Department of Pulmonary Diseases and Clinical Allergology, Turku University Hospital and University of Turku, Turku, Finland.
Department of Infectious Diseases, Turku University Hospital and University of Turku, Turku, Finland.
BMC Infect Dis. 2022 Sep 28;22(1):755. doi: 10.1186/s12879-022-07753-0.
In this retrospective cohort study, we explored the correlation of blood human myxovirus resistance protein A (MxA) level with severity of disease in hospitalized COVID-19 patients.
All 304 patients admitted for COVID-19 in our hospital until 30th of April 2021 were included in this study. MxA was measured from peripheral blood samples in 268 cases. Patients were divided into groups based on their level of MxA on admission. We studied baseline characteristics and severity of disease on admission based on clinical parameters and inflammatory biomarker levels in each group. Severity of disease during hospitalization was determined by the applied level of respiratory support, by the usage of corticosteroids and by the duration of hospitalization.
Higher MxA levels on admission were associated with a shorter duration of symptoms before admission, and with more severe disease. Adjusted Odds Ratios for any respiratory support were 9.92 (95%CI 2.11-46.58; p = 0.004) in patients with MxA between 400 μg/L and 799 μg/L (p = 0.004) and 20.08 (95%CI 4.51-89.44; p < 0.001) in patients with MxA ≥ 800 μg/L in comparison with patients with initial MxA < 400 μg/L. The usage of corticosteroids was significantly higher in the high-MxA group (77%) in comparison with the intermediate-MxA group (62%, p = 0.013) and low-MxA group (47%, p < 0.001).
Higher initial levels of MxA were associated with more severe COVID-19. MxA may be a helpful additional biomarker to predict the severity of the disease.
在这项回顾性队列研究中,我们探讨了住院 COVID-19 患者血液中人粘病毒耐药蛋白 A(MxA)水平与疾病严重程度的相关性。
纳入 2021 年 4 月 30 日前我院收治的所有 304 例 COVID-19 患者,其中 268 例检测了外周血 MxA。根据入院时 MxA 水平将患者分为不同组。我们根据各组的临床参数和炎症生物标志物水平,研究入院时的基线特征和疾病严重程度。住院期间的疾病严重程度由所应用的呼吸支持水平、皮质类固醇的使用和住院时间来确定。
入院时较高的 MxA 水平与入院前症状持续时间较短和疾病更严重相关。对于任何呼吸支持,MxA 水平在 400μg/L 至 799μg/L 之间的患者(MxA 水平在 400μg/L 至 799μg/L 之间的患者)和 MxA 水平≥800μg/L 的患者(MxA 水平在 400μg/L 至 799μg/L 之间的患者)的调整比值比分别为 9.92(95%CI 2.11-46.58;p=0.004)和 20.08(95%CI 4.51-89.44;p<0.001),与初始 MxA<400μg/L 的患者相比。高 MxA 组(77%)比中 MxA 组(62%,p=0.013)和低 MxA 组(47%,p<0.001)使用皮质类固醇的比例明显更高。
较高的初始 MxA 水平与更严重的 COVID-19 相关。MxA 可能是一种有用的辅助生物标志物,有助于预测疾病的严重程度。