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用于预测 COVID-19 进展的新型生物标志物:一项回顾性、多中心队列研究。

Novel biomarkers for the prediction of COVID-19 progression a retrospective, multi-center cohort study.

机构信息

Department of Hematology, Zhongnan Hospital of Wuhan University , Wuhan, China.

Department of Urology, Zhongnan Hospital of Wuhan University , Wuhan, China.

出版信息

Virulence. 2020 Dec;11(1):1569-1581. doi: 10.1080/21505594.2020.1840108.

DOI:10.1080/21505594.2020.1840108
PMID:33172355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7671095/
Abstract

A pandemic designated as Coronavirus Disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is spreading worldwide. Up to date, there is no efficient biomarker for the timely prediction of the disease progression in patients. To analyze the inflammatory profiles of COVID-19 patients and demonstrate their implications for the illness progression of COVID-19. Retrospective analysis of 3,265 confirmed COVID-19 cases hospitalized between 10 January 2020, and 26 March 2020 in three medical centers in Wuhan, China. Patients were diagnosed as COVID-19 and hospitalized in Leishenshan Hospital, Zhongnan Hospital of Wuhan University and The Seventh Hospital of Wuhan, China. Univariable and multivariable logistic regression models were used to determine the possible risk factors for disease progression. Moreover, cutoff values, the sensitivity and specificity of inflammatory parameters for disease progression were determined by MedCalc Version 19.2.0. Age (95%CI, 1.017 to 1.048; < 0.001), serum amyloid A protein (SAA) (95%CI, 1.216 to 1.396; < 0.001) and erythrocyte sedimentation rate (ESR) (95%CI, 1.006 to 1.045; < 0.001) were likely the risk factors for the disease progression. The Area under the curve (AUC) of SAA for the progression of COVID-19 was 0.923, with the best predictive cutoff value of SAA of 12.4 mg/L, with a sensitivity of 83.9% and a specificity of 97.67%. SAA-containing parameters are novel promising ones for predicting disease progression in COVID-19.

摘要

一种由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的被指定为 2019 年冠状病毒病(COVID-19)的大流行病正在全球范围内传播。迄今为止,尚无用于及时预测患者疾病进展的有效生物标志物。为了分析 COVID-19 患者的炎症特征,并证明其对 COVID-19 疾病进展的影响。对 2020 年 1 月 10 日至 3 月 26 日期间在中国武汉的三个医疗中心住院的 3265 例确诊 COVID-19 病例进行回顾性分析。患者被诊断为 COVID-19 并在雷神山医院、武汉大学中南医院和武汉市第七医院住院。采用单变量和多变量逻辑回归模型确定疾病进展的可能危险因素。此外,通过 MedCalc Version 19.2.0 确定炎症参数对疾病进展的截断值、敏感性和特异性。年龄(95%CI,1.017 至 1.048;<0.001)、血清淀粉样蛋白 A 蛋白(SAA)(95%CI,1.216 至 1.396;<0.001)和红细胞沉降率(ESR)(95%CI,1.006 至 1.045;<0.001)可能是疾病进展的危险因素。SAA 用于 COVID-19 进展的曲线下面积(AUC)为 0.923,SAA 的最佳预测截断值为 12.4mg/L,灵敏度为 83.9%,特异性为 97.67%。含 SAA 的参数是预测 COVID-19 疾病进展的有前途的新参数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ad2/7671095/ab00629ed7b0/KVIR_A_1840108_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ad2/7671095/4a0ced27832d/KVIR_A_1840108_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ad2/7671095/3ea153f28e6c/KVIR_A_1840108_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ad2/7671095/ab00629ed7b0/KVIR_A_1840108_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ad2/7671095/4a0ced27832d/KVIR_A_1840108_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ad2/7671095/3ea153f28e6c/KVIR_A_1840108_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ad2/7671095/ab00629ed7b0/KVIR_A_1840108_F0003_OC.jpg

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