A serial analysis of serum aspartate aminotransferase levels in patients with acute encephalopathy with biphasic seizures and late reduced diffusion and prolonged febrile seizure

IF 1.4 4区 医学 Q4 CLINICAL NEUROLOGY
Ayaka Kasai , Mitsuo Motobayashi , Makoto Nishioka , Tetsuhiro Fukuyama , Yuji Inaba
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引用次数: 0

Abstract

Background

There are no established biomarkers for diagnosing acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) in the early acute phase, called “the 1st seizure phase”. Based on our clinical experience, we hypothesized that serial examinations of blood levels of aspartate aminotransferase (AST) in children with febrile convulsive status epilepticus (FCSE) revealed higher levels in patients with AESD in the 1st seizure phase than in those with prolonged febrile seizures (PFs).

Methods

To test our presented hypothesis, we retrospectively investigated changes in serum AST in patients with FCSE due to AESD (n = 11) or PFs (n = 27) who were serially examined within 48 h of the onset of convulsions.

Results

The rate of increase in AST was significantly higher in patients with AESD than in those with PFs. The rate of increase in AST correlated with previously reported scoring systems, i.e., Yokochi and Tottori scores, for the prediction of AESD. A positive correlation between the rate of increase in AST and creatinine levels in the first examination were observed; however, creatinine levels did not significantly differ between the AESD and PFs groups in the first or second examination. Blood levels of pH, ammonia, and sugar in the first examination and C-reactive protein in the second examination were significantly higher in the AESD group than in the PFs group.

Conclusions

The present study revealed that the rate of increase in AST was significantly higher in patients with AESD than in those with PFs. A novel predictive scoring system needs to be established in combination with the rate of increase in AST and reported clinical parameters, which will improve the prognosis of patients with FCSE.

急性脑病伴双相发作、迟发性扩散减少和高热惊厥患者血清天冬氨酸转氨酶水平的系列分析
背景:目前还没有确定的生物标志物来诊断急性脑病,包括急性早期的双相癫痫发作和晚期扩散减少(AESD),称为“第一发作期”。根据我们的临床经验,我们假设对患有热性惊厥性癫痫持续状态(FCSE)的儿童的天冬氨酸转氨酶(AST)水平进行一系列检查,结果显示,在第一次癫痫发作期的AESD患者的AST水平高于长期热性癫痫发作(PFs)的患者,我们回顾性研究了因AESD(n=11)或PFs(n=27)引起的FCSE患者的血清AST变化,这些患者在抽搐发作后48小时内进行了连续检查。结果AESD患者AST升高率明显高于PFs患者。AST的增长率与先前报道的评分系统相关,即预测AESD的Yokochi和Tottori评分。在第一次检查中,AST的增加率与肌酐水平呈正相关;然而,在第一次或第二次检查中,AESD组和PFs组之间的肌酸酐水平没有显著差异。AESD组第一次检查的血液pH、氨和糖水平以及第二次检查的C反应蛋白水平显著高于PFs组。结论本研究显示,AESD患者AST的增加率明显高于PFs患者。需要结合AST的增加率和报告的临床参数建立一种新的预测性评分系统,以改善FCSE患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Brain & Development
Brain & Development 医学-临床神经学
CiteScore
3.60
自引率
0.00%
发文量
153
审稿时长
50 days
期刊介绍: Brain and Development (ISSN 0387-7604) is the Official Journal of the Japanese Society of Child Neurology, and is aimed to promote clinical child neurology and developmental neuroscience. The journal is devoted to publishing Review Articles, Full Length Original Papers, Case Reports and Letters to the Editor in the field of Child Neurology and related sciences. Proceedings of meetings, and professional announcements will be published at the Editor''s discretion. Letters concerning articles published in Brain and Development and other relevant issues are also welcome.
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