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COVID-19 susceptibility: potential of polymorphisms.新冠病毒易感性:多态性的可能性
Egypt J Med Hum Genet. 2020;21(1):54. doi: 10.1186/s43042-020-00099-9. Epub 2020 Sep 21.
2
Fast evolution of SARS-CoV-2 BA.2.86 to JN.1 under heavy immune pressure.在强大免疫压力下,新冠病毒BA.2.86快速进化为JN.1 。
Lancet Infect Dis. 2024 Feb;24(2):e70-e72. doi: 10.1016/S1473-3099(23)00744-2. Epub 2023 Dec 15.
3
Its all about IFN-λ4: Protective role of IFNL4 polymorphism against COVID-19-related pneumonia in females.全因 IFN-λ4:IFNL4 多态性对女性 COVID-19 相关肺炎的保护作用。
J Med Virol. 2023 Oct;95(10):e29152. doi: 10.1002/jmv.29152.
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'The end' - or is it? Emergence of SARS-CoV-2 EG.5 and BA.2.86 subvariants.“结束”——真的是这样吗?新型冠状病毒奥密克戎变异株EG.5和BA.2.86的出现。
Future Virol. 2023 Sep. doi: 10.2217/fvl-2023-0150. Epub 2023 Sep 19.
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Severity of SARS-CoV-2 Omicron XBB subvariants in Singapore.新加坡新冠病毒奥密克戎XBB亚变体的严重程度。
Lancet Reg Health West Pac. 2023 Jul 25;37:100849. doi: 10.1016/j.lanwpc.2023.100849. eCollection 2023 Aug.
6
Association between angiotensin-converting enzyme-2 gene polymorphism (rs2106809) with severity and outcome of COVID-19 infection.血管紧张素转换酶 2 基因多态性(rs2106809)与 COVID-19 感染严重程度和结局的关系。
Mol Biol Rep. 2023 Aug;50(8):6669-6679. doi: 10.1007/s11033-023-08493-3. Epub 2023 Jun 27.
7
Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity.分析 ACE2、AR、MX1 和 TMPRSS2 遗传标志物在 COVID-19 严重程度中的作用。
Hum Genomics. 2023 Jun 7;17(1):50. doi: 10.1186/s40246-023-00496-2.
8
Demographic, clinical and genetic factors associated with COVID-19 disease susceptibility and mortality in a Kurdish population.与库尔德人群 COVID-19 易感性和死亡率相关的人口统计学、临床和遗传因素。
Ann Saudi Med. 2023 May-Jun;43(3):125-142. doi: 10.5144/0256-4947.2023.125. Epub 2023 Jun 1.
9
End of COVID-19 emergencies sparks debate.新冠大流行紧急状态结束引发争论。
Science. 2023 May 12;380(6645):566-567. doi: 10.1126/science.adi6511. Epub 2023 May 11.
10
Diagnostic accuracy of a set of clinical and radiological criteria for screening of COVID-19 using RT-PCR as the reference standard.使用 RT-PCR 作为参考标准的一组临床和影像学标准对 COVID-19 进行筛查的诊断准确性。
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以及基因多态性作为女性新冠病毒疾病严重程度和预后的潜在预测指标。

and genetic polymorphisms as potential predictors of COVID-19 severity and outcome in females.

作者信息

Matic Sanja, Milovanovic Dragan, Mijailovic Zeljko, Djurdjevic Predrag, Stefanovic Srdjan, Todorovic Danijela, Vitosevic Katarina, Canovic Vanja, Popovic Suzana, Dimitrijevic Nevena Milivojevic, Zivanovic Marko, Seklic Dragana, Aleksic Sanja, Djordjevic Nemanja, Vukic Milena, Vukovic Nenad, Filipovic Nenad, Baskic Dejan, Djordjevic Natasa

机构信息

Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.

Department of Pharmacology and Toxicology, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.

出版信息

Front Med (Lausanne). 2024 Dec 18;11:1493815. doi: 10.3389/fmed.2024.1493815. eCollection 2024.

DOI:10.3389/fmed.2024.1493815
PMID:39744525
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11688283/
Abstract

INTRODUCTION

ACE2 and TMPRSS2 represent the major gateways for SARS-CoV-2 cell entry. The presence of functional ACE2 and TMPRSS2 genetic polymorphisms that affect gene expression may affect the risk of severe form of COVID-19 and its fatal outcome.

MATERIAL AND PATIENTS

This observational study enrolled 178 hospitalized patients diagnosed with SARS-CoV-2 infection at the University Clinical Centre of Kragujevac, Serbia. Demographic, clinical, and laboratory data were gathered at admission. Genotyping for single nucleotide polymorphisms of (rs2106809 and rs2074192) and (rs2070788 and rs4818239) was performed using the Real-Time PCR method with TaqMan assays.

RESULTS

Controlling for other factors of influence, such as CCI, N/L ratio, LDH level, and pO, we showed that females with rs2070788 A/A genotype were less likely to develop severe COVID-19 (odds ratio [OR] [95% confidence interval (95% CI)]: 0.030 [0.001; 0.862]). Additionally, the likelihood of dying of SARS-CoV-2 infection was lower in female carriers of at least one rs2106809 C allele (OR [95% CI]: 0.004 [0.000; 0.981]).

CONCLUSION

Our findings indicate rs2070788 and rs2106809 polymorphisms as independent predictors of severity and outcome of COVID-19 in females.

摘要

引言

血管紧张素转换酶2(ACE2)和跨膜丝氨酸蛋白酶2(TMPRSS2)是严重急性呼吸综合征冠状病毒2(SARS-CoV-2)进入细胞的主要途径。影响基因表达的功能性ACE2和TMPRSS2基因多态性的存在可能会影响重症新型冠状病毒肺炎(COVID-19)的风险及其致命结局。

材料与患者

本观察性研究纳入了塞尔维亚克拉古耶瓦茨大学临床中心178例被诊断为SARS-CoV-2感染的住院患者。入院时收集人口统计学、临床和实验室数据。使用TaqMan分析法的实时聚合酶链反应(PCR)方法对ACE2(rs2106809和rs2074192)和TMPRSS2(rs2070788和rs4818239)的单核苷酸多态性进行基因分型。

结果

在控制其他影响因素,如Charlson合并症指数(CCI)、中性粒细胞/淋巴细胞比值(N/L)、乳酸脱氢酶(LDH)水平和动脉血氧分压(pO)后,我们发现携带TMPRSS2 rs2070788 A/A基因型的女性发生重症COVID-19的可能性较小(优势比[OR][95%置信区间(95%CI)]:0.030[0.001;0.862])。此外,至少携带一个ACE2 rs2106809 C等位基因的女性死于SARS-CoV-2感染的可能性较低(OR[95%CI]:0.004[(0.000;0.9"

结论

我们的研究结果表明,TMPRSS2 rs2070788和ACE2 rs2106809多态性是女性COVID-19严重程度和结局的独立预测因素。 81])。