Improvements in lung function following vitamin C supplementation to pregnant smokers are associated with buccal DNA methylation at 5 years of age (vol 16, 10.1186/s13148-024-01644-8, 2024)

被引:0
|
作者
Shorey-Kendrick, Lyndsey E. [1 ]
Mcevoy, Cindy T. [2 ]
Milner, Kristin [3 ]
Harris, Julia [3 ]
Brownsberger, Julie [3 ]
Tepper, Robert S. [4 ]
Park, Byung [5 ]
Gao, Lina [5 ]
Vu, Annette [6 ,7 ]
Morris, Cynthia D. [6 ,7 ]
Spindel, Eliot R. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Oregon Natl Primate Res Ctr, Div Neurosci, Beaverton, OR 97006 USA
[2] Oregon Hlth & Sci Univ, Pape Pediat Res Inst, Dept Pediat, Portland, OR USA
[3] Oregon Hlth & Sci Univ, Dept Pediat, Portland, OR USA
[4] Indiana Univ Sch Med, Herman B Wells Ctr Pediat Res, Dept Pediat, Indianapolis, IN USA
[5] Portland State Univ, Oregon Hlth & Sci Univ, Knight Canc Inst, Oregon Natl Primate Res Ctr,Sch Publ Hlth,Biostat, Portland, OR USA
[6] Oregon Clin & Translat Res Inst, Oregon Hlth & Sci, Portland, OR USA
[7] Oregon Hlth & Sci Univ, Dept Med Informat & Clin Epidemiol, Portland, OR USA
关键词
Airway; DNA methylation; Lung function; MethylationEPIC; MSDP: maternal smoking during pregnancy; Nicotine; RCT: randomized clinical trial; Vitamin C; Wheeze;
D O I
10.1186/s13148-024-01664-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: We previously reported in the “Vitamin C to Decrease the Effects of Smoking in Pregnancy on Infant Lung Function” randomized clinical trial (RCT) that vitamin C (500 mg/day) supplementation to pregnant smokers is associated with improved respiratory outcomes that persist through 5 years of age. The objective of this study was to assess whether buccal cell DNA methylation (DNAm), as a surrogate for airway epithelium, is associated with vitamin C supplementation, improved lung function, and decreased occurrence of wheeze. Methods: We conducted epigenome-wide association studies (EWAS) using Infinium MethylationEPIC arrays and buccal DNAm from 158 subjects (80 placebo; 78 vitamin C) with pulmonary function testing (PFT) performed at the 5-year visit. EWAS were performed on (1) vitamin C treatment, (2) forced expiratory flow between 25 and 75% of expired volume (FEF25–75), and (3) offspring wheeze. Models were adjusted for sex, race, study site, gestational age at randomization (≤ OR > 18 weeks), proportion of epithelial cells, and latent covariates in addition to child length at PFT in EWAS for FEF25–75. We considered FDR p < 0.05 as genome-wide significant and nominal p < 0.001 as candidates for downstream analyses. Buccal DNAm measured in a subset of subjects at birth and near 1 year of age was used to determine whether DNAm signatures originated in utero, or emerged with age. Results: Vitamin C treatment was associated with 457 FDR significant (q < 0.05) differentially methylated CpGs (DMCs; 236 hypermethylated; 221 hypomethylated) and 53 differentially methylated regions (DMRs; 26 hyper; 27 hypo) at 5 years of age. FEF25–75 was associated with one FDR significant DMC (cg05814800), 1,468 candidate DMCs (p < 0.001), and 44 DMRs. Current wheeze was associated with 0 FDR-DMCs, 782 candidate DMCs, and 19 DMRs (p < 0.001). In 365/457 vitamin C FDR significant DMCs at 5 years of age, there was no significant interaction between time and treatment. Conclusions: Vitamin C supplementation to pregnant smokers is associated with buccal DNA methylation in offspring at 5 years of age, and most methylation signatures appear to be persistent from the prenatal period. Buccal methylation at 5 years was also associated with current lung function and occurrence of wheeze, and these functionally associated loci are enriched for vitamin C associated loci. Clinical trial registration ClinicalTrials.gov, NCT01723696 and NCT03203603. © The Author(s) 2024.
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  • [1] Improvements in lung function following vitamin C supplementation to pregnant smokers are associated with buccal DNA methylation at 5 years of age
    Lyndsey E. Shorey-Kendrick
    Cindy T. McEvoy
    Kristin Milner
    Julia Harris
    Julie Brownsberger
    Robert S. Tepper
    Byung Park
    Lina Gao
    Annette Vu
    Cynthia D. Morris
    Eliot R. Spindel
    Clinical Epigenetics, 16