A genome-wide study of DNA methylation in white blood cells and asthma in Latino children and youth. Issue 5 (4th May 2021)

• Record Type: Journal Article
• Authors: Jiang, Yale; Forno, Erick; Han, Yueh-Ying; Xu, Zhongli; Hu, Donglei; Boutaoui, Nadia; Eng, Celeste; Acosta-Pérez, Edna; Huntsman, Scott; Colón-Semidey, Angel; Keys, Kevin L.; Rodríguez-Santana, José R.; Alvarez, María; Pino-Yanes, Maria; Canino, Glorisa; Chen, Wei; Burchard, Esteban G.; Celedón, Juan C.
• Is Part Of: Epigenetics. Volume 16:Issue 5(2021)
• Page Start: 577
• Page End: 585
• Publication Date: 2021-05-04
• Subjects: Asthma -- epigenome-wide -- DNA methylation -- white blood cells; Epigenesis -- Periodicals; Epigenetica; 572.86505
• DOI: 10.1080/15592294.2020.1809872
• Languages: English
• ISSNs: 1559-2294

Abstract

ABSTRACT: Latinos are heavily affected with childhood asthma. Little is known about epigenetic mechanisms of asthma in Latino youth. We conducted a meta-analysis of two epigenome-wide association studies (EWAS) of asthma, using DNA from white blood cells (WBCs) from 1, 136 Latino children and youth aged 6 to 20 years. Genes near the top CpG sites in this EWAS were examined in a pathway enrichment analysis, and we then assessed whether our results replicated those from publicly available data from three independent EWAS conducted in non-Latino populations. We found that DNA methylation profiles differed between subjects with and without asthma. After adjustment for covariates and multiple testing, two CpGs were differentially methylated at a false discovery rate (FDR)-adjusted P < 0.1, and 193 CpG sites were differentially methylated at FDR-adjusted P < 0.2. The two top CpGs are near genes relevant to inflammatory signalling, including CAMK1D (Calcium/Calmodulin Dependent Protein Kinase ID) and TIGIT (T Cell Immunoreceptor With Ig And ITIM Domains). Moreover, 25 genomic regions were differentially methylated between subjects with and without asthma, at Šidák-corrected P < 0.10. An enrichment analysis then identified the TGF-beta pathway as most relevant to asthma in our analysis, and we replicated some of the top signals from publicly available EWAS datasets in non-Hispanic populations. In conclusion, we have identified novel epigenetic markers of asthma in WBCs from Latino children and youth, while also replicating previous results from studies conducted in non-Latinos.