Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts. Harvard Medical School, Boston, Massachusetts. Meakins Christie Laboratories, McGill University Health Centre (MUHC), Montreal, Quebec, Canada.
College of Public Health and Human Sciences, Oregon State University, Corvallis.
J Gerontol A Biol Sci Med Sci. 2014 Jul;69(7):907-13. doi: 10.1093/gerona/glt179. Epub 2013 Nov 19.
A substantial proportion of the general population has low lung function, and lung function is known to decrease as we age. Low lung function is a feature of several pulmonary disorders, such as uncontrolled asthma and chronic obstructive pulmonary disease. The objective of this study is to investigate the association of polymorphisms in asthma and chronic obstructive pulmonary disease candidate genes with rates of lung function decline in a general population sample of aging men.
We analyzed data from a cohort of 1,047 Caucasian men without known lung disease, who had a mean of 25 years of lung function data, and on whom DNA was available. The cohort was randomly divided into two groups, and we tested a total of 940 single-nucleotide polymorphisms in 44 asthma and chronic obstructive pulmonary disease candidate genes in the first group (testing cohort, n = 545) for association with change in forced expiratory volume in 1 second over time.
One hundred nineteen single-nucleotide polymorphisms that showed nominal associations in the testing cohort were then genotyped and tested in the second group (replication cohort, n = 502). Evidence for association from the testing and replication cohorts were combined, and after adjustment for multiple testing, seven variants of three genes (DPP10, NPSR1, and ADAM33) remained significantly associated with change in forced expiratory volume in 1 second over time.
Our findings that genetic variants of genes involved in asthma and chronic obstructive pulmonary disease are associated with lung function decline in normal aging participants suggest that similar genetic mechanisms may underlie lung function decline in both disease and normal aging processes.
相当一部分人群的肺功能较低,且肺功能会随着年龄的增长而降低。肺功能降低是多种肺部疾病的特征之一,如未得到控制的哮喘和慢性阻塞性肺疾病。本研究旨在探究哮喘和慢性阻塞性肺疾病候选基因多态性与一般人群中老年男性肺功能下降率之间的相关性。
我们分析了一个无已知肺部疾病的 1047 名白种人男性队列的数据,这些男性的平均肺功能数据为 25 年,且有可用的 DNA。该队列被随机分为两组,我们在第一组(测试队列,n = 545)中检测了 44 个哮喘和慢性阻塞性肺疾病候选基因中的 940 个单核苷酸多态性,以评估其与 1 秒用力呼气量随时间的变化之间的相关性。
在测试队列中,有 119 个单核苷酸多态性显示出了名义上的相关性,随后在第二组(验证队列,n = 502)中进行了基因分型和测试。对测试和验证队列的证据进行了综合分析,在进行了多次检验校正后,三个基因(DPP10、NPSR1 和 ADAM33)的七个变体与 1 秒用力呼气量随时间的变化仍然显著相关。
我们的研究结果表明,参与哮喘和慢性阻塞性肺疾病的基因的遗传变异与正常衰老参与者的肺功能下降相关,这表明在疾病和正常衰老过程中,相似的遗传机制可能是肺功能下降的基础。