饮食暴露、表观遗传学和青春期节奏。

IF 4.8 Q1 GENETICS & HEREDITY Environmental Epigenetics Pub Date : 2019-03-07 eCollection Date: 2019-01-01 DOI:10.1093/eep/dvz002
Yue Wu, Brisa N Sánchez, Jaclyn M Goodrich, Dana C Dolinoy, Alejandra Cantoral, Adriana Mercado-Garcia, Edward A Ruiz-Narváez, Martha M Téllez-Rojo, Karen E Peterson
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引用次数: 0

摘要

DNA 甲基化介导的基因表达变化可能在青春期节奏调节中发挥作用,而甲基供体营养素的可用性会影响这些途径。我们利用最小绝对收缩和选择算子(LASSO)研究了可能与青春期长穿插核苷酸(LINE-1)重复元素DNA甲基化相关的母体和青少年头三个月的饮食模式,并为每种模式计算了 "表观遗传学相关饮食评分"(EADS);然后测试了这些评分与青春期男孩和女孩青春期节奏的关联。分析样本包括 118 名男孩和 132 名女孩,年龄在 10-18 岁之间。对 LINE-1 重复元素的 DNA 甲基化进行了量化。利用食物频率问卷估算了母亲和青少年的典型营养摄入量。在对混杂因素进行调整后,我们分别利用医生评估的坦纳分期和自我报告的月经初潮,使用间隔删失的事件发生时间和序数回归模型来研究 EADS 分数与青春期节奏的关系。我们观察到母亲的 EADS 与青春期的开始有关联,但与青春期的进展无关。在横断面分析和前瞻性分析中,母亲EADS每增加一个标准差(SD),月经初潮推迟的几率就会增加52%(P = 0.031和0.028)。与此相反,我们观察到青春期 EADS 与青春期进展有关,但与青春期初潮无关。在男孩中,青春期 EADS 每增加一个标准差,生殖器发育较慢的几率就会增加 13%(P = 0.050),左侧和右侧睾丸发育较慢的几率也会分别增加 26% 和 27%(P = 0.001)。表观遗传相关饮食以性别和时间特异性的方式影响青春期节奏。
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Dietary exposures, epigenetics and pubertal tempo.

Gene expression changes mediated by DNA methylation may play a role in pubertal tempo regulation, and availability of methyl donor nutrients affects these pathways. We examined first trimester maternal and adolescent diet patterns that may be associated with DNA methylation at long interspersed nucleotide (LINE-1) repetitive elements in adolescence using least absolute shrinkage and selection operator (LASSO) and calculated an 'Epigenetics-Associated Diet Score' (EADS) for each pattern; then tested the associations of these scores with pubertal tempo among adolescent boys and girls. The analytic sample included 118 boys and 132 girls aged 10-18 years. DNA methylation at LINE-1 repetitive elements was quantified. Typical maternal and adolescent nutrient intakes were estimated using food frequency questionnaires. Interval-censored time to event and ordinal regression models were used to examine associations EADS scores with pubertal tempo using physician-assessed Tanner stages and self-reported menarche, respectively, adjusted for confounders. We observed associations between maternal EADS and pubertal onset, but not pubertal progression. Each standard deviation (SD) greater maternal EADS was associated with 52% higher odds of having later onset of menarche in both cross-sectional and prospective analysis (P = 0.031 and 0.028, respectively). In contrast, we observed associations between adolescent EADS and pubertal progression, but not pubertal onset. Among boys, for each SD higher adolescent EADS, there was 13% increase in odds of slower genital progression (P = 0.050), as well as 26 and 27% increase in odds of slower left and right testicular development, respectively (P = 0.001). Epigenetic-associated diet influences pubertal tempo in a sex- and timing-specific manner.

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来源期刊
Environmental Epigenetics
Environmental Epigenetics GENETICS & HEREDITY-
CiteScore
6.50
自引率
5.30%
发文量
0
审稿时长
17 weeks
期刊最新文献
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