Adamzik Michael, Frey Ulrich H, Riemann Kathrin, Sixt Stephan, Lehmann Nils, Siffert Winfried, Peters Jürgen
Klinik für Anästhesiologie und Intensivmedizin, Universität Duisburg-Essen, Universitätsklinikum Essen, Essen, Germany.
Crit Care Med. 2008 Jun;36(6):1776-9. doi: 10.1097/CCM.0b013e318174373d.
Activation of coagulation and inflammation are parts of the innate host response to infection that may contribute to organ dysfunction and death when control of these systems is compromised. Thus, functional single nucleotide polymorphisms within candidate genes of the inflammation and coagulation cascade are possible factors which may influence severity and/or mortality in acute respiratory distress syndrome. The aim of this study was to investigate whether the factor V Leiden mutation (Arg506Gln) is associated with altered severity and/or mortality in acute respiratory distress syndrome.
Retrospective cohort, genetic association study.
Tertiary care intensive care unit.
Adults (white Germans) with acute respiratory distress syndrome (n = 106).
Genotyping for the factor V Leiden mutation.
Using Kaplan-Meier estimates to compare outcome, 30-day survival was significantly associated with the factor V Leiden mutation (p = .049). Thirty-day survival rates were 100% for Arg/Gln (n = 7) genotypes but only 58% for Arg/Arg (n = 99) genotypes, respectively.
We show for the first time that a heterozygous factor V Leiden genotype is associated with improved 30-day survival in patients with acute respiratory distress syndrome.
凝血和炎症激活是宿主对感染的固有反应的一部分,当这些系统的控制受到损害时,可能导致器官功能障碍和死亡。因此,炎症和凝血级联反应候选基因内的功能性单核苷酸多态性可能是影响急性呼吸窘迫综合征严重程度和/或死亡率的因素。本研究的目的是调查因子V莱顿突变(Arg506Gln)是否与急性呼吸窘迫综合征严重程度改变和/或死亡率相关。
回顾性队列基因关联研究。
三级医疗重症监护病房。
患有急性呼吸窘迫综合征的成年人(德国白人,n = 106)。
对因子V莱顿突变进行基因分型。
使用Kaplan-Meier估计值比较结果,30天生存率与因子V莱顿突变显著相关(p = 0.049)。Arg/Gln(n = 7)基因型的30天生存率为100%,而Arg/Arg(n = 99)基因型的30天生存率仅为58%。
我们首次表明,杂合子因子V莱顿基因型与急性呼吸窘迫综合征患者30天生存率提高相关。