Polymorphisms in Inflammasome Genes and Risk of Coal Workers' Pneumoconiosis in a Chinese Population

被引:33
|
作者
Ji, Xiaoming [1 ]
Hou, Zhiguo [1 ]
Wang, Ting [1 ]
Jin, Kexin [1 ]
Fan, Jingjing [1 ]
Luo, Chen [1 ]
Chen, Minjuan [1 ]
Han, Ruhui [1 ]
Ni, Chunhui [1 ]
机构
[1] Nanjing Med Univ, Sch Publ Hlth, Dept Occupat Med & Environm Hlth, Nanjing, Jiangsu, Peoples R China
来源
PLOS ONE | 2012年 / 7卷 / 10期
基金
中国国家自然科学基金;
关键词
NOD-LIKE PROTEINS; NALP3; INFLAMMASOME; NLRP3; ASSOCIATION; FIBROSIS; DISEASE; INTERLEUKIN-1-BETA; EXPRESSION; SILICOSIS; SEVERITY;
D O I
10.1371/journal.pone.0047949
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Coal workers' pneumoconiosis (CWP), resulting from the inhalation of silica-containing coal mine dust, is characterized by fibrosing nodular lesions that eventually develop into progressive pulmonary fibrosis. Recently, it has been hypothesized that inflammasomes could have a crucial role in the host response to silica and recent studies show that the inflammasome contributes to inflammation and pulmonary fibrosis. NLRP3, CARD8 are components of the NLRP3 inflammasome, which triggers caspase 1-mediated IL-1 beta and IL-18 release. In the present study, we investigated whether common single nucleotide polymorphisms (SNPs) in inflammasome genes are associated with CWP. Methods: We performed an association study analyzing 3 NLRP3, 1 CARD8, 1 IL-1 beta, 2 IL-18 SNPs in a case-control study of 697 CWP and 694 controls. Genotyping was carried out by the TaqMan method. Results: The NLRP3 rs1539019 TT genotype was associated with a significantly increased risk of CWP (adjusted odds ratio (OR) = 1.39, 95% confidence interval (CI) = 1.07-1.81), compared with the GG/GT genotype, in particular among smokers (adjusted OR = 1.67, 95% CI = 1.15-2.42). In addition, the polymorphism was significantly associated with risk of CWP patients with stage I. Conclusions: This is the first report showing an association between the NLRP3 rs1539019 polymorphism and CWP, and suggests that this polymorphism may confer increased risk for the development of the disease. Further studies are warranted to confirm our findings.
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页数:7
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