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Association of CRP , CD14, Pro-Inflammatory Cytokines and Their Receptors ( TNFA , LTA , TNFRSF1A , TNFRSF1B , IL1B , and IL6 ) Genes with Chronic Obstructive Pulmonary Disease Development
Russian Journal of Genetics ( IF 0.6 ) Pub Date : 2020-08-29 , DOI: 10.1134/s1022795420080086
G. F. Korytina , L. Z. Akhmadishina , O. V. Kochetova , Y. G. Aznabaeva , S. M. Izmailova , Sh. Z. Zagidullin , T. V. Victorova

The aim of the present study was to investigate the association of COPD and frequent exacerbator COPD phenotype with CRP, CD14, and pro-inflammatory cytokines and their receptors (TNFA, LTA, TNFRSF1A, TNFRSF1B, IL1B, and IL6) genes. It was found that COPD was associated with allele A of the TNFA gene (rs1800629G>A) (P = 0.002, OR = 1.45); the association was established in the log-additive model (P = 0.0022, Pcor-FDR = 0.01705, OR = 1.47); this association was confirmed in the frequent exacerbator COPD phenotype group (P = 0.001, Pcor-FDR = 0.007, OR = 1.59). Allele G of the LTA gene (rs909253A>G) (P = 0.002, OR = 1.33) was also shown to be a marker for COPD risk; the association was established in the log-additive model (P = 0.0021, Pcor-FDR = 0.01705, OR = 1.31) and it was confirmed in patients with rare exacerbations (P = 0.003, Pcor-FDR = 0.0084, OR = 1.39). The genotype GG of the TNFRSF1B gene (rs1061622T>G) was a marker of resistance to the development of the frequent exacerbator COPD phenotype (P = 0.003, Pcor-FDR = 0.0084, OR = 0.46). The genotype CC of the CD14 gene (rs2569190T>C) was associated with higher forced expiratory volume in 1 s (P = 0.006); subjects with genotype AA of the TNFRSF1B gene (rs1061624A >G) and genotype GG of the LTA gene (rs909253A>G) exhibited lower forced expiratory volume in 1 s (P = 0.04 and P = 0.01, respectively). Genotype AA of the TNFRSF1A gene (rs767455A>G) was associated with higher smoking pack-years (P = 0.0036).

中文翻译:

CRP,CD14,促炎性细胞因子及其受体(TNFA,LTA,TNFRSF1A,TNFRSF1B,IL1B和IL6)基因与慢性阻塞性肺疾病发展的关联

本研究的目的是调查慢性阻塞性肺病协会和频繁exacerbator COPD表型与CRPCD14和促炎细胞因子及其受体(TNFALTATNFRSF1ATNFRSF1BIL1BIL6)基因。据发现,COPD与等位基因相关联所述的TNFA基因(rs1800629G> A)(P = 0.002,OR = 1.45); 在对数加法模型中建立了关联(P = 0.0022,P cor-FDR= 0.01705,或= 1.47);这种关联在频繁发作的COPD表型组中得到了证实(P = 0.001,P cor-FDR = 0.007,OR = 1.59)。等位基因G ^所述的LTA基因(rs909253A> G)(P = 0.002,OR = 1.33)也证明是COPD风险的标志物; 在对数加法模型中建立了关联(P = 0.0021,P cor-FDR = 0.01705,OR = 1.31),并已在罕见急性发作患者中得到证实(P = 0.003,P cor-FDR = 0.0084,OR = 1.39) )。基因型GG的的TNFRSF1B该基因(rs1061622T> G)是对频繁发作的COPD表型发展的抗性标记(P = 0.003,P cor-FDR = 0.0084,OR = 0.46)。基因型CC的的CD14(rs2569190T> C)基因在1秒(强迫更高呼气量相关联的P = 0.006); 基因型受试者AA的的TNFRSF1B基因(rs1061624A> G)和基因型GG所述的LTA基因(rs909253A> G)在1秒(表现出较低的用力呼气量P = 0.04和P = 0.01)。基因型AA的的TNFRSF1A基因(rs767455A> G)与更高的吸烟年数相关(P = 0.0036)。
更新日期:2020-08-29
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