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
相关论文
共 46 条
  • [1] Better outcome of COVID-19 positive kidney transplant recipients during the unremitting stage with optimized anticoagulation and immunosuppression
    AlOtaibi, Torki M.
    Gheith, Osama A.
    Abuelmagd, Mohammed M.
    Adel, Mohammed
    Alqallaf, Ahmed K.
    Elserwy, Nabil A.
    Shaker, Mohamed
    Abbas, Ahmad M.
    Nagib, Ayman M.
    Nair, Prasad
    Halim, Medhat A.
    Mahmoud, Tarek
    Khaled, Mahmoud M.
    Hammad, Mohamed A.
    Fayyad, Zoheer A.
    Atta, Ahmed F.
    Mostafa, Ahmed Y.
    Draz, Ahmed S.
    Zakaria, Zakaria E.
    Atea, Khaled A.
    Aboatya, Hasaneen H.
    Ameenn, Mohamed E.
    Monem, Mohamed A.
    Mahmoud, Amro M.
    [J]. CLINICAL TRANSPLANTATION, 2021, 35 (06)
  • [2] Variation in antiviral 2′,5′-oligoadenylate synthetase (2′5′AS) enzyme activity is controlled by a single-nucleotide polymorphism at a splice-acceptor site in the OAS1 gene
    Bonnevie-Nielsen, V
    Field, LL
    Lu, S
    Zheng, DJ
    Li, M
    Martensen, PM
    Nielsen, TB
    Beck-Nielsen, H
    Lau, YL
    Pociot, F
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (04) : 623 - 633
  • [3] Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study
    Chen, Nanshan
    Zhou, Min
    Dong, Xuan
    Qu, Jieming
    Gong, Fengyun
    Han, Yang
    Qiu, Yang
    Wang, Jingli
    Liu, Ying
    Wei, Yuan
    Xia, Jia'an
    Yu, Ting
    Zhang, Xinxin
    Zhang, Li
    [J]. LANCET, 2020, 395 (10223) : 507 - 513
  • [4] Is COVID-19 a New Hematologic Disease?
    Debuc, Benjamin
    Smadja, David M.
    [J]. STEM CELL REVIEWS AND REPORTS, 2021, 17 (01) : 4 - 8
  • [5] Predictors of mortality for patients with COVID-19 pneumonia caused by SARS-CoV-2: a prospective cohort study
    Du, Rong-Hui
    Liang, Li-Rong
    Yang, Cheng-Qing
    Wang, Wen
    Cao, Tan-Ze
    Li, Ming
    Guo, Guang-Yun
    Du, Juan
    Zheng, Chun-Lan
    Zhu, Qi
    Hu, Ming
    Li, Xu-Yan
    Peng, Peng
    Shi, Huan-Zhong
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2020, 55 (05)
  • [6] COVID-19 and the clinical hematology laboratory
    Frater, John L.
    Zini, Gina
    D'Onofrio, Giuseppe
    Rogers, Heesun J.
    [J]. INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2020, 42 : 11 - 18
  • [7] Targeting the NLRP3 Inflammasome in Severe COVID-19
    Freeman, Tracey L.
    Swartz, Talia H.
    [J]. FRONTIERS IN IMMUNOLOGY, 2020, 11
  • [8] Clinical characteristics of coronavirus disease 2019 (COVID-19) in China: A systematic review and meta-analysis
    Fu, Leiwen
    Wang, Bingyi
    Yuan, Tanwei
    Chen, Xiaoting
    Ao, Yunlong
    Fitzpatrick, Thomas
    Li, Peiyang
    Zhou, Yiguo
    Lin, Yi-fan
    Duan, Qibin
    Luo, Ganfeng
    Fan, Song
    Lu, Yong
    Feng, Anping
    Zhan, Yuewei
    Liang, Bowen
    Cai, Weiping
    Zhang, Lin
    Du, Xiangjun
    Li, Linghua
    Shu, Yuelong
    Zou, Huachun
    [J]. JOURNAL OF INFECTION, 2020, 80 (06) : 656 - 665
  • [9] A tug-of-war between severe acute respiratory syndrome coronavirus 2 and host antiviral defence: lessons from other pathogenic viruses
    Fung, Sin-Yee
    Yuen, Kit-San
    Ye, Zi-Wei
    Chan, Chi-Ping
    Jin, Dong-Yan
    [J]. EMERGING MICROBES & INFECTIONS, 2020, 9 (01) : 558 - 570
  • [10] New advances in our understanding of the "unique" RNase L in host pathogen interaction and immune signaling
    Gusho, Elona
    Baskar, Danika
    Banerjee, Shuvojit
    [J]. CYTOKINE, 2020, 133