Nepean Clinical School, University of Sydney, Sydney, New South Wales, Australia
Centre for Immunology and Allergy Research, Westmead Institute for Medical Research, Westmead, New South Wales, Australia.
BMJ Open. 2021 Jan 6;11(1):e044497. doi: 10.1136/bmjopen-2020-044497.
Accurate triage is an important first step to effectively manage the clinical treatment of severe cases in a pandemic outbreak. In the current COVID-19 global pandemic, there is a lack of reliable clinical tools to assist clinicians to perform accurate triage. Host response biomarkers have recently shown promise in risk stratification of disease progression; however, the role of these biomarkers in predicting disease progression in patients with COVID-19 is unknown. Here, we present a protocol outlining a prospective validation study to evaluate the biomarkers' performance in predicting clinical outcomes of patients with COVID-19.
This prospective validation study assesses patients infected with COVID-19, in whom blood samples are prospectively collected. Recruited patients include a range of infection severity from asymptomatic to critically ill patients, recruited from the community, outpatient clinics, emergency departments and hospitals. Study samples consist of peripheral blood samples collected into RNA-preserving (PAXgene/Tempus) tubes on patient presentation or immediately on study enrolment. Real-time PCR (RT-PCR) will be performed on total RNA extracted from collected blood samples using primers specific to host response gene expression biomarkers that have been previously identified in studies of respiratory viral infections. The RT-PCR data will be analysed to assess the diagnostic performance of individual biomarkers in predicting COVID-19-related outcomes, such as viral pneumonia, acute respiratory distress syndrome or bacterial pneumonia. Biomarker performance will be evaluated using sensitivity, specificity, positive and negative predictive values, likelihood ratios and area under the receiver operating characteristic curve.
This research protocol aims to study the host response gene expression biomarkers in severe respiratory viral infections with a pandemic potential (COVID-19). It has been approved by the local ethics committee with approval number 2020/ETH00886. The results of this project will be disseminated in international peer-reviewed scientific journals.
准确分诊是有效管理大流行疫情期间重症病例临床治疗的重要第一步。在当前的 COVID-19 全球大流行中,缺乏可靠的临床工具来协助临床医生进行准确分诊。宿主反应生物标志物最近在疾病进展风险分层方面显示出了希望;然而,这些生物标志物在预测 COVID-19 患者疾病进展中的作用尚不清楚。在这里,我们提出了一个方案,概述了一项前瞻性验证研究,以评估生物标志物在预测 COVID-19 患者临床结局中的表现。
这项前瞻性验证研究评估了感染 COVID-19 的患者,前瞻性地采集了他们的血液样本。招募的患者包括从无症状到重症患者的一系列感染严重程度,从社区、门诊诊所、急诊室和医院招募。研究样本包括患者就诊时或入组时立即采集到的保存 RNA 的(PAXgene/Tempus)管中的外周血样本。使用先前在呼吸道病毒感染研究中鉴定的针对宿主反应基因表达生物标志物的引物,从收集的血液样本中提取总 RNA,然后进行实时 PCR(RT-PCR)。将分析 RT-PCR 数据,以评估单个生物标志物在预测 COVID-19 相关结局(如病毒性肺炎、急性呼吸窘迫综合征或细菌性肺炎)方面的诊断性能。将使用灵敏度、特异性、阳性和阴性预测值、似然比和受试者工作特征曲线下面积来评估生物标志物的性能。
本研究方案旨在研究具有大流行潜力的严重呼吸道病毒感染(COVID-19)中的宿主反应基因表达生物标志物。该方案已获得当地伦理委员会的批准,批准编号为 2020/ETH00886。本项目的结果将在国际同行评议的科学期刊上发表。