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NFKB1基因启动子区域的插入/缺失多态性影响急性呼吸窘迫综合征的严重程度,但不影响其死亡率。

Insertion/deletion polymorphism in the promoter of NFKB1 influences severity but not mortality of acute respiratory distress syndrome.

作者信息

Adamzik Michael, Frey Ulrich H, Rieman Kathrin, Sixt Stephan, Beiderlinden Martin, Siffert Winfried, Peters Jürgen

机构信息

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.

出版信息

Intensive Care Med. 2007 Jul;33(7):1199-1203. doi: 10.1007/s00134-007-0649-4. Epub 2007 Apr 28.

Abstract

OBJECTIVE

This study investigated whether the insertion/deletion polymorphism in the promoter of NFKB1 is associated with severity and/or mortality in ARDS.

DESIGN AND SETTING

Prospective study in a mixed anesthesiological ICU of the University Hospital Essen.

PATIENTS AND PARTICIPANTS

103 adult patients with ARDS (white Germans).

MEASUREMENTS AND RESULTS

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.

CONCLUSIONS

The insertion/deletion polymorphism in the promoter of NFKB1 influences the severity but not the mortality of ARDS.

摘要

目的

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。

设计与背景

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。

患者与参与者

103例成年ARDS患者(德国白人)。

测量与结果

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。

结论

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。

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