National Institute for Infectious Diseases, Lazzaro Spallanzani, IRCCS, Rome, Italy.
Centre de Recherche en Infectiologie de l'Université Laval, Quebec City, QC, Canada.
PLoS One. 2020 Dec 28;15(12):e0244129. doi: 10.1371/journal.pone.0244129. eCollection 2020.
Detailed temporal analyses of complete (full) blood count (CBC) parameters, their evolution and relationship to patient age, gender, co-morbidities and management outcomes in survivors and non-survivors with COVID-19 disease, could identify prognostic clinical biomarkers.
From 29 January 2020 until 28 March 2020, we performed a longitudinal cohort study of COVID-19 inpatients at the Italian National Institute for Infectious Diseases, Rome, Italy. 9 CBC parameters were studied as continuous variables [neutrophils, lymphocytes, monocytes, platelets, mean platelet volume, red blood cell count, haemoglobin concentration, mean red blood cell volume and red blood cell distribution width (RDW %)]. Model-based punctual estimates, as average of all patients' values, and differences between survivors and non-survivors, overall, and by co-morbidities, at specific times after symptoms, with relative 95% CI and P-values, were obtained by marginal prediction and ANOVA- style joint tests. All analyses were carried out by STATA 15 statistical package.
379 COVID-19 patients [273 (72% were male; mean age was 61.67 (SD 15.60)] were enrolled and 1,805 measures per parameter were analysed. Neutrophils' counts were on average significantly higher in non-survivors than in survivors (P<0.001) and lymphocytes were on average higher in survivors (P<0.001). These differences were time dependent. Average platelets' counts (P<0.001) and median platelets' volume (P<0.001) were significantly different in survivors and non-survivors. The differences were time dependent and consistent with acute inflammation followed either by recovery or by death. Anaemia with anisocytosis was observed in the later phase of COVID-19 disease in non-survivors only. Mortality was significantly higher in patients with diabetes (OR = 3.28; 95%CI 1.51-7.13; p = 0.005), obesity (OR = 3.89; 95%CI 1.51-10.04; p = 0.010), chronic renal failure (OR = 9.23; 95%CI 3.49-24.36; p = 0.001), COPD (OR = 2.47; 95% IC 1.13-5.43; p = 0.033), cardiovascular diseases (OR = 4.46; 95%CI 2.25-8.86; p = 0.001), and those >60 years (OR = 4.21; 95%CI 1.82-9.77; p = 0.001). Age (OR = 2.59; 95%CI 1.04-6.45; p = 0.042), obesity (OR = 5.13; 95%CI 1.81-14.50; p = 0.002), renal chronic failure (OR = 5.20; 95%CI 1.80-14.97; p = 0.002) and cardiovascular diseases (OR 2.79; 95%CI 1.29-6.03; p = 0.009) were independently associated with poor clinical outcome at 30 days after symptoms' onset.
Increased neutrophil counts, reduced lymphocyte counts, increased median platelet volume and anaemia with anisocytosis, are poor prognostic indicators for COVID19, after adjusting for the confounding effect of obesity, chronic renal failure, COPD, cardiovascular diseases and age >60 years.
对完整(全)血细胞计数(CBC)参数进行详细的时间分析,及其在 COVID-19 幸存者和非幸存者中的演变以及与患者年龄、性别、合并症和管理结果的关系,可能会识别出预后的临床生物标志物。
从 2020 年 1 月 29 日至 2020 年 3 月 28 日,我们在意大利罗马的意大利国家传染病研究所对 COVID-19 住院患者进行了一项纵向队列研究。我们将 9 个 CBC 参数作为连续变量进行研究[中性粒细胞、淋巴细胞、单核细胞、血小板、血小板平均体积、红细胞计数、血红蛋白浓度、平均红细胞体积和红细胞分布宽度(RDW%)]。通过边际预测和 ANOVA 风格联合检验,获得了模型基的点估计值(作为所有患者值的平均值)以及幸存者和非幸存者之间的差异,以及在症状出现后的特定时间点,以及相对 95%置信区间(CI)和 P 值。所有分析均使用 STATA 15 统计软件包进行。
共纳入 379 名 COVID-19 患者[273 名(72%为男性;平均年龄为 61.67(SD 15.60)],分析了 1805 次参数测量。非幸存者的中性粒细胞计数平均显著高于幸存者(P<0.001),幸存者的淋巴细胞计数平均较高(P<0.001)。这些差异是时间依赖的。血小板平均计数(P<0.001)和血小板平均体积中位数(P<0.001)在幸存者和非幸存者之间有显著差异。这些差异是时间依赖的,与急性炎症后恢复或死亡一致。仅在非幸存者的 COVID-19 疾病后期观察到贫血伴红细胞大小不均。在调整肥胖、慢性肾功能衰竭、COPD、心血管疾病和年龄>60 岁的混杂因素后,糖尿病(OR=3.28;95%CI 1.51-7.13;p=0.005)、肥胖(OR=3.89;95%CI 1.51-10.04;p=0.010)、慢性肾功能衰竭(OR=9.23;95%CI 3.49-24.36;p=0.001)、COPD(OR=2.47;95%CI 1.13-5.43;p=0.033)和心血管疾病(OR=4.46;95%CI 2.25-8.86;p=0.001)患者的死亡率显著更高,年龄>60 岁(OR=4.21;95%CI 1.82-9.77;p=0.001)。年龄(OR=2.59;95%CI 1.04-6.45;p=0.042)、肥胖(OR=5.13;95%CI 1.81-14.50;p=0.002)、慢性肾功能衰竭(OR=5.20;95%CI 1.80-14.97;p=0.002)和心血管疾病(OR 2.79;95%CI 1.29-6.03;p=0.009)在症状出现后 30 天与不良临床结局独立相关。
在调整肥胖、慢性肾功能衰竭、COPD、心血管疾病和年龄>60 岁的混杂因素后,中性粒细胞计数增加、淋巴细胞计数减少、血小板平均体积增加和贫血伴红细胞大小不均,是 COVID19 的预后不良指标。