Epigenome-wide association study of lung function in Latino children and youth with asthma

Author:

Herrera-Luis Esther,Li Annie,Mak Angel C. Y.,Perez-Garcia Javier,Elhawary Jennifer R.,Oh Sam S.,Hu Donglei,Eng Celeste,Keys Kevin L.,Huntsman Scott,Beckman Kenneth B.,Borrell Luisa N.,Rodriguez-Santana Jose,Burchard Esteban G.,Pino-Yanes MariaORCID

Abstract

Abstract Introduction DNA methylation studies have associated methylation levels at different CpG sites or genomic regions with lung function. Moreover, genetic ancestry has been associated with lung function in Latinos. However, no epigenome-wide association study (EWAS) of lung function has been performed in this population. Here, we aimed to identify DNA methylation patterns associated with lung function in pediatric asthma among Latinos. Results We conducted an EWAS in whole blood from 250 Puerto Rican and 148 Mexican American children and young adults with asthma. A total of five CpGs exceeded the genome-wide significance threshold of p = 1.17 × 10−7 in the combined analyses from Puerto Ricans and Mexican Americans: cg06035600 (MAP3K6, p = 6.13 × 10−8) showed significant association with pre-bronchodilator Tiffeneau–Pinelli index, the probes cg00914963 (TBC1D16, p = 1.04 × 10−7), cg16405908 (MRGPRE, p = 2.05 × 10−8), and cg07428101 (MUC2, p = 5.02 × 10−9) were associated with post-bronchodilator forced vital capacity (FVC), and cg20515679 (KCNJ6) with post-bronchodilator Tiffeneau–Pinelli index (p = 1.13 × 10−8). However, these markers did not show significant associations in publicly available data from Europeans (p > 0.05). A methylation quantitative trait loci analysis revealed that methylation levels at these CpG sites were regulated by genetic variation in Latinos and the Biobank-based Integrative Omics Studies (BIOS) consortium. Additionally, two differentially methylated regions in REXOC and AURKC were associated with pre-bronchodilator Tiffeneau–Pinelli index (adjusted p < 0.05) in Puerto Ricans and Mexican Americans. Moreover, we replicated some of the previous differentially methylated signals associated with lung function in non-Latino populations. Conclusions We replicated previous associations of epigenetic markers with lung function in whole blood and identified novel population-specific associations shared among Latino subgroups.

Funder

ministerio de ciencia e innovación

Spanish ministry of universities

sandler foundation

national heart, lung, and blood institute

ucsf bakar computational health sciences institute

gordon and betty moore foundation

alfred p. sloan foundation

tobacco-related disease research program

american asthma foundation

amos medical faculty development program from the robert wood johnson foundation

harry wm. and diana v. hind distinguished professorship in pharmaceutical sciences ii

national institute of health and environmental health sciences

national institute on minority health and health disparities

the centers for common disease genomics of the genome sequencing program

national human genome research institute, the national heart, lung, and blood institute, and the national eye institute

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Developmental Biology,Genetics,Molecular Biology

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