Adamzik Michael, Frey Ulrich H, Rieman Kathrin, Sixt Stephan, Beiderlinden Martin, Siffert Winfried, Peters Jürgen
Institut für Pharmakogenetik, University Hospital Essen, University of Duisburg-Essen, Hufelandstrasse 55, 45147, Essen, Germany.
Klinik für Anästhesiologie und Intensivmedizin, University Hospital Essen, University of Duisburg-Essen, Hufelandstrasse 55, 45147, Essen, Germany.
Intensive Care Med. 2007 Jul;33(7):1199-1203. doi: 10.1007/s00134-007-0649-4. Epub 2007 Apr 28.
This study investigated whether the insertion/deletion polymorphism in the promoter of NFKB1 is associated with severity and/or mortality in ARDS.
Prospective study in a mixed anesthesiological ICU of the University Hospital Essen.
103 adult patients with ARDS (white Germans).
Patients with ARDS were genotyped for the insertion/deletion polymorphism in the promoter of NFKB1 (-94ins/delATTG). In ARDS patients genotypes differed significantly between those with severe ARDS [Lung Injury Score (LIS)>or=3; 23 homozygote deletion (DD), heterozygote (ID) 31, and homozygote insertion wildtype (II) 23], and those with LIS below 3 (1 DD, 9 ID, 16 II). Likewise, the frequency of the D allele was significantly less in patients with higher LIS (50% D) than lower LIS (21% D). Using these values produces a significantly higher OR of 16.0 (95% CI 1.96-130.9) for DD than for II, while the OR for ID vs. II was 2.4 (95% CI 0.9-6.4). Genotypes of the NFKB1 promoter polymorphism were associated neither with 30-day survival nor with duration of ICU stay.
The insertion/deletion polymorphism in the promoter of NFKB1 influences the severity but not the mortality of ARDS.
本研究调查了NFKB1启动子的插入/缺失多态性是否与急性呼吸窘迫综合征(ARDS)的严重程度和/或死亡率相关。
在埃森大学医院的混合麻醉重症监护病房进行的前瞻性研究。
103例成年ARDS患者(德国白人)。
对ARDS患者进行NFKB1启动子插入/缺失多态性(-94ins/delATTG)基因分型。在ARDS患者中,重度ARDS患者[肺损伤评分(LIS)≥3;23例纯合子缺失(DD)、31例杂合子(ID)和23例纯合子插入野生型(II)]与LIS低于3的患者(1例DD、9例ID、16例II)的基因型存在显著差异。同样,LIS较高的患者(D等位基因频率为50%)的D等位基因频率显著低于LIS较低的患者(D等位基因频率为21%)。使用这些值得出,DD型患者的优势比(OR)显著高于II型患者,为16.0(95%置信区间1.96 - 130.9),而ID型与II型相比的OR为2.4(95%置信区间0.9 - 6.4)。NFKB1启动子多态性的基因型与30天生存率和重症监护病房住院时间均无关。
NFKB1启动子的插入/缺失多态性影响ARDS的严重程度,但不影响其死亡率。