• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

婴儿型亚历山大病对阿莫西林和吡仑帕奈的反应。

Response to amoxicillin and perampanel in infantile Alexander disease.

作者信息

Boronat Susana, Turon-Viñas Eulalia, Mac Manus Noel, Diaz-Gomez Asuncion, Vicente Mónica, Ros-Castelló Victoria, Sierra-Marcos Alba

机构信息

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.

出版信息

Epilepsia Open. 2024 Dec;9(6):2505-2509. doi: 10.1002/epi4.13077. Epub 2024 Nov 6.

DOI:10.1002/epi4.13077
PMID:39503736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11633705/
Abstract

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.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ac3/11633705/b1a998869b91/EPI4-9-2505-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ac3/11633705/b1a998869b91/EPI4-9-2505-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ac3/11633705/b1a998869b91/EPI4-9-2505-g001.jpg
摘要

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。

通俗易懂的总结

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。

相似文献

1
Response to amoxicillin and perampanel in infantile Alexander disease.婴儿型亚历山大病对阿莫西林和吡仑帕奈的反应。
Epilepsia Open. 2024 Dec;9(6):2505-2509. doi: 10.1002/epi4.13077. Epub 2024 Nov 6.
2
Leukodystrophy with Macrocephaly, Refractory Epilepsy, and Severe Hyponatremia-The Neonatal Type of Alexander Disease.大头脑白质营养不良伴难治性癫痫和严重低钠血症——亚历山大病的新生儿型。
Genes (Basel). 2024 Mar 11;15(3):350. doi: 10.3390/genes15030350.
3
Symptomatic care of late-onset Alexander disease presenting with area postrema-like syndrome with prednisolone; a case report.泼尼松龙治疗以延髓后区样综合征为表现的晚发型亚历山大病的对症治疗:病例报告。
BMC Pediatr. 2022 Jul 13;22(1):412. doi: 10.1186/s12887-022-03468-y.
4
Efficacy and Safety of adjunctive Perampanel in a prospective, real-world, Phase IV study in Indian patients aged ≥12 years for Treatment of focal-onset Epilepsy: Study 508.在一项针对≥12 岁的印度局灶性癫痫患者的前瞻性、真实世界、四期研究中,附加用吡仑帕奈的疗效和安全性:研究 508。
Epilepsia Open. 2024 Jun;9(3):940-950. doi: 10.1002/epi4.12885. Epub 2024 Mar 16.
5
A case of severe Alexander disease with de novo c. 239 T > C, p.(F80S), in GFAP.一例患有新发GFAP基因c.239 T>C、p.(F80S)突变的严重亚历山大病病例。
Brain Dev. 2018 Aug;40(7):587-591. doi: 10.1016/j.braindev.2018.03.002. Epub 2018 Mar 21.
6
Alexander disease with mild dorsal brainstem atrophy and infantile spasms.伴有轻度脑桥背侧萎缩和婴儿痉挛症的亚历山大病
Brain Dev. 2013 May;35(5):441-4. doi: 10.1016/j.braindev.2012.06.009. Epub 2012 Jul 20.
7
Neonatal Alexander Disease: Novel GFAP Mutation and Comparison to Previously Published Cases.新生儿亚历山大病:新型胶质纤维酸性蛋白突变及与既往报道病例的比较
Neuropediatrics. 2018 Aug;49(4):256-261. doi: 10.1055/s-0038-1649500. Epub 2018 May 25.
8
GFAP variants leading to infantile Alexander disease: Phenotype and genotype analysis of 135 cases and report of a de novo variant.导致婴儿型亚历山大病的 GFAP 变异:135 例病例的表型和基因型分析及新发变异报告。
Clin Neurol Neurosurg. 2021 Aug;207:106754. doi: 10.1016/j.clineuro.2021.106754. Epub 2021 Jun 10.
9
PERPRISE: A prospective non-interventional study of PERampanel as only adjunctive treatment in patients with PRImary or SEcondarily generalized tonic-clonic seizures: First interim analysis.PERPRISE:普瑞巴林作为原发性或继发性全面强直-阵挛发作患者的唯一附加治疗的前瞻性非干预性研究:首次中期分析。
Epilepsia Open. 2024 Jun;9(3):926-939. doi: 10.1002/epi4.12869. Epub 2024 Mar 4.
10
GFAP mutations, age at onset, and clinical subtypes in Alexander disease.GFAP 突变、发病年龄和 Alexander 病的临床亚型。
Neurology. 2011 Sep 27;77(13):1287-94. doi: 10.1212/WNL.0b013e3182309f72. Epub 2011 Sep 14.

