Laugesen Kristina, Skajaa Nils, Petersen Irene, Skovsager Andersen Marianne, Feldt-Rasmussen Ulla, Kejlberg Al-Mashhadi Sofie, Stewart Paul, Lunde Jørgensen Jens Otto, Toft Sørensen Henrik
Department of Clinical Epidemiology, Department of Clinical Medicine, Aarhus University Hospital, Aarhus University, Aarhus, Denmark.
Department of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark.
JAMA Netw Open. 2025 Jan 2;8(1):e2453245. doi: 10.1001/jamanetworkopen.2024.53245.
Current evidence of the association between prenatal exposure to glucocorticoids and long-term mental disorders is scarce and has limitations.
To investigate the association between prenatal exposure to systemic glucocorticoids and mental disorders in offspring at the age of 15 years, comparing exposed vs unexposed offspring born to mothers with the same underlying disease (risk of preterm delivery and autoimmune or inflammatory disorders).
DESIGN, SETTING, AND PARTICIPANTS: This nationwide population-based cohort study used data from registries in Denmark with follow-up until December 31, 2018. Participants included all Danish infants born alive from 1996 to 2016. Analyses were performed from January to December 2023.
Prenatal exposure to systemic glucocorticoids.
Fifteen-year crude and adjusted risks, risk differences, and risk ratios (RR) for mental disorders using Kaplan-Meier estimator comparing exposed vs unexposed offspring born to mothers with the same underlying disease.
A total of 1 061 548 infants (52% male) were included in the final study cohort, including 31 518 born to mothers at risk of preterm delivery and 288 747 born to mothers with autoimmune or inflammatory disorders. Among offspring born to mothers at risk of preterm delivery, the adjusted risks for exposed vs unexposed were 6.6% vs 4.3% (RR, 1.5 [95% CI, 1.2-1.9]) for autism spectrum disorders; 1.6% vs 1.3% (RR, 1.3 [95% CI, 0.8-1.8]) for intellectual disabilities; 5.8% vs 4.3% (RR, 1.3 [95% CI, 1.0-1.7]) for attention-deficit hyperactivity disorder (ADHD); and 7.2% vs 4.6% (RR, 1.5 [95% CI, 1.1-2.0]) for mood, anxiety, and stress-related disorders. Among offspring born to mothers with autoimmune or inflammatory disorders, the adjusted risks for exposed vs unexposed were 4.8% vs 3.8% (RR, 1.3 [95% CI, 1.1-1.5]) for autism spectrum disorders; 1.1% vs 0.8% (RR 1.4, [95% CI, 0.9-2.0]) for intellectual disabilities; 5.5% vs 4.4% (RR, 1.3 [95% CI, 1.0-1.5]) for ADHD; and 6.6% vs 4.6% (RR, 1.4 [95% CI, 1.2-1.8]) for mood, anxiety, and stress-related disorders. Findings were confirmed through an active comparator and sibling design. However, confounding by disease severity could not be ruled out.
In this cohort study, prenatal exposure to glucocorticoids was associated with higher risk of some mental disorders. These data support continued caution in the use of glucocorticoids in pregnant people.
目前关于产前接触糖皮质激素与长期精神障碍之间关联的证据稀少且存在局限性。
调查产前全身性接触糖皮质激素与15岁后代精神障碍之间的关联,比较患有相同基础疾病(早产风险以及自身免疫性或炎症性疾病)的母亲所生的暴露组与未暴露组后代。
设计、背景和参与者:这项基于全国人群的队列研究使用了丹麦登记处的数据,随访至2018年12月31日。参与者包括1996年至2016年所有丹麦活产婴儿。分析于2023年1月至12月进行。
产前全身性接触糖皮质激素。
使用Kaplan-Meier估计量比较患有相同基础疾病的母亲所生的暴露组与未暴露组后代,得出15岁时精神障碍的粗风险和调整风险、风险差异及风险比(RR)。
最终研究队列共纳入1061548名婴儿(52%为男性),其中31518名母亲有早产风险所生的婴儿,以及288747名母亲患有自身免疫性或炎症性疾病所生的婴儿。在有早产风险的母亲所生的后代中,暴露组与未暴露组相比自闭症谱系障碍的调整风险分别为6.6%和4.3%(RR,1.5[95%CI,1.2 - 1.9]);智力残疾分别为1.6%和1.3%(RR,1.3[95%CI,0.8 - 1.8]);注意力缺陷多动障碍(ADHD)分别为5.8%和4.3%(RR,1.3[95%CI,1.0 - 1.7]);情绪、焦虑和压力相关障碍分别为7.2%和4.6%(RR,1.5[95%CI,1.1 - 2.0])。在患有自身免疫性或炎症性疾病的母亲所生的后代中,暴露组与未暴露组相比自闭症谱系障碍的调整风险分别为4.8%和3.8%(RR,1.3[95%CI,1.1 - 1.5]);智力残疾分别为1.1%和0.8%(RR 1.4,[95%CI,0.9 - 2.0]);ADHD分别为5.5%和4.4%(RR,1.3[95%CI,1.0 - 1.5]);情绪、焦虑和压力相关障碍分别为6.6%和4.6%(RR,1.4[95%CI,1.2 - 1.8])。研究结果通过主动对照和同胞设计得到了证实。然而,疾病严重程度的混杂因素无法排除。
在这项队列研究中,产前接触糖皮质激素与某些精神障碍的较高风险相关。这些数据支持在孕妇中使用糖皮质激素时应持续谨慎。