Preinfection systemic inflammatory markers and risk of hospitalization due to pneumonia

被引:117
作者
Yende, S
Tuomanen, EI
Wunderink, R
Kanaya, A
Newman, AB
Harris, T
Rekeneire, NC
Kritchevsky, SB
机构
[1] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Crit Care Med, CRISMA Lab, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA 15261 USA
[3] St Jude Childrens Res Hosp, Dept Infect Dis, Memphis, TN 38105 USA
[4] Northwestern Univ, Feinberg Sch Med, Div Pulm & Crit Care Med, Chicago, IL 60611 USA
[5] Univ Calif San Francisco, Div Gen Internal Med, San Francisco, CA 94143 USA
[6] NIA, Lab Epidemiol Demog & Biometry, Bethesda, MD 20892 USA
[7] Wake Forest Univ, Sch Med, Sticht Ctr Aging, Winston Salem, NC 27109 USA
关键词
inflammatory markers; interleukin; 6; tumor necrosis factor; pneumonia; TUMOR-NECROSIS-FACTOR; COMMUNITY-ACQUIRED PNEUMONIA; FACTOR-ALPHA; PNEUMOCOCCAL PNEUMONIA; HOST-DEFENSE; IN-VITRO; RECEPTOR; INTERLEUKIN-6; DISEASE; LUNG;
D O I
10.1164/rccm.200506-888OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Elevated proinflammatory cytokines are associated with severity of pneumonia, but the role of preinfection cytokine levels in the predisposition to pneumonia in humans is less clear. Objective: To ascertain role of preinfection inflammatory markers on susceptibility to community-acquired pneumonia (CAP). Methods: Longitudinal analysis over 6.5 yr of a cohort that consisted of 70- to 79-yr-old well-functioning elderly individuals. Measurements: Association between preinfection tumor necrosis factor (TNF), interleukin 6 (IL-6), and C-reactive protein (CIRP) levels and CAP requiring hospitalization. Results: Of the 3,075 participants, 161 (5.2%) developed at least one episode of CAP requiring hospitalization over a median duration of 3.3 yr. The highest tertiles of TNF (> 3.7 pg/ml) and IL-6 (> 2.4 pg/ml) were associated with increased risk of CAP, and the adjusted odds ratios were 1.6 (95% confidence interval [CI], 1.02-2.7) and 1.7 (95% CI, 1.1-2.8), respectively. The adjusted risk of CAP with at least one of these markers in the highest tertile was 1.6 (95% CI, 1.1-2.3). TNF and IL-6 levels in the highest tertile had a synergistic effect (p = 0.01 for interaction), and risk of CAP for both markers in the highest tertile was 2.8 (95% CI, 1.8-4.3). An FEV1 of 50% or less of predicted was associated with the highest risk of CAP (adjusted odds ratio, 3.6; 95% CI, 2.3-5.6). Furthermore, TNF and IL-6 levels modified risk of CAP in participants with coexisting medical conditions and history of smoking. Conclusion: In the well-functioning elderly subjects, preinfection systemic levels of TNF and IL-6 were associated with higher risk of CAP requiring hospitalization in smokers and those with coexisting medical conditions.
引用
收藏
页码:1440 / 1446
页数:7
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