Channing Division of Network Medicine and.
National Jewish Health, Denver, Colorado.
Am J Respir Crit Care Med. 2020 May 1;201(9):1099-1109. doi: 10.1164/rccm.201902-0439OC.
Smoking results in at least a decade lower life expectancy. Mortality among current smokers is two to three times as high as never smokers. DNA methylation is an epigenetic modification of the human genome that has been associated with both cigarette smoking and mortality. We sought to identify DNA methylation marks in blood that are predictive of mortality in a subset of the COPDGene (Genetic Epidemiology of COPD) study, representing 101 deaths among 667 current and former smokers. We assayed genome-wide DNA methylation in non-Hispanic white smokers with and without chronic obstructive pulmonary disease (COPD) using blood samples from the COPDGene enrollment visit. We tested whether DNA methylation was associated with mortality in models adjusted for COPD status, age, sex, current smoking status, and pack-years of cigarette smoking. Replication was performed in a subset of 231 individuals from the ECLIPSE (Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints) study. We identified seven CpG sites associated with mortality (false discovery rate < 20%) that replicated in the ECLIPSE cohort ( < 0.05). None of these marks were associated with longitudinal lung function decline in survivors, smoking history, or current smoking status. However, differential methylation of two replicated (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta) sites were associated with lung function at enrollment ( < 0.05). We also observed associations between DNA methylation and gene expression for the sites. This study is the first to identify variable DNA methylation associated with all-cause mortality in smokers with and without COPD. Evaluating predictive epigenomic marks of smokers in peripheral blood may allow for targeted risk stratification and aid in delivery of future tailored therapeutic interventions.
吸烟会导致预期寿命至少缩短十年。目前吸烟者的死亡率是从不吸烟者的两到三倍。DNA 甲基化是人类基因组的一种表观遗传修饰,与吸烟和死亡率都有关。我们试图在 COPDGene(COPD 的遗传流行病学)研究的一个亚组中确定血液中与死亡率相关的 DNA 甲基化标记,该亚组代表了 667 名目前和以前的吸烟者中的 101 例死亡。我们使用 COPDGene 登记访问时的血液样本,对无西班牙裔白人吸烟者进行了有无慢性阻塞性肺疾病(COPD)的全基因组 DNA 甲基化检测。我们测试了在调整 COPD 状态、年龄、性别、当前吸烟状态和吸烟包年数的模型中,DNA 甲基化是否与死亡率相关。在 ECLIPSE(评估 COPD 纵向以确定预测替代终点)研究的一个 231 人的亚组中进行了复制。我们确定了七个与死亡率相关的 CpG 位点(错误发现率 < 20%),在 ECLIPSE 队列中得到了复制( < 0.05)。这些标记都与幸存者的纵向肺功能下降、吸烟史或当前吸烟状态无关。然而,两个复制的(磷脂酰肌醇-4,5-二磷酸 3-激酶催化亚基 delta)位点的差异甲基化与入组时的肺功能有关( < 0.05)。我们还观察到 DNA 甲基化与基因表达之间的关联。这项研究首次在有和没有 COPD 的吸烟者中发现了与全因死亡率相关的可变 DNA 甲基化。评估吸烟者外周血中预测性表观遗传标记可能允许进行有针对性的风险分层,并有助于提供未来的定制治疗干预。