Interleukin-1 receptor antagonist gene polymorphism and mortality in patients with severe sepsis

被引:86
作者
Arnalich, F
López-Maderuelo, D
Codoceo, R
Lopez, J
Solis-Garrido, LM
Capiscol, C
Fernandez-Capitán, C
Madero, R
Montiel, C
机构
[1] Univ Autonoma Madrid, Fac Med, Hosp La Paz, Dept Med, E-28049 Madrid, Spain
[2] Univ Autonoma Madrid, Fac Med, Hosp La Paz, Dept Pharmacol, E-28049 Madrid, Spain
[3] Univ Autonoma Madrid, Fac Med, Hosp La Paz, Dept Clin Biochem, E-28049 Madrid, Spain
[4] Univ Autonoma Madrid, Fac Med, Hosp La Paz, Intens Care Unit, E-28049 Madrid, Spain
关键词
interleukin-1Ra; gene polymorphism; cytokine production; peripheral blood; mononuclear cells; sepsis; outcome;
D O I
10.1046/j.1365-2249.2002.01743.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This study aims to determine the influence of the polymorphism within the intron 2 of the interleukin-1 receptor antagonist gene (IL-1RN*) on the outcome of severe sepsis, and to assess its functional significance by correlating this polymorphism with the total production of interleukin-1 receptor antagonist (IL-1Ra) protein determined in stimulated peripheral blood mononuclear cells (PBMC). A group of 78 patients with severe sepsis (51 survivors and 27 nonsurvivors) was compared with a healthy control group of 130 blood donors, and 56 patients with uncomplicated pneumonia. We found a significant association between IL-1RN* polymorphism and survival. Thus, after adjusting for age and APACHE II score, multiple logistic regression analysis showed that patients homozygotes for the allele *2 had a 6.47-fold increased risk of death (95% CI 1.01-41.47, P = 0.04). Besides, compared with patients homozygous or heterozygous for the allele *1, IL-1RN*2 homozygotes produced significantly lower levels of IL-1Ra from their PBMC. Our results suggest that insufficient production of this cytokine might contribute, among other factors, to the higher mortality rate found in severe sepsis patients with the IL-1RN*2 homozygous genotype.
引用
收藏
页码:331 / 336
页数:6
相关论文
共 23 条
[1]   Imbalance of the interleukin 1 system in colonic mucosa - association with intestinal inflammation and interleukin 1 receptor agonist genotype 2 [J].
Andus, T ;
Daig, R ;
Vogl, D ;
Aschenbrenner, E ;
Lock, G ;
Hollerbach, S ;
Kollinger, M ;
Scholmerich, J ;
Gross, V .
GUT, 1997, 41 (05) :651-657
[2]   CELL-MEDIATED IMMUNE-RESPONSE AND CYTOKINE PRODUCTION IN IDIOPATHIC SENILE ANOREXIA [J].
ARNALICH, F ;
HERNANZ, A ;
VAZQUEZ, JJ ;
AMORES, A .
MECHANISMS OF AGEING AND DEVELOPMENT, 1994, 77 (01) :67-74
[3]   Predictive value of nuclear factor κB activity and plasma cytokine levels in patients with sepsis [J].
Arnalich, F ;
Garcia-Palomero, E ;
López, J ;
Jiménez, M ;
Madero, R ;
Renart, J ;
Vazquez, JJ ;
Montiel, C .
INFECTION AND IMMUNITY, 2000, 68 (04) :1942-1945
[4]   Prediction of outcome from intensive care: A prospective cohort study comparing acute physiology and chronic health evaluation II and III prognostic systems in a United Kingdom intensive care unit [J].
Beck, DH ;
Taylor, BL ;
Millar, B ;
Smith, GB .
CRITICAL CARE MEDICINE, 1997, 25 (01) :9-15
[5]   INTERLEUKIN-1 RECEPTOR ANTAGONIST GENE POLYMORPHISM AS A DISEASE SEVERITY FACTOR IN SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
BLAKEMORE, AIF ;
TARLOW, JK ;
CORK, MJ ;
GORDON, C ;
EMERY, P ;
DUFF, GW .
ARTHRITIS AND RHEUMATISM, 1994, 37 (09) :1380-1385
[6]   DEFINITIONS FOR SEPSIS AND ORGAN FAILURE AND GUIDELINES FOR THE USE OF INNOVATIVE THERAPIES IN SEPSIS [J].
BONE, RC ;
BALK, RA ;
CERRA, FB ;
DELLINGER, RP ;
FEIN, AM ;
KNAUS, WA ;
SCHEIN, RMH ;
SIBBALD, WJ .
CHEST, 1992, 101 (06) :1644-1655
[7]   Association of the interleukin 1 receptor antagonist gene with ulcerative colitis in Northern European Caucasians [J].
Carter, MJ ;
di Giovine, FS ;
Jones, S ;
Mee, J ;
Camp, NJ ;
Lobo, AJ ;
Duff, GW .
GUT, 2001, 48 (04) :461-467
[8]  
Clay FE, 1996, HUM GENET, V97, P723
[9]  
DANIS VA, 1995, DIS MARKERS, V12, P135
[10]  
DANIS VA, 1995, CLIN EXP IMMUNOL, V99, P303