The Department of Pediatrics, Northwestern University, Chicago, Illinois, USA.
The George Washington University Biostatistics Center, Washington, District of Columbia, USA.
Dev Neurosci. 2022;44(4-5):412-425. doi: 10.1159/000525483. Epub 2022 Jun 15.
The Beneficial Effects of Antenatal Magnesium clinical trial was conducted between 1997 and 2007, and demonstrated a significant reduction in cerebral palsy (CP) in preterm infants who were exposed to peripartum magnesium sulfate (MgSO4). However, the mechanism by which MgSO4 confers neuroprotection remains incompletely understood. Cord blood samples from this study were interrogated during an era when next-generation sequencing was not widely accessible and few gene expression differences or biomarkers were identified between treatment groups. Our goal was to use bulk RNA deep sequencing to identify differentially expressed genes comparing the following four groups: newborns who ultimately developed CP treated with MgSO4 or placebo, and controls (newborns who ultimately did not develop CP) treated with MgSO4 or placebo. Those who died after birth were excluded. We found that MgSO4 upregulated expression of SCN5A only in the control group, with no change in gene expression in cord blood of newborns who ultimately developed CP. Regardless of MgSO4 exposure, expression of NPBWR1 and FTO was upregulated in cord blood of newborns who ultimately developed CP compared with controls. These data support that MgSO4 may not exert its neuroprotective effect through changes in gene expression. Moreover, NPBWR1 and FTO may be useful as biomarkers and may suggest new mechanistic pathways to pursue in understanding the pathogenesis of CP. The small number of cases ultimately available for this secondary analysis, with male predominance and mild CP phenotype, is a limitation of the study. In addition, differentially expressed genes were not validated by qRT-PCR.
产前镁临床试验于 1997 年至 2007 年进行,结果表明,接受围产期硫酸镁(MgSO4)治疗的早产儿脑瘫(CP)显著减少。然而,MgSO4 发挥神经保护作用的机制仍不完全清楚。本研究的脐带血样本是在下一代测序尚未广泛应用且治疗组之间很少有基因表达差异或生物标志物被鉴定的时代进行检测的。我们的目标是使用批量 RNA 深度测序来识别以下四个组之间的差异表达基因:最终接受 MgSO4 或安慰剂治疗的脑瘫新生儿,以及最终未发展为 CP 的接受 MgSO4 或安慰剂治疗的对照组新生儿。排除出生后死亡的新生儿。我们发现,MgSO4 仅在对照组中上调 SCN5A 的表达,而在最终发展为 CP 的新生儿脐带血中基因表达没有变化。无论是否暴露于 MgSO4,最终发展为 CP 的新生儿的脐带血中 NPBWR1 和 FTO 的表达均上调,而对照组则无此现象。这些数据表明,MgSO4 可能不会通过改变基因表达来发挥其神经保护作用。此外,NPBWR1 和 FTO 可能是有用的生物标志物,并且可能提示我们可以通过探索理解 CP 发病机制的新机制途径来探索它们。本二次分析最终可用的病例数量较少,且以男性为主,CP 表型较轻,这是该研究的局限性。此外,差异表达基因未通过 qRT-PCR 进行验证。