首页    期刊浏览 2024年12月04日 星期三
登录注册

文章基本信息

  • 标题:Susceptibility loci in lung cancer and COPD: association of IREB2 and FAM13A with pulmonary diseases
  • 本地全文:下载
  • 作者:Iwona Ziółkowska-Suchanek ; Maria Mosor ; Piotr Gabryel
  • 期刊名称:Scientific Reports
  • 电子版ISSN:2045-2322
  • 出版年度:2015
  • 卷号:5
  • DOI:10.1038/srep13502
  • 出版社:Springer Nature
  • 摘要:Genome-wide association studies have identified loci at 15q25 ( IREB2 ) and 4q22 ( FAM13A ), associated with lung cancer (LC) and chronic obstructive pulmonary disease (COPD). The aim of our research was to determine the association of IREB2 and FAM13A SNPs with LC and severe/very severe COPD patients. We examined IREB2 variants (rs2568494, rs2656069, rs10851906, rs13180) and FAM13A (rs1903003, rs7671167, rs2869967) among 1.141 participants (468 LC, 149 COPD, 524 smoking controls). The frequency of the minor IREB2 rs2568494 AA genotype, was higher in LC vs controls ( P = 0.0081, OR = 1.682). The FAM13A rs2869967 was associated with COPD (minor CC genotype: P = 0.0007, OR = 2.414). The rs1903003, rs7671167 FAM13A variants confer a protective effect on COPD (both P IREB2 AAAT haplotype with LC ( P = 0.0021, OR = 1.513) and FAM13A TTC with COPD ( P = 0.0013, OR = 1.822). Cumulative genetic risk score analyses (CGRS), derived by adding risk alleles, revealed that the risk for COPD increased with the growing number of the FAM13A risk alleles. OR (95% CI) for carriers of ≥5 risk alleles reached 2.998 (1.8 to 4.97) compared to the controls. This study confirms that the IREB2 variants contribute to an increased risk of LC, whereas FAM13A predisposes to increased susceptibility to COPD.
国家哲学社会科学文献中心版权所有