怀孕吸烟者补充维生素 C 后肺功能的改善与 5 岁时口腔 DNA 甲基化有关

IF 4.8 2区 医学 Q1 GENETICS & HEREDITY
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
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引用次数: 0

摘要

我们曾在 "维生素 C 减轻妊娠期吸烟对婴儿肺功能的影响 "随机临床试验(RCT)中报告,为妊娠期吸烟者补充维生素 C(500 毫克/天)与改善呼吸系统预后有关,而且这种改善会持续到 5 岁。本研究的目的是评估作为气道上皮替代物的口腔细胞 DNA 甲基化(DNAm)是否与补充维生素 C、肺功能改善和喘息发生率降低有关。我们使用 Infinium MethylationEPIC 阵列和口腔 DNAm 对 158 名受试者(80 名安慰剂受试者;78 名维生素 C 受试者)进行了全表观基因组关联研究(EWAS),这些受试者在 5 年访问时接受了肺功能检测(PFT)。EWAS 针对(1)维生素 C 治疗;(2)25% 至 75% 呼气量之间的用力呼气流量(FEF25-75);(3)后代喘息进行了分析。除 EWAS 中 FEF25-75 的 PFT 时的儿童身长外,模型还对性别、种族、研究地点、随机化时的胎龄(≤ OR > 18 周)、上皮细胞比例和潜在协变量进行了调整。我们将 FDR p < 0.05 视为全基因组显著性,将名义 p < 0.001 视为下游分析的候选变量。对出生时和接近 1 岁时的受试者进行口腔 DNAm 测量,以确定 DNAm 特征是起源于子宫内,还是随着年龄的增长而出现。维生素 C 治疗与 5 岁时的 457 个 FDR 显著(q < 0.05)差异甲基化 CpGs(DMCs;236 个高甲基化;221 个低甲基化)和 53 个差异甲基化区域(DMRs;26 个高甲基化;27 个低甲基化)相关。FEF25-75与一个FDR显著的DMC(cg05814800)、1,468个候选DMC(p < 0.001)和44个DMRs有关。目前的喘息与 0 个 FDR-DMC、782 个候选 DMC 和 19 个 DMRs 相关(p < 0.001)。在 365 个/457 个 5 岁维生素 C FDR 显著 DMCs 中,时间与治疗之间没有显著的交互作用。给怀孕的吸烟者补充维生素 C 与 5 岁时后代口腔 DNA 甲基化有关,而且大多数甲基化特征似乎从出生前就持续存在。5岁时的口腔甲基化还与当前的肺功能和喘息的发生有关,这些功能相关的基因位点富含维生素C相关基因位点。临床试验注册 ClinicalTrials.gov, NCT01723696 和 NCT03203603。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improvements in lung function following vitamin C supplementation to pregnant smokers are associated with buccal DNA methylation at 5 years of age
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. 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. 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. 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.
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来源期刊
自引率
5.30%
发文量
150
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
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