Dudina K R, Kutateladze M M, Bokova N O, Znoiko O O, Abramov D D, Kelly E I, Yuschuk N D
Zh Mikrobiol Epidemiol Immunobiol. 2015 Nov-Dec(6):71-7.
Evaluate role of gene polymorphisms of surfactant proteins in susceptibility and severity of influenza infection course in representatives of Moscow population. MATERIALS AND METHODS; 320 influenza patients, infected with various influenza virus strains, and 115 healthy individuals (control group),, were included into the study. Human DNA samples genotyping for determination of SFTPA2 gene rs1965708 and rs1059046, SFTPB gene rs1130866 polymorphisms was carried out using a modified method of "adjacent samples".
Most of the individuals of the control group and influenza patients are carries of alleles and genotypes rs1965708 and rs1059046 of SFTPA2 gene, rs1130866 of SFTPB gene, that have, based on scientific literature data, shown association with severe course of influenza A(H1N1) pdm09 and other inflammatory diseases of the respiratory tract. Generally, significant differences in frequency of occurrence of unfavorable genotypes CC rs1965708, AA rs1059046 of SFTPA2 gene and CC rs1130866 of SFTPB gene in influenza patients in comparison with individuals of the control group were not detected, that gives evidence on a high (from 19 to 51%) prevalence of these genotypes in the studied population. Allele C and genotype CC rs1965708 of SFTPA2 gene, allele A and genotype AA rs1059046 of SFTPA2 gene, allele C and genotype CC rs1130866 of SFTPB gene did not shown an association with severe course of A(H1N1) pdm09 influenza. The following pathology registered in most (88%) of the patients with severe course of influenza A (H1N1)pdm09: diseases of cardiovascilar (44%), endocrine (36%) and respiratory (12%) systems.
Because in most of the deceased patients due to severe course of A (H1N1)pdm09 influenza, diseases of cardiovascular, respiratory and endocrine system were detected, and an association of unfavorable disease outcome with the studied genetic markers was not detected, dominating risk factor of development of severe course and lethal outcome for A(H1N1)pdm09 influenza in the studied cohort was comorbidity.
评估表面活性蛋白基因多态性在莫斯科人群中流感感染病程的易感性和严重程度方面的作用。材料与方法:该研究纳入了320例感染各种流感病毒株的流感患者以及115名健康个体(对照组)。采用改良的“相邻样本”方法对人类DNA样本进行基因分型,以确定SFTPA2基因的rs1965708和rs1059046、SFTPB基因的rs1130866多态性。
根据科学文献数据,对照组和流感患者中的大多数个体都是SFTPA2基因的rs1965708和rs1059046等位基因及基因型、SFTPB基因的rs1130866的携带者,这些基因已显示与甲型H1N1流感pdm09的严重病程及其他呼吸道炎症性疾病有关。总体而言,未检测到流感患者中SFTPA2基因的不利基因型CC rs1965708、AA rs1059046以及SFTPB基因的CC rs1130866的发生频率与对照组个体存在显著差异,这表明这些基因型在研究人群中的患病率较高(从19%到51%)。SFTPA2基因的等位基因C和基因型CC rs1965708、SFTPA2基因的等位基因A和基因型AA rs1059046、SFTPB基因的等位基因C和基因型CC rs1130866与甲型H1N1流感pdm09的严重病程未显示出相关性。在大多数(88%)甲型H1N1流感pdm09严重病程的患者中记录到以下病理情况:心血管系统疾病(44%)、内分泌系统疾病(36%)和呼吸系统疾病(12%)。
由于在大多数因甲型H1N1流感pdm09严重病程死亡的患者中检测到心血管、呼吸和内分泌系统疾病,且未检测到不良疾病结局与所研究的基因标记之间的关联,因此在所研究队列中,甲型H1N1流感pdm09严重病程和致死结局的主要危险因素是合并症。