Laboratory and genetic predictors for severe COVID-19 infection

被引:0
作者
Kadiyska, Tanya [1 ,2 ]
Cherneva, Radostina [3 ]
Cherneva, Zheina [4 ]
Marchev, Sotir [4 ]
Madzharova, Dilyana [2 ]
Tourtourikov, Ivan [2 ,5 ]
Mitev, Vanyo [5 ]
机构
[1] Med Univ Sofia, Dept Physiol & Pathophysiol, Sofia, Bulgaria
[2] Genica & Genome Ctr Bulgaria, Genet Med Diagnost Lab, Sofia, Bulgaria
[3] Univ Hosp Resp Dis St Sophia, Sofia, Bulgaria
[4] Minist Internal Affairs, Med Inst, Clin Cardiol, Sofia, Bulgaria
[5] Med Univ Sofia, Dept Med Chem & Biochem, Sofia, Bulgaria
关键词
COVID-19; OAS1; laboratory and genetic predictors; CLINICAL CHARACTERISTICS; CYTOKINE; WUHAN;
D O I
10.3897/pharmacia.71.e120638
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study aims to identify laboratory and genetic markers important for COVID-19 severity to improve patient assessment and treatment. COVID-19 patients were divided into two groups based on disease severity. Clinical, laboratory (complete blood count, complete biochemical parameters - lactate dehydrogenase (LDH), serum ferritin), and genetic markers (OAST rs4767027) were analyzed. A total of 61 COVID-19 patients and 48 negative controls were investigated. Group I showed more often lymphopenia - 3.16 (1.39-3.89) vs 5.61(4.21-7.98), p-0.027 and thrombocytopenia - 165 (75-256) vs 212 (198-349), p-0.031, higher LDH (621 +/- 218 U/L vs 312 +/- 110 U/L), p-0.014. OAS1 rs4767027 genotype and allele frequencies did not differ significantly from worldwide population frequencies. Lymphopenia and thrombocytopenia are likely associated with immune inflammation and COVID-19 severity. While increased OAS1 transcript levels are correlated with reduced risk of infection, they can contribute to NLRP3 inflammasome activation once the infection has been established.
引用
收藏
页码:1 / 8
页数:8
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