Toll-Like Receptor (TLR2 and TLR4) Polymorphisms and Chronic Obstructive Pulmonary Disease

被引:43
|
作者
Budulac, Simona E. [1 ,5 ]
Boezen, H. Marike [1 ,5 ]
Hiemstra, Pieter S. [2 ]
Lapperre, Therese S. [2 ]
Vonk, Judith M. [1 ,5 ]
Timens, Wim [3 ,5 ]
Postma, Dirkje S. [4 ,5 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen, Netherlands
[2] Leiden Univ, Med Ctr, Dept Pulmonol, Leiden, Netherlands
[3] Univ Groningen, Dept Pathol, Univ Med Ctr Groningen, Groningen, Netherlands
[4] Univ Groningen, Dept Pulmonol, Univ Med Ctr Groningen, Groningen, Netherlands
[5] Univ Groningen, GRIAC, Univ Med Ctr Groningen, Groningen, Netherlands
来源
PLOS ONE | 2012年 / 7卷 / 08期
关键词
TOLL-LIKE-RECEPTOR-2; EXPRESSION; COPD; SALMETEROL; SMOKERS; CELLS;
D O I
10.1371/journal.pone.0043124
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
Toll-like receptors (TLRs) participate in the defence against bacterial infections that are common in patients with Chronic Obstructive Pulmonary Disease (COPD). We studied all tagging SNPs in TLR2 and TLR4 and their associations with the level and change over time of both FEV1 and sputum inflammatory cells in moderate-to-severe COPD. Nine TLR2 SNPs and 17 TLR4 SNPs were genotyped in 110 COPD patients. Associations of SNPs with lung function and inflammatory cells in induced sputum were analyzed cross-sectionally with linear regression and longitudinally with linear mixed-effect models. Two SNPs in TLR2 (rs1898830 and rs11938228) were associated with a lower level of FEV1 and accelerated decline of FEV1 and higher numbers of sputum inflammatory cells. None of the TLR4 SNPs was associated with FEV1 level. Eleven out of 17 SNPs were associated with FEV1 decline, including rs12377632 and rs10759931, which were additionally associated with higher numbers of sputum inflammatory cells at baseline and with increase over time. This is the first longitudinal study showing that tagging SNPs in TLR2 and TLR4 are associated with the level and decline of lung function as well as with inflammatory cell numbers in induced sputum in COPD patients, suggesting a role in the severity and progression of COPD.
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页数:9
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