Laboratory of Hematology, Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Paris, France; Université de Paris, Institut Cochin, CNRS UMR8104, INSERM U1016, Paris, France.
Department of Biostatistics and Epidemiology, Gustave Roussy Cancer Center, Villejuif, France; Université Paris-Saclay, INSERM U1018, Gustave Roussy Cancer Center, Villejuif, France.
EBioMedicine. 2022 Jun;80:104077. doi: 10.1016/j.ebiom.2022.104077. Epub 2022 May 26.
Severe COVID-19 is associated with a high circulating level of calprotectin, the S100A8/S100A9 alarmin heterodimer. Baseline calprotectin amount measured in peripheral blood at diagnosis correlates with disease severity. The optimal use of this biomarker along COVID-19 course remains to be delineated.
We focused on patients with a WHO-defined moderate COVID-19 requiring hospitalization in a medical ward. We collected plasma and serum from three independent cohorts (N = 626 patients) and measured calprotectin amount at admission. We performed longitudinal measures of calprotectin in 457 of these patients (1461 samples) and used a joint latent class mixture model in which classes were defined by age, body mass index and comorbidities to identify calprotectin trajectories predicting the risk of transfer into an intensive care unit or death.
After adjustment for age, sex, body mass index and comorbidities, the predictive value of baseline calprotectin in patients with moderate COVID19 could be refined by serial monitoring of the biomarker. We discriminated three calprotectin trajectories associated with low, moderate, and high risk of poor outcome, and we designed an algorithm available as online software (https://calpla.gustaveroussy.fr:8443/) to monitor the probability of a poor outcome in individual patients with moderate COVID-19.
These results emphasize the clinical interest of serial monitoring of calprotectin amount in the peripheral blood to anticipate the risk of poor outcomes in patients with moderate COVID-19 hospitalized in a standard care unit.
The study received support (research grants) from ThermoFisher immunodiagnostics (France) and Gustave Roussy Foundation.
严重的 COVID-19 与循环中高浓度的钙卫蛋白(S100A8/S100A9 警报素异二聚体)有关。诊断时外周血中钙卫蛋白的基线量与疾病严重程度相关。该生物标志物在 COVID-19 病程中的最佳应用仍有待阐明。
我们专注于因世界卫生组织定义的中度 COVID-19 而需要住院治疗的患者。我们从三个独立的队列(N=626 例患者)中收集了血浆和血清,并在入院时测量了钙卫蛋白的含量。我们对其中 457 例患者(1461 个样本)进行了钙卫蛋白的纵向测量,并使用联合潜在类别混合模型,其中类别由年龄、体重指数和合并症定义,以确定预测转入重症监护病房或死亡风险的钙卫蛋白轨迹。
在校正年龄、性别、体重指数和合并症后,中度 COVID19 患者基线钙卫蛋白的预测价值可以通过对生物标志物的连续监测来优化。我们区分了三种钙卫蛋白轨迹,与低、中、高不良结局风险相关,并且我们设计了一种可作为在线软件(https://calpla.gustaveroussy.fr:8443/)使用的算法,以监测个体中度 COVID-19 患者不良结局的可能性。
这些结果强调了连续监测外周血中钙卫蛋白量以预测在标准护理病房住院的中度 COVID-19 患者不良结局风险的临床意义。
该研究得到了 ThermoFisher 免疫诊断学(法国)和 Gustave Roussy 基金会的支持(研究资助)。