HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico.
Tobacco Smoking and COPD Research Department, Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas, Mexico City 14080, Mexico.
Curr Issues Mol Biol. 2021 Aug 3;43(2):887-899. doi: 10.3390/cimb43020063.
Chronic Obstructive Pulmonary Disease (COPD) is an inflammatory disease characterized by airflow obstruction, commonly present in smokers and subjects exposed to noxious particles product of biomass-burning smoke (BBS). Several association studies have identified single-nucleotide polymorphisms (SNP) in coding genes related to the heat shock proteins family-genes that codify the heat shock proteins (Hsp). Hsp accomplishes critical roles in regulating immune response, antigen-processing, eliminating protein aggregates and co-activating receptors. The presence of SNPs in these genes can lead to alterations in immune responses. We aimed to evaluate the association of SNPs in the HSP90 gene complex and COPD.
We enrolled 1549 participants, divided into two comparison groups; 919 tobacco-smoking subjects (cases COPD-TS n = 294 and, controls SWOC n = 625) and 630 chronic exposed to BBS (cases COPD-BBS n = 186 and controls BBES n = 444). We genotyped 2 SNPs: the rs13296 in and rs2070908 in .
Through the dominant model (GC + CC), the rs2070908 is associated with decreased risk ( < 0.01, OR = 0.6) to suffer COPD among chronic exposed BBS subjects. We found an association between rs13296 GG genotype and lower risk ( = 0.01, OR = 0.22) to suffer severe COPD-TS forms in the severity analysis.
single-nucleotide variants in the and genes are associated with decreased COPD risk in subjects exposed to BBS and the most severe forms of COPD in tobacco-smoking subjects.
慢性阻塞性肺疾病(COPD)是一种以气流受限为特征的炎症性疾病,常见于吸烟者和暴露于生物量燃烧烟雾(BBS)有害颗粒产物的人群。几项关联研究已经确定了与热休克蛋白家族相关的编码基因中的单核苷酸多态性(SNP)-编码热休克蛋白(Hsp)的基因。Hsp 在调节免疫反应、抗原处理、消除蛋白质聚集和共激活受体方面发挥着关键作用。这些基因中的 SNP 的存在可能导致免疫反应的改变。我们旨在评估 HSP90 基因复合物中 SNP 与 COPD 的关联。
我们纳入了 1549 名参与者,分为两组比较;919 名吸烟人群(病例 COPD-TS n = 294,对照组 SWOC n = 625)和 630 名慢性暴露于 BBS 的人群(病例 COPD-BBS n = 186,对照组 BBES n = 444)。我们对 2 个 SNP 进行了基因分型: 中的 rs13296 和 中的 rs2070908。
通过显性模型(GC + CC),rs2070908 与慢性暴露于 BBS 的人群中 COPD 风险降低(<0.01,OR = 0.6)相关。在严重程度分析中,我们发现 rs13296 GG 基因型与严重 COPD-TS 形式的较低风险(=0.01,OR = 0.22)相关。
基因和 基因中的单核苷酸变体与暴露于 BBS 的人群中 COPD 风险降低以及吸烟人群中 COPD 最严重形式相关。