儿童时期患脑膜炎后出现精神神经发育障碍的风险:一项基于全国人口的队列研究。

Infectious diseases (London, England) Pub Date : 2025-01-01 Epub Date: 2024-09-04 DOI:10.1080/23744235.2024.2399101
Emma E Graham, Malte M Tetens, Jacob Bodilsen, Ram Dessau, Svend Ellermann-Eriksen, Nanna S Andersen, Charlotte Sværke Jørgensen, Michael Pedersen, Kirstine K Søgaard, Jette Bangsborg, Alex Christian Nielsen, Jens Kjølseth Møller, Dorrit Obel, Anne-Mette Lebech, Ulrikka Nygaard, Lars H Omland, Niels Obel
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引用次数: 0

摘要

背景:很少有研究调查了儿童脑膜炎后出现精神神经发育障碍(PNDD)的风险:很少有研究调查儿童脑膜炎后患精神神经发育障碍(PNDD)的风险:全国性人群队列研究(丹麦,1995-2021 年),研究对象为脑脊液细菌或肠道病毒检测呈阳性的儿童,按年龄分为幼儿(0 至 n = 637)或较大儿童(≥90 天至 n = 1,218)。我们从普通人群(n = 18,550)中建立了一个对比队列,并建立了参与者的兄弟姐妹队列。作为PNDD的风险估计值,我们计算了经年龄和性别调整的危险比(aHRs)及95%置信区间(95%CI):结果:细菌性脑膜炎患儿罹患 PNDD 的风险增加,尤其是学习和智力发育障碍(幼儿:aHR 4.2,95%CI:2.4-7.1;大龄儿童:aHR 1.5,95%CI:1.0-2.3)、注意力缺陷障碍(AD)和发育障碍(PNDD)。3)、注意力缺陷障碍(ADHD)(幼儿:aHR 2.8,95%CI:1.5-5.2;大龄儿童:1.4,95%CI:0.9-2.2)和放弃 ADHD 药物治疗(幼儿:aHR 2.2,95%CI:1.0-4.7;大龄儿童:1.5,95%CI:1.0-2.3)。此外,患有细菌性脑膜炎的幼儿患自闭症谱系障碍(aHR 1.9,95%CI:0.9-4.1)以及行为和情绪障碍(aHR 2.0,95%CI:1.0-3.9)的风险也有所增加。在婴幼儿中,早产儿患 PNDD 的风险尤其高。患有细菌性脑膜炎的大龄儿童的兄弟姐妹患 PNDD 的风险也会增加。在任何年龄段患有肠道病毒脑膜炎的儿童,其罹患PNDD或放弃ADHD药物治疗的风险都没有增加:结论:儿童时期的细菌性脑膜炎与随后的 PNDD 诊断有关,而肠道病毒性脑膜炎与之无关。这种关联的部分原因似乎是早产以及家庭和社会经济因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of psychiatric neurodevelopmental disorders after meningitis in childhood: a nationwide, population-based cohort study.

Background: Few studies have investigated the risk of psychiatric neurodevelopmental disorders (PNDD) after childhood meningitis.

Methods: Nationwide population-based cohort study (Denmark, 1995-2021) of children with positive cerebrospinal fluid for bacteria or enterovirus, stratified on age as young infants (0 to <90 days, n = 637) or older children (≥90 days to <17 years, n = 1,218). We constructed a comparison cohort from the general population (n = 18,550), and cohorts of siblings of participants. As risk estimates of PNDD we calculated age- and sex-adjusted hazard ratios (aHRs) with 95% confidence intervals (95%CI).

Results: Children with bacterial meningitis had increased risks of PNDD, especially learning and intellectual developmental disorders (young infants: aHR 4.2, 95%CI: 2.4-7.1; older children: aHR 1.5, 95%CI: 1.0-2.3), attention deficit disorder (ADHD) (young infants: aHR 2.8, 95%CI: 1.5-5.2; older children: 1.4, 95%CI: 0.9-2.2) and redemption of ADHD medication (young infants: aHR 2.2, 95%CI: 1.0-4.7; older children: 1.5, 95%CI: 1.0-2.3). Young infants with bacterial meningitis additionally had increased risks of autism spectrum disorders (aHR 1.9, 95%CI: 0.9-4.1) and behavioural and emotional disorders (aHR 2.0, 95%CI: 1.0-3.9). In young infants, the excess risk of PNDD was especially observed in premature children. Siblings of older children with bacterial meningitis also had increased risks of PNDD. Children with enteroviral meningitis at any age did not have increased risks of PNDD or redemption of ADHD medication.

Conclusions: Bacterial meningitis in childhood is associated with subsequent diagnosis of PNDD, while enteroviral meningitis is not. The association appears to be partly explained by prematurity and familial and socioeconomic factors.

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