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中国武汉 COVID-19 患者炎症参数的纵向变化及其与疾病严重程度和结局的相关性。

Longitudinal changes of inflammatory parameters and their correlation with disease severity and outcomes in patients with COVID-19 from Wuhan, China.

机构信息

Department and Institute of Infectious Disease, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1095, Jiefang Avenue, Wuhan, 430030, China.

出版信息

Crit Care. 2020 Aug 27;24(1):525. doi: 10.1186/s13054-020-03255-0.

DOI:10.1186/s13054-020-03255-0
PMID:32854750
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7450961/
Abstract

BACKGROUND

Coronavirus disease 2019 (COVID-19) is a newly emerging infectious disease and rapidly escalating epidemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The pathogenesis of COVID-19 remains to be elucidated. We aimed to clarify correlation of systemic inflammation with disease severity and outcomes in COVID-19 patients.

METHODS

In this retrospective study, baseline characteristics, laboratory findings, and treatments were compared among 317 laboratory-confirmed COVID-19 patients with moderate, severe, or critically ill form of the disease. Moreover, the longitudinal changes of serum cytokines, lactate dehydrogenase (LDH), high-sensitivity C-reactive protein (hsCRP), and hsCRP to lymphocyte count ratio (hsCRP/L) as well as their associations with disease severity and outcomes were investigated in 68 COVID-19 patients.

RESULTS

Within 24 h of admission, the critically ill patients showed higher concentrations of inflammatory markers including serum soluble interleukin (IL)-2 receptor, IL-6, IL-8, IL-10, tumor necrosis factor alpha (TNF-α), ferritin, procalcitonin, LDH, hsCRP, and hsCRP/L than patients with severe or moderate disease. The severe cases displayed the similar response patterns when compared with moderate cases. The longitudinal assays showed the levels of pro-inflammatory cytokines, LDH, hsCRP, and hsCRP/L gradually declined within 10 days post admission in moderate, severe cases or those who survived. However, there was no significant reduction in cytokines, LDH, hsCRP, and hsCRP/L levels in critically ill or deceased patients throughout the course of illness. Compared with female patients, male cases showed higher serum concentrations of soluble IL-2R, IL-6, ferritin, procalcitonin, LDH, and hsCRP. Multivariate logistic regression analysis revealed that IL-6 > 50 pg/mL and LDH > 400 U/L on admission were independently associated with disease severity in patients with COVID-19.

CONCLUSION

Exuberant inflammatory responses within 24 h of admission in patients with COVID-19 may correlate with disease severity. SARS-CoV-2 infection appears to elicit a sex-based differential immune response. IL-6 and LDH were independent predictive parameters for assessing the severity of COVID-19. An early decline of these inflammation markers may be associated with better outcomes.

摘要

背景

新型冠状病毒病(COVID-19)是一种新出现的传染病和快速升级的流行病,由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起。COVID-19 的发病机制仍有待阐明。我们旨在阐明 COVID-19 患者全身炎症与疾病严重程度和结局的相关性。

方法

在这项回顾性研究中,我们比较了 317 例经实验室确诊的 COVID-19 患者中病情中度、重度或危重症患者的基线特征、实验室检查结果和治疗方法。此外,我们还在 68 例 COVID-19 患者中研究了血清细胞因子、乳酸脱氢酶(LDH)、高敏 C 反应蛋白(hsCRP)和 hsCRP 与淋巴细胞计数比值(hsCRP/L)的纵向变化及其与疾病严重程度和结局的关系。

结果

在入院后 24 小时内,危重症患者的血清可溶性白细胞介素(IL)-2 受体、IL-6、IL-8、IL-10、肿瘤坏死因子-α(TNF-α)、铁蛋白、降钙素原、LDH、hsCRP 和 hsCRP/L 等炎症标志物的浓度均高于重症或中度疾病患者。与中度疾病患者相比,重度患者也表现出类似的反应模式。纵向检测显示,在中度、重度或存活患者入院后 10 天内,促炎细胞因子、LDH、hsCRP 和 hsCRP/L 水平逐渐下降。然而,在整个病程中,危重症或死亡患者的细胞因子、LDH、hsCRP 和 hsCRP/L 水平没有明显降低。与女性患者相比,男性患者的血清可溶性 IL-2R、IL-6、铁蛋白、降钙素原、LDH 和 hsCRP 浓度更高。多变量逻辑回归分析显示,入院时 IL-6>50pg/ml 和 LDH>400U/L 与 COVID-19 患者的疾病严重程度独立相关。

结论

COVID-19 患者入院后 24 小时内过度的炎症反应可能与疾病严重程度相关。SARS-CoV-2 感染似乎引起了基于性别的不同免疫反应。IL-6 和 LDH 是评估 COVID-19 严重程度的独立预测参数。这些炎症标志物的早期下降可能与更好的结局相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56ce/7457239/709286858930/13054_2020_3255_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56ce/7457239/5de68d91f3a4/13054_2020_3255_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56ce/7457239/709286858930/13054_2020_3255_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56ce/7457239/5de68d91f3a4/13054_2020_3255_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56ce/7457239/709286858930/13054_2020_3255_Fig2_HTML.jpg

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