Ramalho-Pinto Cecília Horta, Ventura Lucas Haniel Araújo, Camatta Giovanna Caliman, Silveira-Nunes Gabriela, Gomes Matheus Souza, Sato Hugo Itaru, Costa Murilo Soares, Guimarães Henrique Cerqueira, Barbuto Rafael Calvão, Martins-Filho Olindo Assis, Amaral Laurence Rodrigues, Bertarini Pedro Luiz Lima, Teixeira Santuza Maria Ribeiro, Tupinambás Unaí, Teixeira-Carvalho Andrea, Faria Ana Maria Caetano
Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Pres. Antônio Carlos, 6627, 31270-901, Belo Horizonte, Brazil.
Departamento de Medicina, Universidade Federal de Juiz de Fora, Av. Doutor Raimundo Monteiro Resende, 330, 35010-177, Governador Valadares, Brazil.
J Leukoc Biol. 2025 Feb 13;117(2). doi: 10.1093/jleuko/qiae223.
Although the SARS-CoV-2 infection has established risk groups, identifying biomarkers for disease outcomes is still crucial to stratify patient risk and enhance clinical management. Optimal efficacy of COVID-19 antiviral medications relies on early administration within the initial 5 d of symptoms, assisting high-risk patients in avoiding hospitalization and improving survival chances. The complete blood count (CBC) can be an efficient and affordable option to find biomarkers that predict the COVID-19 prognosis due to infection-induced alterations in various blood parameters. This study aimed to associate hematological parameters with different COVID-19 clinical forms and utilizes them as disease outcome predictors. We performed a CBC in blood samples from 297 individuals with COVID-19 from Belo Horizonte, Brazil. Statistical analysis, as well as ROC Curves and machine learning Decision Tree algorithms were used to identify correlations, and their accuracy, between blood parameters and disease severity. In the initial 4 d of infection, traditional hematological COVID-19 alterations, such as lymphopenia, were not yet apparent. However, the monocyte percentage and granulocyte-to-lymphocyte ratio (GLR) proved to be reliable predictors for hospitalization, even in cases where patients exhibited mild symptoms that later progressed to hospitalization. Thus, our findings demonstrate that COVID-19 patients with monocyte percentages lower than 7.7% and a GLR higher than 8.75 are assigned to the hospitalized group with a precision of 86%. This suggests that these variables can serve as important biomarkers in predicting disease outcomes and could be used to differentiate patients at hospital admission for managing therapeutic interventions, including early antiviral administration. Moreover, they are simple parameters that can be useful in minimally equipped health care units.
尽管严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染已确定了风险群体,但确定疾病预后的生物标志物对于分层患者风险和加强临床管理仍然至关重要。新型冠状病毒肺炎(COVID-19)抗病毒药物的最佳疗效依赖于在症状出现后的最初5天内尽早给药,以帮助高危患者避免住院并提高生存几率。全血细胞计数(CBC)可能是一种有效且经济实惠的方法,用于寻找因感染导致各种血液参数改变而预测COVID-19预后的生物标志物。本研究旨在将血液学参数与不同的COVID-19临床类型相关联,并将其用作疾病预后的预测指标。我们对来自巴西贝洛奥里藏特的297例COVID-19患者的血液样本进行了全血细胞计数。使用统计分析以及ROC曲线和机器学习决策树算法来确定血液参数与疾病严重程度之间的相关性及其准确性。在感染的最初4天,传统的COVID-19血液学改变,如淋巴细胞减少症,尚不明显。然而,单核细胞百分比和粒细胞与淋巴细胞比值(GLR)被证明是住院的可靠预测指标,即使在患者表现出轻微症状但后来进展为住院的情况下也是如此。因此,我们的研究结果表明,单核细胞百分比低于7.7%且GLR高于8.75的COVID-19患者被归入住院组,准确率为86%。这表明这些变量可作为预测疾病预后的重要生物标志物,并可用于在入院时区分患者,以管理治疗干预措施,包括早期抗病毒给药。此外,它们是简单的参数,在设备简陋的医疗保健单位可能会有用。