Obeidat Ma'en, Fishbane Nick, Nie Yunlong, Chen Virginia, Hollander Zsuzsanna, Tebbutt Scott J, Bossé Yohan, Ng Raymond T, Miller Bruce E, McManus Bruce, Rennard Stephen, Paré Peter D, Sin Don D
The University of British Columbia Centre for Heart Lung Innovation, St Paul's Hospital, Vancouver, BC, Canada.
Prevention of Organ Failure (PROOF) Centre of Excellence, Vancouver, BC, Canada.
PLoS One. 2015 Oct 13;10(10):e0140022. doi: 10.1371/journal.pone.0140022. eCollection 2015.
COPD is currently the fourth leading cause of death worldwide. Statins are lipid lowering agents with documented cardiovascular benefits. Observational studies have shown that statins may have a beneficial role in COPD. The impact of statins on blood gene expression from COPD patients is largely unknown.
Identify blood gene signature associated with statin use in COPD patients, and the pathways underpinning this signature that could explain any potential benefits in COPD.
Whole blood gene expression was measured on 168 statin users and 451 non-users from the ECLIPSE study using the Affymetrix Human Gene 1.1 ST microarray chips. Factor Analysis for Robust Microarray Summarization (FARMS) was used to process the expression data. Differential gene expression analysis was undertaken using the Linear Models for Microarray data (Limma) package adjusting for propensity score and surrogate variables. Similarity of the expression signal with published gene expression profiles was performed in ProfileChaser.
25 genes were differentially expressed between statin users and non-users at an FDR of 10%, including LDLR, CXCR2, SC4MOL, FAM108A1, IFI35, FRYL, ABCG1, MYLIP, and DHCR24. The 25 genes were significantly enriched in cholesterol homeostasis and metabolism pathways. The resulting gene signature showed correlation with Huntington's disease, Parkinson's disease and acute myeloid leukemia gene signatures.
The blood gene signature of statins' use in COPD patients was enriched in cholesterol homeostasis pathways. Further studies are needed to delineate the role of these pathways in lung biology.
慢性阻塞性肺疾病(COPD)目前是全球第四大致死原因。他汀类药物是具有心血管益处记录的降脂药物。观察性研究表明,他汀类药物可能在COPD中发挥有益作用。他汀类药物对COPD患者血液基因表达的影响在很大程度上尚不清楚。
确定与COPD患者使用他汀类药物相关的血液基因特征,以及支撑该特征的通路,这些通路可以解释在COPD中的任何潜在益处。
使用Affymetrix Human Gene 1.1 ST微阵列芯片,对ECLIPSE研究中的168名他汀类药物使用者和451名非使用者进行全血基因表达测量。使用稳健微阵列汇总因子分析(FARMS)处理表达数据。使用微阵列数据线性模型(Limma)软件包进行差异基因表达分析,并对倾向得分和替代变量进行调整。在ProfileChaser中进行表达信号与已发表基因表达谱的相似性分析。
在错误发现率为10%时,他汀类药物使用者和非使用者之间有25个基因差异表达,包括低密度脂蛋白受体(LDLR)、趋化因子受体2(CXCR2)、鞘氨醇4-单加氧酶(SC4MOL)、家族性108A1(FAM108A1)、干扰素诱导蛋白35(IFI35)、Fry样蛋白(FRYL)、ATP结合盒转运蛋白G1(ABCG1)、微粒体甘油三酯转运蛋白(MYLIP)和二氢胆固醇还原酶24(DHCR24)。这25个基因在胆固醇稳态和代谢通路中显著富集。所得基因特征与亨廷顿舞蹈病、帕金森病和急性髓系白血病基因特征相关。
COPD患者使用他汀类药物的血液基因特征在胆固醇稳态通路中富集。需要进一步研究来阐明这些通路在肺生物学中的作用。