Factors influencing efficacy and relapse of adrenocorticotropic hormone in infantile epileptic spasms syndrome

IF 2.3 3区 医学 Q2 BEHAVIORAL SCIENCES Epilepsy & Behavior Pub Date : 2024-09-22 DOI:10.1016/j.yebeh.2024.110055
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Abstract

Background

Infantile epileptic spasms syndrome (IESS) is a severe epileptic condition characterized by persistent uncontrolled seizures, with some children experiencing recurrent seizures despite multiple pharmacological therapies. The prognostic risk factors associated with IESS remain unclear. This study aimed to evaluate the factors influencing the efficacy and relapse of adrenocorticotropic hormone (ACTH) treatment for IESS in infants, as well as to assess the correlation between the Burden of Amplitudes and Epileptiform Discharges (BASED) score and clinical outcomes.

Methods

A retrospective analysis was conducted on a cohort of 88 pediatric patients diagnosed with IESS who received ACTH therapy at our hospital from February 2016 to August 2023. Patients were categorized into response (n = 47) and non-response (n = 41) groups based on their treatment response at day 28. Responders were further classified into relapse and non-relapse groups. A modified Poisson regression model and receiver operating characteristic (ROC) curves were employed to evaluate the positive predictive values.

Results

In this study, a total of 47 patients (53.4 %) responded to ACTH treatment. Patients in the response group demonstrated significantly greater reductions in BASED scores by day 14 of ACTH treatment, yielding an area under the curve (AUC) of 0.859 (95 % CI: 0.782–0.937, P<0.05), with a sensitivity of 68.1 % and a specificity of 95.1 %. The optimal cut-off point was established at ≥ 2, corresponding to a Youden index of 0.632. Notably, patients who were on anti-seizure medications (ASMs) before ACTH treatment and those with developmental delay prior to the onset of spasms exhibited lower short-term response rates (P<0.05), although these factors did not demonstrate predictive value. Among the responders, 20 cases (42.6 %) experienced a relapse, with only those patients showing specific abnormalities on cranial magnetic resonance imaging (MRI) exhibiting a statistically higher proportion of relapse.

Conclusion

Patients receiving ASMs before ACTH treatment and those with developmental delays prior to the onset of spasms may have a less favorable therapeutic response. A reduction in BASED scores of 2 or greater by day 14 of ACTH treatment may signify a potentially positive treatment response. Additionally, patients with IESS who present with specific abnormalities on cranial MRI may have an increased likelihood of relapse following ACTH treatment.
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影响婴儿癫痫痉挛综合征肾上腺皮质激素疗效和复发的因素。
背景:婴儿癫痫性痉挛综合征(IESS)是一种严重的癫痫疾病,其特点是癫痫发作持续不受控制,有些患儿在接受多种药物治疗后仍会反复发作。与IESS相关的预后风险因素仍不清楚。本研究旨在评估婴儿促肾上腺皮质激素(ACTH)治疗 IESS 的疗效和复发的影响因素,以及评估癫痫样放电和振幅负担(BASED)评分与临床结果之间的相关性:我们对2016年2月至2023年8月期间在本院接受ACTH治疗的88名确诊为IESS的儿科患者进行了回顾性分析。根据第28天的治疗反应,将患者分为有反应组(n = 47)和无反应组(n = 41)。有反应者又分为复发组和非复发组。采用改良泊松回归模型和接收器操作特征曲线来评估阳性预测值:在这项研究中,共有 47 名患者(53.4%)对促肾上腺皮质激素治疗产生了反应。在 ACTH 治疗的第 14 天,应答组患者的 BASED 评分明显降低,曲线下面积(AUC)为 0.859(95 % CI:0.782-0.937,P<0.05),灵敏度为 68.1%,特异性为 95.1%。最佳临界点确定为≥2,即尤登指数为 0.632。值得注意的是,在接受促肾上腺皮质激素治疗前服用抗癫痫药物(ASMs)的患者和在痉挛发生前发育迟缓的患者的短期反应率较低(P<0.05),尽管这些因素并未显示出预测价值。在有反应的患者中,有20例(42.6%)复发,只有那些在头颅磁共振成像(MRI)上显示出特殊异常的患者的复发比例在统计学上更高:结论:在接受促肾上腺皮质激素治疗前接受ASMs治疗的患者,以及在痉挛发生前有发育迟缓的患者,其治疗反应可能较差。如果在接受 ACTH 治疗的第 14 天,BASED 评分降低 2 分或更多,则可能意味着治疗反应良好。此外,头颅核磁共振成像(MRI)出现特殊异常的 IESS 患者在接受 ACTH 治疗后复发的可能性可能会增加。
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
Epilepsy & Behavior
Epilepsy & Behavior 医学-行为科学
CiteScore
5.40
自引率
15.40%
发文量
385
审稿时长
43 days
期刊介绍: Epilepsy & Behavior is the fastest-growing international journal uniquely devoted to the rapid dissemination of the most current information available on the behavioral aspects of seizures and epilepsy. Epilepsy & Behavior presents original peer-reviewed articles based on laboratory and clinical research. Topics are drawn from a variety of fields, including clinical neurology, neurosurgery, neuropsychiatry, neuropsychology, neurophysiology, neuropharmacology, and neuroimaging. From September 2012 Epilepsy & Behavior stopped accepting Case Reports for publication in the journal. From this date authors who submit to Epilepsy & Behavior will be offered a transfer or asked to resubmit their Case Reports to its new sister journal, Epilepsy & Behavior Case Reports.
期刊最新文献
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