4G/5G Polymorphism of Plasminogen Activator Inhibitor-1 Gene Is Associated with Mortality in Intensive Care Unit Patients with Severe Pneumonia

被引:30
作者
Sapru, Anil [1 ]
Hansen, Helen [3 ]
Ajayi, Temitayo
Brown, Ron [2 ]
Garcia, Oscar [2 ]
Zhuo, HanJing [2 ]
Wiemels, Joseph [3 ]
Matthay, Michael A. [2 ,4 ]
Wiener-Kronish, Jeanine [5 ]
机构
[1] Univ Calif San Francisco, Div Crit Care Med, Dept Pediat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med & Anesthesia, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Mol Epidemiol Lab, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[5] Massachusetts Gen Hosp, Dept Anesthesia & Crit Care, Boston, MA 02114 USA
关键词
RESPIRATORY-DISTRESS-SYNDROME; COMMUNITY-ACQUIRED PNEUMONIA; UROKINASE RECEPTOR; LOCAL ACTIVATION; FIBRIN TURNOVER; TISSUE FACTOR; LUNG-DISEASE; COAGULATION; GUIDELINES; PROMOTER;
D O I
10.1097/ALN.0b013e3181a1081d
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Higher plasma and pulmonary edema fluid levels of plasminogen activator inhibitor-1 (PAI-1) are associated with increased mortality in patients with pneumonia and acute lung injury. The 4G allele of the 4G/5G polymorphism of the PAI-1 gene is associated with higher PAI-1 levels and an increased incidence of hospitalizations for pneumonia. The authors hypothesized that the 4G allele would be associated with worse clinical outcomes (mortality and ventilator-free days) in patients with severe pneumonia. Methods: The authors enrolled patients admitted with severe pneumonia in a prospective cohort. Patients were followed until hospital discharge. DNA was isolated from blood samples, and genotyping detection for the PAI-1 4G/5G polymorphism was carried out using Taqman-based allelic discrimination. Results. A total of Ill patients were available for analysis. Distribution of genotypes was 4G/4G 26 of 111 (23%), 4G/5G 59 of 111 (53%), and 5G/5G 26 of 111 (23%). Of 111 patients, 32 (29%) died before hospital discharge and 105 patients (94%) received mechanical ventilation. Patients with the 4G/4G and the 4G/5G genotypes had higher mortality (35% vs. 8%, P = 0.007) and fewer ventilator-free days (median 4 vs. 13, P = 0.04) compared to patients with the 5G/5G genotype. Conclusions: The 4G allele of the 4G/5G polymorphism in the PAI-1 gene is associated with fewer ventilator-free days and increased mortality in hospitalized patients with severe pneumonia. These findings suggest that PAI-1 may have a role in pathogenesis and that the 4G/5G polymorphism may be an important biomarker of risk in patients with severe pneumonia.
引用
收藏
页码:1086 / 1091
页数:6
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