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患有先天性腹壁缺陷的儿童的神经发育障碍:一项基于全国人口的研究
Anna Fogelström1,2, Charlotte Skoglund3, Eva Hagel4
1Division of Pediatric Surgery, Astrid Lindgren Children's Hospital, C11:33, Karolinska University Hospital, 17176, Stockholm, Sweden. anna.fogelstrom@ki.se.
Pediatric surgery international
|September 22, 2025
概括
出生时患有腹壁缺陷 (AWD) 的儿童患有自闭症谱系障碍 (ASD) 的风险更高,特别是患有腹的儿童. 然而,注意力缺陷/多动障碍 (ADHD) 的风险与同龄人相似.
科学领域:
- 儿科手术 儿科手术
- 发育儿科 发育儿科
- 公共卫生 公共卫生
背景情况:
- 腹壁缺陷 (AWD),包括腹和胃,影响大约每4000名瑞典新生儿中的1名.
- 患有AWD儿童的长期神经发育结果和发病率尚未得到充分了解.
研究的目的:
- 为了调查神经发育障碍的风险,特别是自闭症谱系障碍 (ASD) 和注意力缺陷/多动症障碍 (ADHD),在出生时患有脑或胃的儿童中.
主要方法:
- 瑞典 (1997-2016) 基于人口的国家队列研究.
- 包括患有腹或胃的儿童,不包括染色体异常的儿童.
- 在每个AWD病例中匹配了10个未暴露的个体.
- 利用国家卫生登记处收集关于ASD和ADHD诊断的数据.
主要成果:
- 与未暴露的同龄人相比 (p=0.02) 的OMPHALOCELE队列显示出明显更高的ASD风险 (HR=3.51).
- 在AWD队列和未暴露的对照组之间没有观察到ADHD发病率的显著差异.
- 尽管特定子组的风险增加,神经发育障碍的总体发病率仍然相对较低.
结论:
- 患有AWD的儿童通常具有与同龄人相似的ADHD风险.
- 奥姆法洛塞尔与ASD的发病率增加有关,尽管整体发病率较低.
- 对AWD患者长期神经发育轨迹的进一步研究是有必要的.
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