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产前皮质类固醇治疗对动物模型的长期神经病理学和/或神经行为学影响:系统评价。

Long-term neuropathological and/or neurobehavioral effects of antenatal corticosteroid therapy in animal models: a systematic review.

机构信息

Department of Development and Regeneration, Cluster Woman and Child, Faculty of Medicine, KU Leuven, Leuven, Belgium.

Department of Obstetrics and Gynaecology, Fetal Medicine Unit, UZ Leuven, Leuven, Belgium.

出版信息

Pediatr Res. 2020 Jun;87(7):1157-1170. doi: 10.1038/s41390-019-0712-1. Epub 2019 Dec 10.

Abstract

BACKGROUND

Antenatal corticosteroids (ACSs) are recommended to all women at risk for preterm delivery; currently, there is controversy about the subsequent long-term neurocognitive sequelae. This systematic review summarizes the long-term neurodevelopmental outcomes after ACS therapy in animal models.

METHODS

An electronic search strategy incorporating MeSH and keywords was performed using all known literature databases and in accordance with PRISMA guidance (PROSPERO CRD42019119663).

RESULTS

Of the 669 studies identified, eventually 64 were included. The majority of studies utilized dexamethasone at relative high dosages and primarily involved rodents. There was a high risk of bias, mostly due to lack of randomization, allocation concealment, and blinding. The main outcomes reported on was neuropathological, particularly glucocorticoid receptor expression and neuron densities, and neurobehavior. Overall there was an upregulation of glucocorticoid receptors with lower neuron densities and a dysregulation of the dopaminergic and serotonergic systems. This coincided with various adverse neurobehavioral outcomes.

CONCLUSIONS

In animal models, ACSs consistently lead to deleterious long-term neurocognitive effects. This may be due to the specific agents, i.e., dexamethasone, or the repetitive/higher total dosing used. ACS administration varied significantly between studies and there was a high risk of bias. Future research should be standardized in well-characterized models.

摘要

背景

产前皮质类固醇(ACS)被推荐用于所有有早产风险的女性;目前,对于 ACS 治疗后的后续长期神经认知后遗症存在争议。本系统评价总结了 ACS 治疗后动物模型的长期神经发育结局。

方法

采用电子检索策略,结合 MeSH 和关键词,使用所有已知的文献数据库,并按照 PRISMA 指南(PROSPERO CRD42019119663)进行检索。

结果

在 669 项研究中,最终有 64 项被纳入。大多数研究使用相对较高剂量的地塞米松,主要涉及啮齿动物。存在很高的偏倚风险,主要是由于缺乏随机分组、分配隐匿和盲法。主要报告的结果是神经病理学,特别是糖皮质激素受体表达和神经元密度以及神经行为。总的来说,糖皮质激素受体的上调与神经元密度的降低以及多巴胺能和 5-羟色胺能系统的失调有关。这与各种不良的神经行为结果一致。

结论

在动物模型中,ACS 始终导致有害的长期神经认知影响。这可能是由于特定的药物,即地塞米松,或使用的重复/更高的总剂量。ACS 的给药在研究之间存在显著差异,且存在很高的偏倚风险。未来的研究应在经过良好特征描述的模型中标准化。

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