Ash Samuel Y, Harmouche Rola, Putman Rachel K, Ross James C, Diaz Alejandro A, Hunninghake Gary M, Onieva Onieva Jorge, Martinez Fernando J, Choi Augustine M, Lynch David A, Hatabu Hiroto, Rosas Ivan O, San Jose Estepar Raul, Washko George R
Division of Pulmonary and Critical Care Medicine, Department of Medicine, Boston, MA.
Laboratory of Mathematics in Imaging, Brigham and Women's Hospital, Boston, MA.
Chest. 2017 Oct;152(4):780-791. doi: 10.1016/j.chest.2017.04.185. Epub 2017 May 12.
Smoking-related lung injury may manifest on CT scans as both emphysema and interstitial changes. We have developed an automated method to quantify interstitial changes and hypothesized that this measurement would be associated with lung function, quality of life, mortality, and a mucin 5B (MUC5B) polymorphism.
Using CT scans from the Genetic Epidemiology of COPD Study, we objectively labeled lung parenchyma as a tissue subtype. We calculated the percentage of the lung occupied by interstitial subtypes.
A total of 8,345 participants had clinical and CT scanning data available. A 5% absolute increase in interstitial changes was associated with an absolute decrease in FVC % predicted of 2.47% (P < .001) and a 1.36-point higher St. George's Respiratory Questionnaire score (P < .001). Among the 6,827 participants with mortality data, a 5% increase in interstitial changes was associated with a 29% increased risk of death (P < .001). These associations were present in a subgroup without visually defined interstitial lung abnormalities, as well as in those with normal spirometric test results, and in those without chronic respiratory symptoms. In non-Hispanic whites, for each copy of the minor allele of the MUC5B promoter polymorphism, there was a 0.64% (P < .001) absolute increase in the percentage of lung with interstitial changes.
Objective interstitial changes on CT scans were associated with impaired lung function, worse quality of life, increased mortality, and more copies of a MUC5B promoter polymorphism, suggesting that these changes may be a marker of susceptibility to smoking-related lung injury, detectable even in those who are healthy by other measures.
吸烟相关的肺损伤在CT扫描上可能表现为肺气肿和间质性改变。我们开发了一种自动方法来量化间质性改变,并假设这种测量与肺功能、生活质量、死亡率以及黏蛋白5B(MUC5B)多态性相关。
利用慢性阻塞性肺疾病(COPD)遗传流行病学研究的CT扫描,我们将肺实质客观地标记为一种组织亚型。我们计算了间质性亚型所占据的肺的百分比。
共有8345名参与者有临床和CT扫描数据。间质性改变绝对增加5%与预测的用力肺活量(FVC)百分比绝对降低2.47%相关(P <.001),以及圣乔治呼吸问卷评分高1.36分相关(P <.001)。在有死亡数据的6827名参与者中,间质性改变增加5%与死亡风险增加29%相关(P <.001)。这些关联在没有视觉上定义的间质性肺异常的亚组中存在,以及在肺活量测定测试结果正常的参与者中存在,以及在没有慢性呼吸道症状的参与者中存在。在非西班牙裔白人中,对于MUC5B启动子多态性的每个次要等位基因拷贝,间质性改变的肺的百分比绝对增加0.64%(P <.001)。
CT扫描上的客观间质性改变与肺功能受损、生活质量较差、死亡率增加以及MUC5B启动子多态性的更多拷贝相关,表明这些改变可能是对吸烟相关肺损伤易感性的一个标志物,即使在通过其他指标健康的人群中也可检测到。