Tiwari Anshul, Hobbs Brian D, Sharma Rinku, Li Jiang, Kho Alvin T, Amr Sami, Celedón Juan C, Weiss Scott T, Hersh Craig P, Tantisira Kelan G, McGeachie Michael J
Channing Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA.
Respir Res. 2025 Jan 24;26(1):38. doi: 10.1186/s12931-025-03116-w.
MicroRNAs (miRNAs) are crucial post-transcriptional regulators involved in inflammatory diseases, such as asthma. Poor lung function and airflow issues in childhood are linked to the development of chronic obstructive pulmonary disease (COPD) in adulthood.
We analyzed small RNA-Seq data from 365 peripheral whole blood samples from the Genetics of Asthma in Costa Rica Study (GACRS) for association with airflow levels measured by FEV1/FVC. Differentially expressed (DE) miRNAs were identified using DESeq2 in R, adjusting for covariates and applying a 10% false discovery rate (FDR). The analysis included 361 samples and 649 miRNAs. The two DE miRNAs were further tested for association with airflow obstruction in a study of adult former smokers with and without COPD.
We found 1 upregulated and 1 downregulated miRNA in participants with airflow below the threshold compared to those above it. In the adult study, the same miRNAs were upregulated and downregulated in individuals with FEV1/FVC < 0.7 versus those with FEV1/FVC > 0.7, showing suggestive statistical evidence. The target genes of these miRNAs were enriched for PI3K-Akt, Hippo, WNT, MAPK, and focal adhesion pathways.
Two differentially expressed miRNAs were associated with airflow levels in children with asthma and airflow obstruction in adults with COPD. This suggests that shared genetic regulatory systems may influence childhood airflow and contribute to adulthood airflow obstruction.
微小RNA(miRNA)是参与炎症性疾病(如哮喘)的关键转录后调节因子。儿童期肺功能差和气流问题与成年期慢性阻塞性肺疾病(COPD)的发展有关。
我们分析了来自哥斯达黎加哮喘遗传学研究(GACRS)的365份外周全血样本的小RNA测序数据,以确定其与通过FEV1/FVC测量的气流水平的关联。使用R语言中的DESeq2软件鉴定差异表达(DE)的miRNA,对协变量进行调整并应用10%的错误发现率(FDR)。分析包括361个样本和649个miRNA。在一项针对有或没有COPD的成年前吸烟者的研究中,进一步测试了这两种DE miRNA与气流阻塞的关联。
我们发现,与气流高于阈值的参与者相比,气流低于阈值的参与者中有1种miRNA上调,1种miRNA下调。在成人研究中,与FEV1/FVC > 0.7的个体相比,FEV1/FVC < 0.7的个体中相同的miRNA上调和下调,显示出有统计学意义的证据。这些miRNA的靶基因在PI3K-Akt、Hippo、WNT、MAPK和粘着斑途径中富集。
两种差异表达的miRNA与哮喘儿童的气流水平以及COPD成人的气流阻塞有关。这表明共享的遗传调节系统可能影响儿童期气流,并导致成年期气流阻塞。