Ji Pan, Zhu Jieyun, Zhong Zhimei, Li Hongyuan, Pang Jielong, Li Bocheng, Zhang Jianfeng
Department of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University, Nanning, China.
Medicine (Baltimore). 2020 Nov 20;99(47):e23315. doi: 10.1097/MD.0000000000023315.
Our study aimed to assess the existing evidence on whether severe coronavirus disease 2019 (COVID-19) is associated with elevated inflammatory markers.The PubMed, Embase, Web of Science, Scopus, Chinese National Knowledge Infrastructure, WanFang, and China Science and Technology Journal databases were searched to identify studies published between January 1 and April 21, 2020 that assayed inflammatory markers in COVID-19 patients. Three reviewers independently examined the literature, extracted relevant data, and assessed the risk of publication bias before including the meta-analysis studies.Fifty-six studies involving 8719 COVID-19 patients were identified. Meta-analysis showed that patients with severe disease showed elevated levels of white blood cell count (WMD: 1.15, 95% CI: 0.78-1.52), C-reactive protein (WMD: 38.85, 95% CI: 31.19-46.52), procalcitonin (WMD: 0.08, 95% CI: 0.06-0.11), erythrocyte sedimentation rate (WMD: 10.15, 95% CI: 5.03-15.46), interleukin-6 (WMD: 23.87, 95% CI: 15.95-31.78), and interleukin-10 (WMD: 2.12, 95% CI: 1.97-2.28). Similarly, COVID-19 patients who died during follow-up showed significantly higher levels of white blood cell count (WMD: 4.11, 95% CI: 3.25-4.97), C-reactive protein (WMD: 74.18, 95% CI: 56.63-91.73), procalcitonin (WMD: 0.26, 95% CI: 0.11-0.42), erythrocyte sedimentation rate (WMD: 10.94, 95% CI: 4.79-17.09), and interleukin-6 (WMD: 59.88, 95% CI: 19.46-100.30) than survivors.Severe COVID-19 is associated with higher levels of inflammatory markers than a mild disease, so tracking these markers may allow early identification or even prediction of disease progression.
我们的研究旨在评估关于重症2019冠状病毒病(COVID-19)是否与炎症标志物升高相关的现有证据。检索了PubMed、Embase、Web of Science、Scopus、中国知网、万方和中国科技期刊数据库,以识别2020年1月1日至4月21日期间发表的检测COVID-19患者炎症标志物的研究。三位评审员独立审查文献、提取相关数据并评估发表偏倚风险,然后纳入荟萃分析研究。共识别出56项涉及8719例COVID-19患者的研究。荟萃分析表明,重症患者的白细胞计数(加权均数差:1.15,95%置信区间:0.78 - 1.52)、C反应蛋白(加权均数差:38.85,95%置信区间:31.19 - 46.52)、降钙素原(加权均数差:0.08,95%置信区间:0.06 - 0.11)、红细胞沉降率(加权均数差:10.15,95%置信区间:5.03 - 15.46)、白细胞介素-6(加权均数差:23.87,95%置信区间:15.95 - 31.78)和白细胞介素-10(加权均数差:2.12,95%置信区间:1.97 - 2.28)水平升高。同样,随访期间死亡的COVID-19患者的白细胞计数(加权均数差:4.11,95%置信区间:3.25 - 4.97)、C反应蛋白(加权均数差:74.18,95%置信区间:56.63 - 91.73)、降钙素原(加权均数差:0.26,95%置信区间:0.11 - 0.42)、红细胞沉降率(加权均数差:10.94,95%置信区间:4.79 - 17.09)和白细胞介素-6(加权均数差:59.88,95%置信区间:19.46 - 100.30)水平显著高于存活患者。与轻症疾病相比,重症COVID-19与更高水平的炎症标志物相关,因此追踪这些标志物可能有助于早期识别甚至预测疾病进展。