血管紧张素ii I型受体多态性(a1166c at1r)是COVID-19病程复杂化的一个因素

A.I. Vatsenko, T. Koval
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The diagnosis was made based on the examination of patients by polymerase chain reaction (PCR) and the detection of SARS-CoV-2 virus RNA in the nasopharyngeal scrapings. One of the three genotypes of the at1r gene (rs5186) was identified in each of the patients: AA, AC, and CC. The distribution of genotypes was as follows: AA - 58 people (38.4%), AC - 70 (46.4%), CC - 23 (15.2%). \nThe group of healthy individuals had the following genotype distribution: AA - 42 people (51.2%), AC - 28 people (34.1%) and SS - 12 people (14.7%). In order to determine the impact of the at1r gene polymorphism on the course of COVID-19, patients (n=151) were divided into 2 groups depending on the carriage of the C allele. \nResults: The combined AS+CC genotype was significantly more common in the group with severe (p=0.011) and severe + critical (p=0.003) course compared to the control group. 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引用次数: 0

摘要

急性呼吸道疾病COVID-19继续在全球范围内对人类健康构成威胁。确定严重冠状病毒疾病的新预测因子对于预防新的疫情和降低人群死亡率是必要的。本研究的目的是分析血管紧张素II型1受体多态性(A1166C at1r)的患病率及其对COVID-19严重程度的影响。材料与方法:我们对2020年4月至2021年3月在OR市临床机构“POKIL”和市临床机构“OR市第三医院”住院的诊断为COVID-19的151例患者进行了病例对照研究。采用聚合酶链反应(PCR)对患者进行检查,并在鼻咽刮擦物中检测SARS-CoV-2病毒RNA。at1r基因(rs5186)在AA、AC和CC 3种基因型中均有1种,基因型分布为AA - 58人(38.4%)、AC - 70人(46.4%)、CC - 23人(15.2%)。健康人群基因型分布为:AA - 42人(51.2%)、AC - 28人(34.1%)、SS - 12人(14.7%)。为了确定at1r基因多态性对COVID-19病程的影响,根据C等位基因的携带情况将患者(n=151)分为两组。结果:AS+CC联合基因型在重症组(p=0.011)和重症+危重组(p=0.003)明显高于对照组。AC+CC联合基因型患者以中度(p=0.016)、重度和危重型(p=0.016)住院的可能性显著增加。AC+CC联合基因型患者需要氧疗的可能性(67.7%)明显高于AA基因型患者(44.8%),p=0.005。他们更有可能得到口罩的支持- 49(52.7%)。结论:血管紧张素II型1受体多态性(A1166C at1r)是影响COVID-19严重程度的一个因素。合并AC+CC基因型的患者更有可能出现严重的病程并需要氧气支持。
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ANGIOTENSIN II TYPE I RECEPTOR POLYMORPHISM (A1166C AT1R) AS A FACTOR COMPLICATING THE COURSE OF COVID-19
Intriduction: The acute respiratory disease COVID-19 continues to pose a threat to human health worldwide. Identifying new predictors of severe coronavirus disease is necessary to prevent new outbreaks and reduce mortality among the population. The aim of the study was to analyze the prevalence and impact of the angiotensin II type 1 receptor polymorphism (A1166C at1r) on the severity of COVID-19. Materials and methods: We conducted a case-control study involving 151 patients who were diagnosed with COVID-19 and were inpatients at the Municipal Clinical Institution "POKIL" of the OR and the Municipal Clinical Institution "3rd City Hospital of the OR" from April 2020 to March 2021. The diagnosis was made based on the examination of patients by polymerase chain reaction (PCR) and the detection of SARS-CoV-2 virus RNA in the nasopharyngeal scrapings. One of the three genotypes of the at1r gene (rs5186) was identified in each of the patients: AA, AC, and CC. The distribution of genotypes was as follows: AA - 58 people (38.4%), AC - 70 (46.4%), CC - 23 (15.2%). The group of healthy individuals had the following genotype distribution: AA - 42 people (51.2%), AC - 28 people (34.1%) and SS - 12 people (14.7%). In order to determine the impact of the at1r gene polymorphism on the course of COVID-19, patients (n=151) were divided into 2 groups depending on the carriage of the C allele. Results: The combined AS+CC genotype was significantly more common in the group with severe (p=0.011) and severe + critical (p=0.003) course compared to the control group. Patients with combined AC+CC genotype were significantly more likely to be hospitalized with moderate (p=0.016) and severe and critical disease (p=0.016). Patients with the combined AC+CC genotype were significantly more likely to require oxygen therapy (67.7%) compared to patients with the AA genotype (44.8%), p=0.005. They were more likely to be supported with a face mask - 49 (52.7%). Conclusions: the angiotensin II type 1 receptor polymorphism (A1166C at1r) is a factor influencing the severity of COVID-19. Patients with a combined AC+CC genotype are significantly more likely to have a severe course of the disease and require oxygen support.
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