新生儿DNA甲基化年龄区分长期体重轨迹:波士顿出生队列
Anat Yaskolka Meir1, Guoying Wang2, Xiumei Hong2
1Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA.
BMC medicine
|September 10, 2024
概括
新生儿DNA甲基化年龄 (GAmAge) 预测了长期儿童超重或肥胖 (OWO) 轨迹,独立于妊娠年龄. 这种表观遗传标记可能有助于早期识别患有OWO风险的儿童.
科学领域:
- 健康和疾病的表观遗传学和发育起源 (DOHaD)
- 儿科内分泌学和肥胖研究
- 在生命早期发现生物标志物
背景情况:
- 通过新生儿DNA甲基化 (GAmAge) 估计的妊娠年龄与产前暴露和直接出生结果相关.
- GAmAge与长期超重或肥胖 (OWO) 轨迹之间的关联仍在调查中.
研究的目的:
- 确定GAmAge是否与从出生到18岁的长期体重指数百分位数 (BMIPCT) 轨迹有关.
- 探索GAmAge作为预测OWO发展的潜在早期生物标志物.
主要方法:
- 从带血DNA甲基化概况计算的GAmAge来自美国出生队列的831名儿童.
- 使用重复的人类测量测量,定义了长期体重轨迹 (出生至18岁).
- 分析了GAmAge和BMIPCT轨迹之间的关联,并对共变量进行调整.
主要成果:
- GAmAge区分稳定的正常重量轨迹和不稳定的轨迹与晚期或非常晚期OWO发展.
- 关联从出生到14岁是显著的,并且在调整妊娠年龄,母亲吸烟,分娩方式和孩子的性别后仍然存在.
- 出生体重调解了GAmAge对特定群体和年龄段OWO状态的影响.
结论:
- GAmAge与从出生到18岁的BMIPCT轨迹有关,独立于妊娠年龄和出生体重.
- GAmAge显示出作为预测BMI轨迹的早期生物标志物的潜力,并为OWO风险评估和预防策略提供信息.
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