Burkart Kristin M, Manichaikul Ani, Wilk Jemma B, Ahmed Firas S, Burke Gregory L, Enright Paul, Hansel Nadia N, Haynes Demondes, Heckbert Susan R, Hoffman Eric A, Kaufman Joel D, Kurai Jun, Loehr Laura, London Stephanie J, Meng Yang, O'Connor George T, Oelsner Elizabeth, Petrini Marcy, Pottinger Tess D, Powell Charles A, Redline Susan, Rotter Jerome I, Smith Lewis J, Soler Artigas María, Tobin Martin D, Tsai Michael Y, Watson Karol, White Wendy, Young Taylor R, Rich Stephen S, Barr R Graham
For a full list of the authors' affiliations please see the Acknowledgements.
Eur Respir J. 2014 Apr;43(4):1003-17. doi: 10.1183/09031936.00147612. Epub 2013 Jul 30.
Chronic obstructive pulmonary disease (COPD) is linked to cardiovascular disease; however, there are few studies on the associations of cardiovascular genes with COPD. We assessed the association of lung function with 2100 genes selected for cardiovascular diseases among 20 077 European-Americans and 6900 African-Americans. We performed replication of significant loci in the other racial group and an independent consortium of Europeans, tested the associations of significant loci with per cent emphysema and examined gene expression in an independent sample. We then tested the association of a related lipid biomarker with forced expiratory volume in 1 s (FEV1)/forced vital capacity (FVC) ratio and per cent emphysema. We identified one new polymorphism for FEV1/FVC (rs805301) in European-Americans (p=1.3×10(-6)) and a second (rs707974) in the combined European-American and African-American analysis (p=1.38×10(-7)). Both single-nucleotide polymorphisms (SNPs) flank the gene for apolipoprotein M (APOM), a component of high-density lipoprotein (HDL) cholesterol. Both were replicated in an independent cohort. SNPs in a second gene related to apolipoprotein M and HDL, PCSK9, were associated with FEV1/FVC ratio among African-Americans. rs707974 was associated with per cent emphysema among European-Americans and African-Americans and APOM expression was related to FEV1/FVC ratio and per cent emphysema. Higher HDL levels were associated with lower FEV1/FVC ratio and greater per cent emphysema. These findings suggest a novel role for the apolipoprotein M/HDL pathway in the pathogenesis of COPD and emphysema.
慢性阻塞性肺疾病(COPD)与心血管疾病相关;然而,关于心血管基因与COPD关联的研究较少。我们在20077名欧洲裔美国人和6900名非裔美国人中评估了肺功能与2100个为心血管疾病所选基因之间的关联。我们在另一个种族群体以及一个独立的欧洲人联盟中对显著位点进行了重复验证,测试了显著位点与肺气肿百分比的关联,并在一个独立样本中检测了基因表达。然后,我们测试了一种相关脂质生物标志物与1秒用力呼气容积(FEV1)/用力肺活量(FVC)比值及肺气肿百分比之间的关联。我们在欧洲裔美国人中发现了一个新的FEV1/FVC多态性(rs805301)(p = 1.3×10⁻⁶),在欧洲裔美国人和非裔美国人的联合分析中发现了另一个(rs707974)(p = 1.38×10⁻⁷)。这两个单核苷酸多态性(SNP)都位于载脂蛋白M(APOM)基因两侧,APOM是高密度脂蛋白(HDL)胆固醇的一个组成部分。两者均在一个独立队列中得到重复验证。与载脂蛋白M和HDL相关的第二个基因PCSK9中的SNP与非裔美国人的FEV1/FVC比值相关。rs707974与欧洲裔美国人和非裔美国人的肺气肿百分比相关,且APOM表达与FEV1/FVC比值及肺气肿百分比相关。较高的HDL水平与较低的FEV1/FVC比值及较高的肺气肿百分比相关。这些发现表明载脂蛋白M/HDL途径在COPD和肺气肿发病机制中具有新作用。