Department of Respiration, Affiliated Hospital of Jiaxing University/The First Hospital of Jiaxing, Jiaxing 314000, China.
Center for Pain Medicine, Affiliated Hospital of Jiaxing University/The First Hospital of Jiaxing, Jiaxing 314000, China.
Comput Math Methods Med. 2021 Jun 8;2021:9926249. doi: 10.1155/2021/9926249. eCollection 2021.
This study is aimed at exploring the relationship of the viral load of coronavirus disease 2019 (COVID-19) with lymphocyte count, neutrophil count, and C-reactive protein (CRP) and investigating the dynamic change of patients' viral load during the conversion from mild COVID-19 to severe COVID-19, so as to clarify the correlation between the viral load and progression of COVID-19.
This paper included 38 COVID-19 patients admitted to the First Hospital of Jiaxing from January 28, 2020, to March 6, 2020, and they were clinically classified according to the Guidelines on the Novel Coronavirus-Infected Pneumonia Diagnosis and Treatment. According to the instructions of the Nucleic Acid Detection Kit for the 2019 novel coronavirus (SARS-CoV-2), respiratory tract specimens (throat swabs) were collected from patients for nucleic acid testing. Patients' lymphocyte count and neutrophil count were determined by blood routine examination, and CRP was measured by biochemical test.
The results of our study suggested that the cycle threshold (Ct) value of Nucleocapsid protein (N) gene examined by nucleic acid test was markedly positively correlated with lymphocyte count ( = 0.0445, = 0.1203), but negatively correlated with neutrophil count ( = 0.0446, = 0.1167) and CRP ( = 0.0393, = 0.1261), which indicated that patients with a higher viral load tended to have lower lymphocyte count but higher neutrophil count and CRP. Additionally, we detected the dynamic change of Ct value in patients who developed into a severe case, finding that viral load of 3 patients increased before disease progression, whereas this phenomenon was not found in 2 patients with underlying diseases.
The results of this study demonstrated that viral load of SARS-CoV-2 is significantly negatively correlated with lymphocyte count, but markedly positively correlated with neutrophil count and CRP. The rise of viral load is very likely to be the key factor leading to the overloading of the body's immune response and resulting in the disease progression into severe disease.
本研究旨在探讨 2019 年冠状病毒病(COVID-19)的病毒载量与淋巴细胞计数、中性粒细胞计数和 C 反应蛋白(CRP)的关系,并探讨轻症 COVID-19 向重症 COVID-19 转化过程中患者病毒载量的动态变化,以阐明病毒载量与 COVID-19 进展的相关性。
本研究纳入了 2020 年 1 月 28 日至 3 月 6 日期间入住嘉兴市第一医院的 38 例 COVID-19 患者,根据《新型冠状病毒感染的肺炎诊疗方案》进行临床分类。根据新型冠状病毒(SARS-CoV-2)核酸检测试剂盒说明书,采集患者呼吸道标本(咽拭子)进行核酸检测。通过血常规检查测定患者的淋巴细胞计数和中性粒细胞计数,通过生化试验测定 CRP。
本研究结果表明,核酸检测中核衣壳蛋白(N)基因的循环阈值(Ct)值与淋巴细胞计数呈显著正相关( = 0.0445, = 0.1203),与中性粒细胞计数呈负相关( = 0.0446, = 0.1167),与 CRP 呈负相关( = 0.0393, = 0.1261),提示病毒载量较高的患者淋巴细胞计数较低,但中性粒细胞计数和 CRP 较高。此外,我们检测了发展为重症病例患者的 Ct 值的动态变化,发现 3 例患者在疾病进展前病毒载量增加,而 2 例有基础疾病的患者则没有发现这种现象。
本研究结果表明,SARS-CoV-2 的病毒载量与淋巴细胞计数呈显著负相关,与中性粒细胞计数和 CRP 呈显著正相关。病毒载量的升高很可能是导致机体免疫反应超负荷并导致疾病进展为重症的关键因素。