Boronat Susana, Turon-Viñas Eulalia, Mac Manus Noel, Diaz-Gomez Asuncion, Vicente Mónica, Ros-Castelló Victoria, Sierra-Marcos Alba
Pediatric Neurology Unit, Hospital de la Santa Creu i Sant Pau, Barcelona, UAB, Barcelona, Spain.
Neurophysiology Unit. Vall d'Hebron Hospital. Barcelona, UAB, Barcelona, Spain.
Epilepsia Open. 2024 Dec;9(6):2505-2509. doi: 10.1002/epi4.13077. Epub 2024 Nov 6.
Type I Alexander disease (AxD) presents with paroxysmal neurodegeneration, refractory epilepsy, and encephalopathy in the first years of life and is associated with a poor prognosis. Although there is no treatment, mild symptomatic improvement has been reported in one case of adult Alexander treated with ceftriaxone, given its interaction with the mutant glial fibrillary acid protein (GFAP) responsible for the disease's pathogenesis. We describe a patient presenting with irritability starting at 2 months of age, initially attributed to gastroesophageal reflux. A ventriculoperitoneal shunt was placed at 3 months of age due to hydrocephalus secondary to aqueduct stenosis detected through an MRI scan, but the irritability persisted. At 5 months, a new brain MRI was performed due to irritability worsening, onset of abnormal ocular movements and seizures. In addition genetic testing was performed. AxD was diagnosed due to the mutation c.716G>A (p.Arg239His) in GFAP. Since irritability had worsened and had not responded to levomepromazine, treatment with amoxicillin (80 mg/kg/day) was attempted to modulate glutamate levels. The patient showed a striking improvement of irritability in 48 h that persisted over the next months. The patient had frequent daily seizures which did not respond to valproate, clonazepam, or phenobarbital. Perampanel, a postsynaptic AMPA receptor antagonist, was added to phenobarbital and he was seizure free for more than 3 months. Drugs modulating glutamate levels in the central nervous system, including β-lactam antibiotics and perampanel, may have an important role in the symptomatic treatment of AxD and other neurodegenerative diseases where glutamatergic excitotoxicity is a pathogenic determinant. PLAIN LANGUAGE SUMMARY: Alexander disease is a rare and serious condition that affects the brain, often leading to neurodegeneration (brain damage), seizures, and other problems in early childhood. The disease is caused by a mutation in a gene called GFAP. There is no cure, and current treatments mainly focus on relieving symptoms. This article discusses the case of a baby who showed signs of irritability and seizures from a young age. The baby was diagnosed with Alexander disease after brain scans and genetic testing. Despite treatment with various drugs, the baby continued to experience seizures and irritability. The doctors decided to try amoxicillin, a common antibiotic, because of its potential to help control the disease by affecting a brain chemical called glutamate. Surprisingly, the baby's irritability improved within 2 days of starting amoxicillin, and the improvement lasted for several months. However, the seizures persisted until another medication, perampanel, was added. This combination controlled the baby's seizures for over 3 months. Unfortunately, the baby passed away at 13 months due to complications from the disease. However, doctors believe that drugs like amoxicillin and perampanel could be promising treatments for managing symptoms of Alexander disease and other similar brain conditions in the future, especially where excess glutamate plays a role in the damage. This case suggests that these treatments may help control irritability and seizures, offering hope for better management of this challenging disease.
I型亚历山大病(AxD)在生命的最初几年表现为阵发性神经退行性变、难治性癫痫和脑病,预后较差。虽然尚无治疗方法,但有一例成年亚历山大病患者接受头孢曲松治疗后症状有轻度改善,这是因为头孢曲松与导致该病发病机制的突变胶质纤维酸性蛋白(GFAP)相互作用。我们描述了一名2个月大开始出现易激惹的患者,最初归因于胃食管反流。由于通过磁共振成像扫描检测到导水管狭窄继发脑积水,该患者在3个月大时接受了脑室腹腔分流术,但易激惹症状持续存在。5个月时,由于易激惹症状加重、出现异常眼球运动和癫痫发作,进行了新的脑部磁共振成像检查。此外还进行了基因检测。由于GFAP基因发生c.716G>A(p.Arg239His)突变,该患者被诊断为亚历山大病。由于易激惹症状加重且对左美丙嗪无反应,尝试用阿莫西林(80mg/kg/天)治疗以调节谷氨酸水平。该患者在48小时内易激惹症状显著改善,并在接下来的几个月持续好转。该患者每天频繁癫痫发作,对丙戊酸盐、氯硝西泮或苯巴比妥均无反应。在苯巴比妥基础上加用突触后AMPA受体拮抗剂吡仑帕奈后,患者无癫痫发作超过3个月。调节中枢神经系统谷氨酸水平的药物,包括β-内酰胺类抗生素和吡仑帕奈,可能在亚历山大病和其他以谷氨酸能兴奋性毒性为致病决定因素的神经退行性疾病的对症治疗中发挥重要作用。
亚历山大病是一种罕见且严重的疾病,会影响大脑,常导致儿童早期神经退行性变(脑损伤)、癫痫发作及其他问题。该病由一种名为GFAP的基因突变引起。目前尚无治愈方法,现有治疗主要集中在缓解症状。本文讨论了一名婴儿自幼出现易激惹和癫痫发作迹象的病例。经脑部扫描和基因检测,该婴儿被诊断为亚历山大病。尽管使用了多种药物治疗,该婴儿仍持续出现癫痫发作和易激惹症状。医生决定尝试使用常见抗生素阿莫西林,因其有可能通过影响一种名为谷氨酸的脑化学物质来帮助控制病情。令人惊讶的是,开始使用阿莫西林后2天内,婴儿的易激惹症状得到改善,且改善持续了数月。然而,癫痫发作一直持续,直到加用另一种药物吡仑帕奈。这两种药物联合使用使婴儿的癫痫发作得到控制超过3个月。不幸的是,该婴儿在13个月时因该病并发症去世。然而,医生认为像阿莫西林和吡仑帕奈这样的药物未来可能是治疗亚历山大病和其他类似脑部疾病症状的有前景的治疗方法,尤其是在谷氨酸过量导致损伤的情况下。该病例表明这些治疗方法可能有助于控制易激惹和癫痫发作,为更好地管理这种具有挑战性的疾病带来了希望。