer-Agüero, José María Sologuren, Ithaisa Rodriguez-Gallego, Carlos |
UNESCO Clasification: | 32 Ciencias médicas 320508 Enfermedades pulmonares 320505 Enfermedades infecciosas |
Keywords: | C-Reactive Protein Mannose-Binding Lectin Streptococcus-Pneumoniae Igg Subclasses Capsular Polysaccharide, et al |
Issue Date: | 2011 | Journal: | Critical Care Medicine | Abstract: | Objective: To assess the potential association of the functional polymorphism rs1801274 in the receptor IIa for the Fc portion of immunoglobin G (Fc gamma RIIa) gene (FCGR2A-H131R) with the susceptibility to and the severity of community-acquired pneumonia (CAP).Design: Multicenter prospective and observational study.Setting: Four university hospitals in Spain.Patients: FCGR2A-H131R polymorphism was determined in 1,262 patients with CAP and in 1,224 in the subject control group.Measurements and Main Results: Severe sepsis was recorded in 366 patients. No significant differences in genotype or allele frequencies were seen among patients with CAP or pneumococcal CAP (PCAP) and controls. Patients with bacteremic PCAP (B-PCAP) had significantly higher frequencies of FCGR2A-H/H131 genotypes than those with nonbacteremic PCAP (p = .00016, odds ratio = 2.9, 95% confidence interval 1.58-5.3). The differences remained significant when adjusting for pneumonia severity index, hospital of origin, and intensive care unit admission (p = .0012, odds ratio = 2.83, 95% confidence interval 1.51-5.32). B-PCAP was associated with a significantly higher severity of the disease, evaluated as sepsis severity (p = .000007, odds ratio = 4.40, 95% confidence interval 2.31-8.39), multiorgan dysfunction syndrome (0.00048, odds ratio = 3.29, 95% confidence interval 1.69-6.41), intensive care unit admission, acute renal failure, and acute respiratory distress syndrome.Conclusions: Our results do not support a role of FCGR2A-H131R polymorphism in susceptibility to CAP or PCAP. However, we provide the insight that homozygosity for FCGR2A-H131 predisposes B-PCAP, which was associated with higher severity in our study. | URI: | http://hdl.handle.net/10553/46588 | ISSN: | 0090-3493 | DOI: | 10.1097/CCM.0b013e31820eda74 | Source: | Critical Care Medicine[ISSN 0090-3493],v. 39, p. 1388-1393 |
Appears in Collections: | Artículos |
Items in accedaCRIS are protected by copyright, with all rights reserved, unless otherwise indicated.