Significant Association of Interleukin-6 Polymorphism and Clinical Data with COVID-19 Severity in the Southwest of Iran.

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY
Mohadeseh Sheykhi-Sabzehpoush, Ali Khodadadi, Moosa Sharifat, Maryam Haddadzadeh Shoushtari, Hanieh Raji, Ata A Ghadiri
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引用次数: 0

Abstract

Aim: Genetic predisposition is an important factor related to the enhancement of inflammation or immune responses in COVID-19 patients. This study aimed to explore the association between the IL-6 (rs1800795) polymorphism and COVID-19 severity in the southwest of Iran. Methods: We evaluated these variants in 100 patients with moderate and 100 patients with severe COVID-19 using an (Amplification Refractory Mutation System Polymerase Chain Reaction) ARMS-PCR assay. In addition, we collected clinical characteristics of patients to assess their association with the severity of COVID-19. Statistically, the significance in the present evaluation was p < 0.05. Results: Our findings showed a significant association with the SNP-174G/C of the IL-6 gene between the moderate and severe groups of COVID-19 patients under the dominant and codominant genetic models (p = 0.02 and 0.03, respectively). The frequency of the G allele was notably higher in the severe group compared to the moderate group (p = 0.02). Also, the rs1800795 genotypes, as well as the patients' age and gender (p = 0.13 and 0.31, respectively), were detected. Additionally, we confirmed a significant correlation between clinical data known as risk factors for COVID-19 severity. Conclusion: Taken together, understanding the risk factors associated with the increased severity of COVID-19 may provide the opportunity for early and useful intervention in individuals at higher risk.

伊朗西南部地区白细胞介素-6多态性和临床数据与COVID-19严重程度的显著相关性
目的:遗传易感性是COVID-19患者炎症或免疫反应增强的重要因素。本研究旨在探讨伊朗西南部地区IL-6 (rs1800795)多态性与COVID-19严重程度之间的关系。方法:我们使用(扩增难治性突变系统聚合酶链反应)ARMS-PCR方法对100例中度和100例重度COVID-19患者的这些变异进行了评估。此外,我们收集了患者的临床特征,以评估其与COVID-19严重程度的关联。统计学上,本评价的意义为p < 0.05。结果:我们的研究结果显示,在显性和共显性遗传模型下,中重度COVID-19患者IL-6基因SNP-174G/C与显性和共显性遗传模型下IL-6基因SNP-174G/C显著相关(p = 0.02和0.03)。重度组G等位基因频率明显高于中度组(p = 0.02)。检测rs1800795基因型、患者年龄和性别(p分别为0.13和0.31)。此外,我们证实了被称为COVID-19严重程度风险因素的临床数据之间存在显著相关性。综上所述,了解与COVID-19严重程度增加相关的风险因素可能为高风险个体提供早期有效干预的机会。
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来源期刊
CiteScore
2.50
自引率
7.10%
发文量
63
审稿时长
1 months
期刊介绍: Genetic Testing and Molecular Biomarkers is the leading peer-reviewed journal covering all aspects of human genetic testing including molecular biomarkers. The Journal provides a forum for the development of new technology; the application of testing to decision making in an increasingly varied set of clinical situations; ethical, legal, social, and economic aspects of genetic testing; and issues concerning effective genetic counseling. This is the definitive resource for researchers, clinicians, and scientists who develop, perform, and interpret genetic tests and their results. Genetic Testing and Molecular Biomarkers coverage includes: -Diagnosis across the life span- Risk assessment- Carrier detection in individuals, couples, and populations- Novel methods and new instrumentation for genetic testing- Results of molecular, biochemical, and cytogenetic testing- Genetic counseling
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