Li Minjing, Cai Wanru, Chen Ye, Dong Lei
Department of Pneumology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Genet Test Mol Biomarkers. 2019 Sep;23(9):634-643. doi: 10.1089/gtmb.2019.0053. Epub 2019 Aug 6.
Caveolin-1, which is encoded by the caveolin-1 () gene, plays an important role in the development of pulmonary hypertension (PH). The purpose of this study was to determine the relationship between 3' untranslated region (UTR) single nucleotide polymorphisms (SNPs) of the gene and the risk of PH in Chinese Han patients with chronic obstructive pulmonary disease (COPD). From March 2016 to October 2018, 235 patients with COPD combined with PH (COPD/PH) and 240 patients with COPD and without PH (COPD/PH) were recruited to the study. The gene rs1049314, rs8713, rs1049334, rs6867, and rs1049337 loci were genotyped and the plasma hsa-miR-451 and caveolin-1 levels were measured in all subjects. The risk of PH in patients with COPD carrying the C allele of the rs8713 locus was 2.82 times higher than that in A allele carriers (95% confidence interval [CI], 1.94-4.08; < 0.001). The risk of PH in patients with COPD carrying the T allele of the rs1049337 locus was significantly lower than that in C allele carriers (odds ratio [OR], 0.48; 95% CI, 0.37-0.63; < 0.001). The ACGAC haplotype was found to be a highly-significant risk factor for COPD combined with PH (OR, 2.24; 95% CI, 1.20-4.17; = 0.01). Plasma levels of hsa-miR-451 and the caveolin1 protein in patients with the rs8713 C allele were significantly lower than in those with the wild type (WT) allele regardless of PH status. Conversely, the hsa-miRN-451 and caveolin-1 levels in patients with the rs1049337 mutant C allele were significantly higher than those in the WT T allele ( < 0.05). There was a positive correlation between plasma hsa-miR-451 and caveolin-1 levels in patients with COPD/PH and COPD/PH ( = 0.72 and 0.63, respectively). SNPs of the gene loci rs8713 and rs1049337 are associated with a risk of PH in COPD patients. The underlying mechanism is likely to be related to the effect of the SNPs on the regulation of caveolin-1 by hsa-miR-451.
小窝蛋白-1由小窝蛋白-1(CAV1)基因编码,在肺动脉高压(PH)的发生发展中起重要作用。本研究旨在确定CAV1基因3'非翻译区(UTR)单核苷酸多态性(SNP)与中国汉族慢性阻塞性肺疾病(COPD)患者发生PH风险之间的关系。2016年3月至2018年10月,本研究招募了235例COPD合并PH(COPD/PH)患者和240例COPD但无PH(COPD/非PH)患者。对所有受试者的CAV1基因rs1049314、rs8713、rs1049334、rs6867和rs1049337位点进行基因分型,并检测血浆hsa-miR-451和小窝蛋白-1水平。携带rs8713位点C等位基因的COPD患者发生PH的风险比携带A等位基因的患者高2.82倍(95%置信区间[CI],1.94 - 4.08;P<0.001)。携带rs1049337位点T等位基因的COPD患者发生PH的风险显著低于携带C等位基因的患者(优势比[OR],0.48;95% CI,0.37 - 0.63;P<0.001)。发现ACGAC单倍型是COPD合并PH的高度显著危险因素(OR,2.24;95% CI,1.20 - 4.17;P = 0.01)。无论PH状态如何;携带rs8713 C等位基因的患者血浆hsa-miR-451和小窝蛋白1蛋白水平均显著低于野生型(WT)等位基因患者。相反,携带rs1049337突变C等位基因的患者hsa-miRN-451和小窝蛋白-1水平显著高于WT T等位基因患者(P<0.05)。COPD/PH和COPD/非PH患者血浆hsa-miR-451和小窝蛋白-1水平呈正相关(分别为r = 0.72和0.63)。CAV1基因位点rs8713和rs1049337的SNP与COPD患者发生PH的风险相关。潜在机制可能与SNP对hsa-miR-451调节小窝蛋白-1的作用有关。