Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, China.
NTU Psychology, Nottingham Trent University, Nottingham, United Kingdom.
Front Public Health. 2024 Sep 30;12:1377070. doi: 10.3389/fpubh.2024.1377070. eCollection 2024.
Prenatal drug use may cause toxicity to bone health in newborns. We aimed to examine whether birth outcomes mediate the association between medication use and neonatal metabolic bone disease (MBD).
A prospective cohort of 10,801 pregnant women (17-49 years) and their infants followed at a single center from 1 January 2012 to 31 December 2021 were included. Based on four single drugs, comprehensive medication use was determined and categorized into three groups using latent-class analysis: group 1 included antibiotics and furosemide or less than two drugs except for MgSO; group 2 included MgSO without antibiotics or furosemide; and group 3 encompassed dexamethasone and antibiotics. Mediation analysis was conducted to assess the mediating effects of prematurity, low birth weight (LBW), and small for gestational age (SGA).
There were 138 (1.3%) infants with MBD; 2,701 (25%) were born preterm, 1717 (15.9%) had LBW, and 303 (2.8%) were SGA. Pregnant women in groups 2 and 3 were 2.52 to 14.66 times more likely to deliver an infant with MBD than those in group 1. Only LBW showed a significant mediating effect on the association between comprehensive medication use and MBD, with a mediation proportion of 51.8% (45.0-64.1%, < 0.001).
Comprehensive medication use during pregnancy was associated with an increased risk of neonatal MBD, largely mediated by LBW. Early antepartum monitoring and prevention targeting adverse birth outcomes are necessary to mitigate the risk of MBD.
产前药物使用可能导致新生儿骨骼健康毒性。我们旨在研究药物使用与新生儿代谢性骨病(MBD)之间的关联是否由出生结局介导。
本研究纳入了 2012 年 1 月 1 日至 2021 年 12 月 31 日期间在单中心接受随访的 10801 名孕妇(17-49 岁)及其婴儿的前瞻性队列。基于四种单一药物,通过潜在类别分析确定了综合用药情况,并分为三组:组 1 包括抗生素和呋塞米或少于两种药物,不包括 MgSO;组 2 包括无抗生素和呋塞米的 MgSO;组 3 包括地塞米松和抗生素。进行中介分析以评估早产、低出生体重(LBW)和小于胎龄儿(SGA)的中介作用。
有 138 名(1.3%)婴儿患有 MBD;2701 名(25%)早产儿、1717 名(15.9%)LBW 和 303 名(2.8%)SGA。组 2 和组 3 的孕妇分娩患有 MBD 的婴儿的可能性是组 1 的 2.52 至 14.66 倍。只有 LBW 对综合用药与 MBD 之间的关联具有显著的中介作用,中介比例为 51.8%(45.0-64.1%, <0.001)。
孕妇在怀孕期间的综合用药与新生儿 MBD 的风险增加有关,主要由 LBW 介导。早期产前监测和针对不良出生结局的预防措施对于降低 MBD 的风险是必要的。