Zinellu Angelo, Mangoni Arduino A
Department of Biomedical Sciences, University of Sassari, Sassari, Italy.
Discipline of Clinical Pharmacology, College of Medicine and Public Health, Flinders University, Adelaide, Australia.
Expert Rev Clin Immunol. 2022 Nov;18(11):1187-1202. doi: 10.1080/1744666X.2022.2120472. Epub 2022 Sep 5.
Severe manifestations of coronavirus disease 2019 (COVID-19) are associated with alterations in blood cells that regulate immunity, inflammation, and hemostasis. We conducted an updated systematic review and meta-analysis of the association between the neutrophil, lymphocyte, and platelet count, neutrophil-to-lymphocyte ratio (NLR), and platelet-to-lymphocyte ratio (PLR), and COVID-19 progression and mortality.
A systematic literature search was conducted in PubMed, Web of Science, and Scopus for studies published between January 2020 and June 2022.
In 71 studies reporting the investigated parameters within 48 hours of admission, higher NLR (HR 1.21, 95% CI 1.16 to 1.27, p < 0.0001), relative neutrophilia (HR 1.62, 95% CI 1.46 to 1.80, p < 0.0001), relative lymphopenia (HR 1.62, 95% CI 1.27 to 2.08, p < 0.001), and relative thrombocytopenia (HR 1.74, 95% CI 1.36 to 2.22, p < 0.001), but not PLR (p = 0.11), were significantly associated with disease progression and mortality. Between-study heterogeneity was large-to-extreme. The magnitude and direction of the effect size were not modified in sensitivity analysis.
NLR and neutrophil, lymphocyte, and platelet count significantly discriminate COVID-19 patients with different progression and survival outcomes. (PROSPERO registration number: CRD42021267875).
2019冠状病毒病(COVID-19)的严重表现与调节免疫、炎症和止血的血细胞变化有关。我们对中性粒细胞、淋巴细胞和血小板计数、中性粒细胞与淋巴细胞比值(NLR)以及血小板与淋巴细胞比值(PLR)与COVID-19进展和死亡率之间的关联进行了更新的系统评价和荟萃分析。
在PubMed、Web of Science和Scopus中对2020年1月至2022年6月发表的研究进行系统文献检索。
在71项报告入院后48小时内研究参数的研究中,较高的NLR(风险比1.21,95%置信区间1.16至1.27,p<0.0001)、相对中性粒细胞增多(风险比1.62,95%置信区间1.46至1.80,p<0.0001)、相对淋巴细胞减少(风险比1.62,95%置信区间1.27至2.08,p<0.001)和相对血小板减少(风险比1.74,95%置信区间1.36至2.22,p<0.001)与疾病进展和死亡率显著相关,但PLR无相关性(p=0.11)。研究间异质性大到极端。敏感性分析中效应量的大小和方向未改变。
NLR以及中性粒细胞、淋巴细胞和血小板计数可显著区分具有不同进展和生存结果的COVID-19患者。(国际前瞻性系统评价注册编号:CRD42021267875)