Association Between IL-1A Single Nucleotide Polymorphisms and Chronic Beryllium Disease and Beryllium Sensitization

被引:4
|
作者
McCanlies, Erin C. [1 ]
Yucesoy, Berran [1 ]
Mnatsakanova, Anna [1 ]
Slaven, James E. [1 ]
Andrew, Michael [1 ]
Frye, Bonnie L. [1 ]
Schuler, Christine R. [2 ]
Kreiss, Kathleen [2 ]
Weston, Ainsley [2 ]
机构
[1] NIOSH, Hlth Effects Lab Div, Ctr Dis Control & Prevent, CDC, Morgantown, WV 26505 USA
[2] NIOSH, Div Resp Dis Studies, Ctr Dis Control & Prevent, CDC, Morgantown, WV 26505 USA
关键词
IDIOPATHIC PULMONARY FIBROSIS; NECROSIS-FACTOR-ALPHA; MHC-CLASS-II; ALVEOLAR MACROPHAGES; GENE POLYMORPHISMS; SARCOIDOSIS; CYTOKINE; RISK; SUSCEPTIBILITY; HLA-DPB1;
D O I
10.1097/JOM.0b013e3181e48ec8
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objective: To determine if single nucleotide polymorphisms (SNPs) in interleukin (IL) IL-1A, IL-1B, IL-1RN, IL-2, IL-9, and IL-9R were associated with chronic beryllium disease (CBD) and beryllium sensitization (BeS). Methods: Forty SNPs in six IL genes were evaluated in 85 individuals with CBD, 61 individuals with BeS, and 730 individuals without BeS or CBD (nonsensitized) using a 5' nuclease polymerase chain reaction assay. Logistic regression was used to evaluate the association between IL SNPs, CBD, and BeS, adjusting for plant-site and HLA-DPB1(Glu69) in additive, dominant, and recessive inheritance models. Results: IL-1A-1142, IL-1A-3769, and IL-1A-4697 were significantly associated with CBD in both the additive and dominant models compared to individuals with BeS or the nonsensitized. Conclusions: These results indicate that genetic variations in the IL-1A gene may play a role in the development of CBD but not BeS.
引用
收藏
页码:680 / 684
页数:5
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