Academic Respiratory Unit, University of Bristol, Bristol, UK
Bristol Centre for Antimicrobial Research, North Bristol NHS Trust, Bristol, UK.
Emerg Med J. 2021 Jul;38(7):543-548. doi: 10.1136/emermed-2020-210380. Epub 2021 May 21.
COVID-19 has an unpredictable clinical course, so prognostic biomarkers would be invaluable when triaging patients on admission to hospital. Many biomarkers have been suggested using large observational datasets but sample timing is crucial to ensure prognostic relevance. The DISCOVER study prospectively recruited patients with COVID-19 admitted to a UK hospital and analysed a panel of putative prognostic biomarkers on the admission blood sample to identify markers of poor outcome.
Consecutive patients admitted to hospital with proven or clinicoradiological suspected COVID-19 were consented. Admission bloods were extracted from the clinical laboratory. A panel of biomarkers (interleukin-6 (IL-6), soluble urokinase plasminogen activator receptor (suPAR), Krebs von den Lungen 6, troponin, ferritin, lactate dehydrogenase, B-type natriuretic peptide, procalcitonin) were performed in addition to routinely performed markers (C reactive protein (CRP), neutrophils, lymphocytes, neutrophil:lymphocyte ratio). Age, National Early Warning Score (NEWS2), CURB-65 and radiographic severity score on initial chest radiograph were included as comparators. All biomarkers were tested in logistic regression against a composite outcome of non-invasive ventilation, intensive care admission or death, with area under the curve (AUC) (figures calculated).
187 patients had 28-day outcomes at the time of analysis. CRP (AUC: 0.69, 95% CI: 0.59 to 0.78), lymphocyte count (AUC: 0.62, 95% CI: 0.53 to 0.72) and other routine markers did not predict the primary outcome. IL-6 (AUC: 0.77, 0.65 to 0.88) and suPAR (AUC: 0.81, 0.72 to 0.88) showed some promise, but simple clinical features alone such as NEWS2 score (AUC: 0.70, 0.60 to 0.79) or age (AUC: 0.70, 0.62 to 0.77) performed nearly as well.
Admission blood biomarkers have only moderate predictive value for predicting COVID-19 outcomes, while simple clinical features such as age and NEWS2 score outperform many biomarkers. IL-6 and suPAR had the best performance, and further studies should focus on the additive value of these biomarkers to routine care.
COVID-19 的临床病程不可预测,因此在将患者分诊至医院入院时,预后生物标志物将非常有价值。已经使用大型观察性数据集提出了许多生物标志物,但样本时间至关重要,以确保具有预后相关性。 DISCOVER 研究前瞻性地招募了在英国医院住院的 COVID-19 患者,并分析了入院血液样本中的一组推定预后生物标志物,以确定不良预后的标志物。
同意患有经证实或临床放射学疑似 COVID-19 的住院患者入组。从临床实验室提取入院血液。除了常规进行的标志物(C 反应蛋白(CRP)、中性粒细胞、淋巴细胞、中性粒细胞:淋巴细胞比值)外,还进行了一组生物标志物(白细胞介素 6(IL-6)、可溶性尿激酶型纤溶酶原激活物受体(suPAR)、Krebs von den Lungen 6、肌钙蛋白、铁蛋白、乳酸脱氢酶、B 型利钠肽、降钙素原)。年龄、早期预警评分 2(NEWS2)、CURB-65 和初始胸片上的放射严重程度评分被用作比较。所有生物标志物均在逻辑回归中针对无创通气、入住重症监护病房或死亡的综合结局进行测试,曲线下面积(AUC)(计算得出的图)。
在分析时,187 名患者有 28 天的结局。CRP(AUC:0.69,95%CI:0.59 至 0.78)、淋巴细胞计数(AUC:0.62,95%CI:0.53 至 0.72)和其他常规标志物均未预测主要结局。IL-6(AUC:0.77,0.65 至 0.88)和 suPAR(AUC:0.81,0.72 至 0.88)显示出一定的前景,但简单的临床特征,如 NEWS2 评分(AUC:0.70,0.60 至 0.79)或年龄(AUC:0.70,0.62 至 0.77)表现几乎一样好。
入院血液生物标志物对预测 COVID-19 结局仅有中等预测价值,而年龄和 NEWS2 评分等简单的临床特征优于许多生物标志物。IL-6 和 suPAR 的表现最好,进一步的研究应集中于这些生物标志物对常规护理的附加价值。