Department of Respiratory Medicine, Beijing Friendship Hospital, Capital Medical University, Beijing, People's Republic of China.
Respir Care. 2013 Apr;58(4):655-61. doi: 10.4187/respcare.01827.
Plasma level of human β-defensin 2 (HBD-2), noted to play a role in lung inflammatory diseases, is elevated in patients with pneumonia.
To investigate the prognostic value of plasma HBD-2 concentration in predicting 30-day clinical outcomes in patients with community-acquired pneumonia (CAP).
Patients with CAP were divided into 2 groups, based on the 30-day clinical outcomes, presence or absence of adverse outcomes (death, need for invasive mechanical ventilation, development of new complication of pneumonia). Demographic data, comorbidities, baseline clinical and laboratory features, plasma HBD-2 concentration, and the CURB-65 (confusion, urea nitrogen, breathing frequency, blood pressure, ≥ 65 years of age) scores on admission were compared between the 2 groups in univariable analysis. Multivariable logistic regression was used to test the predictor of adverse outcomes. Receiver operating characteristic analyses were used to calculate the power of the assays to predict the 30-day adverse outcomes.
We enrolled 361 subjects with CAP between March 2007 and March 2011. Univariate analysis revealed the following as predictive factors: age, smoking status, duration from symptom onset to admission, bilateral radiographic changes, total white-blood-cell count, serum sodium, serum potassium, serum albumin, plasma HBD-2 concentration, CURB-65 score, and comorbidities. In the multivariable logistic regression, plasma HBD-2 concentration, CURB-65 score, and age were independent predictors of 30-day adverse outcomes. In the receiver operating characteristic analysis, plasma HBD-2 concentration had an area under the curve of 0.77 (95% CI 0.71-0.82); the optimal cutoff point was 12.5 mg/L (sensitivity of 63%, specificity of 84%, positive predictive value of 42%, and negative predictive value of 88%), which predicted 30-day adverse outcomes in subjects with CAP.
In CAP patients, plasma HBD-2 level on admission is associated with 30-day clinical outcomes, and lower plasma HBD-2 level is an independent predictor for adverse outcomes. Plasma HBD-2 level may become a useful tool for prognostic stratification in patients with CAP.
人β防御素 2(HBD-2)的血浆水平在肺部炎症性疾病中起作用,在肺炎患者中升高。
探讨血浆 HBD-2 浓度预测社区获得性肺炎(CAP)患者 30 天临床结局的预后价值。
根据 30 天临床结局,将 CAP 患者分为存在或不存在不良结局(死亡、需要有创机械通气、肺炎新并发症发展)两组。在单变量分析中比较两组间人口统计学数据、合并症、基线临床和实验室特征、血浆 HBD-2 浓度和入院时 CURB-65(意识障碍、尿素氮、呼吸频率、血压、年龄≥65 岁)评分。多变量逻辑回归用于检验不良结局的预测因子。接收者操作特征分析用于计算检测预测 30 天不良结局的能力。
我们于 2007 年 3 月至 2011 年 3 月间纳入 361 例 CAP 患者。单变量分析显示以下因素为预测因子:年龄、吸烟状况、从症状发作到入院的时间、双侧放射学改变、白细胞总数、血清钠、血清钾、血清白蛋白、血浆 HBD-2 浓度、CURB-65 评分和合并症。多变量逻辑回归显示,血浆 HBD-2 浓度、CURB-65 评分和年龄是 30 天不良结局的独立预测因子。在接收者操作特征分析中,血浆 HBD-2 浓度的曲线下面积为 0.77(95%CI 0.71-0.82);最佳截断点为 12.5mg/L(敏感性 63%、特异性 84%、阳性预测值 42%、阴性预测值 88%),可预测 CAP 患者 30 天不良结局。
在 CAP 患者中,入院时的血浆 HBD-2 水平与 30 天临床结局相关,较低的血浆 HBD-2 水平是不良结局的独立预测因子。血浆 HBD-2 水平可能成为 CAP 患者预后分层的有用工具。