有或没有产前物质暴露的青少年的不良童年经历和神经发育障碍:一项纵向匹配的基于登记的队列研究。

IF 1.9 3区 社会学 Q3 SUBSTANCE ABUSE Nordic Studies on Alcohol and Drugs Pub Date : 2023-04-01 DOI:10.1177/14550725221110190
Anne M Koponen, Niina-Maria Nissinen, Mika Gissler, Ilona Autti-Rämö, Hanna Kahila, Taisto Sarkola
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摘要

背景:先前的研究表明,不良童年经历(ace)与产前物质暴露(PSE)青少年继发精神健康问题之间存在关联,但ace与神经发育障碍之间的关联尚不清楚。方法:这项基于纵向登记的队列研究调查了PSE青少年(酒精/药物,n = 615)和匹配的未暴露对照组(n = 1787)中出生时健康状况、ace(户外护理(OHC)和母亲逆境)和神经发育障碍之间的关系。合并医院病历和登记数据,并使用Cox回归模型进行分析。结果:行为和情绪障碍(国际疾病及相关健康问题统计分类ICD-10, F90-F94)在暴露者中比对照组更常见,但只有在暴露者和没有OHC的对照组进行比较时才如此。在多动障碍(ADHD, F90)、行为和情绪混合障碍(F92)和儿童期特异性情绪障碍(F93)中出现了差异。在OHC暴露者和对照组中,超过40%的人被诊断为F90-F94。对于特定的发育障碍(F80-F83,例如,言语和语言障碍以及学习技能),在调整OHC后,暴露者和对照组之间的中度差异减弱。同样,暴露于热含量暴露的人群和热含量暴露的对照组的发病率最高。OHC和产妇风险是相互关联的,并且与男性和低出生体重一起,在暴露者和对照组中都与神经发育障碍有关,并缩小了它们之间的差异。结论:ace与神经发育障碍之间存在很强的相关性。需要进行脑研究来检验ace是否会恶化PSE引起的神经发育结果。
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Adverse childhood experiences and neurodevelopmental disorders among youth with and without prenatal substance exposure: A longitudinal matched register-based cohort study.

Background: Previous research has shown an association between adverse childhood experiences (ACEs) and secondary mental health problems in youth with prenatal substance exposure (PSE), but the association between ACEs and neurodevelopmental disorders is less clear. Methods: This longitudinal register-based cohort study investigated relationships between health at birth, ACEs (out-of-home care (OHC) and maternal adversities), and neurodevelopmental disorders among youth with PSE (alcohol/drugs, n = 615) and matched unexposed controls (n = 1787). Hospital medical records and register data were merged and analysed using Cox regression models. Results: Conduct and emotional disorders (International Statistical Classification of Diseases and Related Health Problems ICD-10, F90-F94) were more common among the exposed than the controls but only when the exposed and controls with no OHC were compared. The difference appeared in hyperkinetic disorders (ADHD, F90), mixed disorders of conduct and emotions (F92) and emotional disorders with onset specific to childhood (F93). Among the exposed and controls with OHC, over 40% had received an F90-F94 diagnosis. Regarding specific developmental disorders (F80-F83, e.g., impairments in speech and language and scholastic skills) the moderate difference between the exposed and controls attenuated after adjustment for OHC. Again, the rates were highest among the exposed with OHC and the controls with OHC. OHC and maternal risks were interrelated and, together with male sex and low birth weight, were associated with neurodevelopmental disorders both among the exposed and controls and decreased the difference between them. Conclusions: A strong association between ACEs and neurodevelopmental disorders was found. Brain research is needed to examine whether ACEs worsen neurodevelopmental outcomes caused by PSE.

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来源期刊
CiteScore
3.90
自引率
11.80%
发文量
36
审稿时长
30 weeks
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