全表观基因组关联研究确定了新生儿DNA甲基化与非常早产儿童的两年注意力问题相关
Marie Camerota1,2, Barry M Lester3,4,5, Francisco Xavier Castellanos6,7
1Department of Psychiatry and Human Behavior, Alpert Medical School of Brown University, Providence, RI, USA. marie_camerota@brown.edu.
Translational psychiatry
|February 28, 2024
概括
新生儿DNA甲基化预测到两岁时,非常早产的婴儿会出现注意力问题. 这些表观遗传信息可能有助于识别有风险的儿童,以便进行早期干预.
科学领域:
- 神经科学是一个神经科学.
- 遗传学 遗传学 是一个
- 发展心理学 发展心理学
背景情况:
- 之前的研究已经确定了年龄较大的儿童注意力问题的表观遗传预测因素.
- 这些预测因素尚未在幼儿或因早产而面临高风险的儿童中进行研究.
研究的目的:
- 为了研究新生儿DNA甲基化和两岁时非常早产婴儿的注意力问题之间的全表观基因组相关性.
- 为了确定潜在的早期生物标志物注意力困难在这个脆弱的人群.
主要方法:
- 该研究分析了441名非常早产婴儿 (<30周妊娠年龄) 的新生儿神经行为和非常早产婴儿结果研究 (NOVI) 的数据.
- 新生儿DNA甲基化被测量使用口腔拭子和Illumina甲基化EPIC珠子阵列.
- 两年后,使用儿童行为检查表 (CBCL) 评估了注意力问题.
主要成果:
- 在调整为多次测试后,33个CpG位点的DNA甲基化显著与注意力问题有关.
- 这些CpG位点位于以前与ADHD和其他健康状况相关的基因中.
- 在NOVI样本中,一些地点也与产前风险因素有关.
结论:
- 新生儿表观遗传学在NICU出院时进行评估,可以帮助识别患注意力障碍风险的早产婴儿.
- 早期发现可能有助于及时预防和干预注意力缺陷和相关精神疾病.
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