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唾液中 SARS-CoV-2 感染的病毒载量动力学:一项前瞻性多中心比较研究。

Viral Load Kinetics of SARS-CoV-2 Infection in Saliva in Korean Patients: a Prospective Multi-center Comparative Study.

机构信息

Department of Infectious Diseases, Chonnam National University Hospital, Gwangju, Korea.

Department of Infectious Diseases, Keimyung University Dongsan Hospital, Daegu, Korea.

出版信息

J Korean Med Sci. 2020 Aug 10;35(31):e287. doi: 10.3346/jkms.2020.35.e287.

Abstract

BACKGROUND

This study was performed to compare the viral load and kinetics of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) in saliva with those in standard nasopharyngeal/oropharyngeal (NP/OP) swabs.

METHODS

Fifteen patients with SARS-CoV-2 infection from four hospitals were prospectively enrolled and matched samples of nasopharyngeal/oropharyngeal swabs and saliva were collected at Day 1 of admission and every other day till consequently negative for two times. Real-time reverse transcription polymerase chain reaction (rRT-PCR) was performed to detect the envelope (E) and RNA-dependent RNA polymerase (RdRP) genes.

RESULTS

The cycle threshold values of saliva were comparable to those of NP/OP swabs overall ( = 0.720, Mann-Whitney U test). However, the overall sensitivity of rRT-PCR using saliva was 64% (34/53), which is lower than the 77% (41/53) using NP/OP swabs. The sensitivity of rRT-PCR using saliva was especially lower in early stage of symptom onset (1-5 days; 8/15; 53%) and in patients who did not have sputum (12/22; 55%).

CONCLUSION

Saliva sample itself is not appropriate for initial diagnosis of coronavirus disease 2019 (COVID-19) to replace NP/OP swabs, especially for the person who does not produce sputum. COVID-19 cannot be excluded when the test using saliva is negative, and it is necessary to retest using NP/OP swabs.

摘要

背景

本研究旨在比较唾液与标准鼻咽/口咽(NP/OP)拭子中严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的病毒载量和动力学。

方法

从四家医院前瞻性招募了 15 名 SARS-CoV-2 感染患者,在入院第 1 天和随后连续两次阴性时,采集鼻咽/口咽拭子和唾液的匹配样本。采用实时逆转录聚合酶链反应(rRT-PCR)检测包膜(E)和 RNA 依赖性 RNA 聚合酶(RdRP)基因。

结果

总体而言,唾液的循环阈值与 NP/OP 拭子相当(=0.720,Mann-Whitney U 检验)。然而,使用唾液的 rRT-PCR 总体灵敏度为 64%(34/53),低于使用 NP/OP 拭子的 77%(41/53)。在症状发作的早期(1-5 天;15 例中的 8 例;53%)和没有痰液的患者(22 例中的 12 例;55%)中,使用唾液的 rRT-PCR 灵敏度尤其较低。

结论

唾液样本本身不适合替代 NP/OP 拭子作为 2019 年冠状病毒病(COVID-19)的初始诊断,尤其是对于不产生痰液的患者。当使用唾液进行的检测为阴性时,不能排除 COVID-19,有必要使用 NP/OP 拭子重新检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc8f/7415999/1f1fa1723a03/jkms-35-e287-g001.jpg

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