Harvard School of Public Health, 677 Huntington Avenue, Boston, MA 02115, USA.
Intensive Care Med. 2011 Jun;37(6):970-80. doi: 10.1007/s00134-011-2208-2. Epub 2011 Mar 11.
Excessive activation of the endothelium is associated with adverse outcomes in patients with systemic infections. Endothelium-associated peptides, such as endothelin-1 (ET-1), correlate closely with endothelial activation, and therefore serve as surrogate biomarkers. Our aim was to investigate precursor peptides of endothelin-1 (proET1) on admission and during follow-up on days 3, 5 and 7 in a prospective cohort of 925 patients with community-acquired pneumonia.
We investigated the association of initial and follow-up proET1 and other prohormone levels with 30-day mortality and ICU admission in proportional Cox regression models with time-varying covariates adjusted for the pneumonia-severity-index (PSI), and calculated reclassification statistics.
The mortality rate and ICU admission rate were 5.4% (95% CI 3.9-6.8%) and 9.0% (95% CI 7.1-10.8%). ProET1 levels on admission and changes from baseline to day 3 were significant mortality predictors with adjusted hazard ratios of 10.5 (95% CI 2.9-38.6) and 28.4 (95% CI 7.0-115.1). Initial proET1 levels improved the PSI in reclassification statistics (net reclassification improvement of 0.29, p<0.0001) and in c-statistics (from 0.79 to 0.83, p<0.01). Changes of proET1 on day 3 improved the c-statistic of the combined model of PSI and initial proET1 from 0.80 to 0.85 (p<0.01) and reclassification tables demonstrated a significant improvement (net reclassification improvement 0.44, p<0.0001). Similar significant results were found for the risk for ICU admission.
In community-acquired pneumonia, ET-1 precursor peptides on admission and changes from baseline to day 3 were independent predictors for mortality and ICU admission, and significantly improved the PSI. If verified in intervention studies, monitoring of proET1 may be helpful for endothelium targeting therapies and for risk stratification complementary to other prohormones.
内皮细胞过度激活与全身感染患者的不良预后相关。内皮细胞相关肽,如内皮素-1(ET-1),与内皮细胞激活密切相关,因此可作为替代生物标志物。我们的目的是在一项前瞻性队列研究中,调查 925 例社区获得性肺炎患者入院时和第 3、5 和 7 天的内皮素-1 前体肽(proET1)。
我们使用比例 Cox 回归模型,在时间变化的协变量中调整肺炎严重指数(PSI),调查初始和随访时 proET1 和其他前激素水平与 30 天死亡率和 ICU 入院的关系,并计算再分类统计数据。
死亡率和 ICU 入院率分别为 5.4%(95%CI 3.9-6.8%)和 9.0%(95%CI 7.1-10.8%)。入院时的 proET1 水平和从基线到第 3 天的变化是死亡的显著预测因子,调整后的危险比分别为 10.5(95%CI 2.9-38.6)和 28.4(95%CI 7.0-115.1)。初始 proET1 水平提高了 PSI 的再分类统计数据(净再分类改善 0.29,p<0.0001)和 C 统计量(从 0.79 提高到 0.83,p<0.01)。第 3 天 proET1 的变化提高了 PSI 和初始 proET1 联合模型的 C 统计量,从 0.80 提高到 0.85(p<0.01),再分类表显示出显著改善(净再分类改善 0.44,p<0.0001)。对于 ICU 入院的风险,也得到了类似的显著结果。
在社区获得性肺炎中,入院时和从基线到第 3 天的 ET-1 前体肽是死亡率和 ICU 入院的独立预测因子,并显著改善了 PSI。如果在干预研究中得到验证,proET1 的监测可能有助于内皮靶向治疗,并补充其他前激素进行风险分层。