本文引用的文献

1
Efficacy of perampanel in pediatric epilepsy with known and presumed genetic etiology.佩南朋在已知和推测具有遗传病因的儿科癫痫中的疗效。
Ann Clin Transl Neurol. 2023 Aug;10(8):1374-1382. doi: 10.1002/acn3.51828. Epub 2023 Jun 16.
2
Beneficial Effect of Phenytoin and Carbamazepine on Gene Expression and Mutant GFAP Folding in a Cellular Model of Alexander's Disease.苯妥英钠和卡马西平对亚历山大病细胞模型中基因表达和突变型胶质纤维酸性蛋白折叠的有益作用。
Front Pharmacol. 2021 Dec 7;12:723218. doi: 10.3389/fphar.2021.723218. eCollection 2021.
3
Antisense therapy in a rat model of Alexander disease reverses GFAP pathology, white matter deficits, and motor impairment.
反义疗法在亚历山大病大鼠模型中可逆转 GFAP 病理学、白质缺陷和运动障碍。
Sci Transl Med. 2021 Nov 17;13(620):eabg4711. doi: 10.1126/scitranslmed.abg4711.
4
GFAP variants leading to infantile Alexander disease: Phenotype and genotype analysis of 135 cases and report of a de novo variant.导致婴儿型亚历山大病的 GFAP 变异:135 例病例的表型和基因型分析及新发变异报告。
Clin Neurol Neurosurg. 2021 Aug;207:106754. doi: 10.1016/j.clineuro.2021.106754. Epub 2021 Jun 10.
5
Perampanel Improves Cortical Myoclonus and Disability in Progressive Myoclonic Epilepsies: A Case Series and a Systematic Review of the Literature.吡仑帕奈改善进行性肌阵挛癫痫中的皮质肌阵挛和残疾:病例系列及文献系统评价
Front Neurol. 2021 Mar 24;12:630366. doi: 10.3389/fneur.2021.630366. eCollection 2021.
6
Alexander Disease Modeling in Zebrafish: An In Vivo System Suitable to Perform Drug Screening.亚历山大病斑马鱼模型构建:一种适合进行药物筛选的体内系统。
Genes (Basel). 2020 Dec 11;11(12):1490. doi: 10.3390/genes11121490.
7
The role of astrocytic glutamate transporters GLT-1 and GLAST in neurological disorders: Potential targets for neurotherapeutics.星形胶质细胞谷氨酸转运体 GLT-1 和 GLAST 在神经紊乱中的作用:神经治疗学的潜在靶点。
Neuropharmacology. 2019 Dec 15;161:107559. doi: 10.1016/j.neuropharm.2019.03.002. Epub 2019 Mar 6.
8
Modulation of the expression of genes related to the system of amyloid-beta metabolism in the brain as a novel mechanism of ceftriaxone neuroprotective properties.头孢曲松通过调节脑内淀粉样β代谢相关基因表达发挥神经保护作用的新机制。
BMC Neurosci. 2018 Apr 19;19(Suppl 1):13. doi: 10.1186/s12868-018-0412-5.
9
Alexander disease: an astrocytopathy that produces a leukodystrophy.亚历山大病:一种可导致脑白质营养不良的星形细胞病。
Brain Pathol. 2018 May;28(3):388-398. doi: 10.1111/bpa.12601.
10
Ceftriaxone attenuates glutamate-mediated neuro-inflammation and restores BDNF in MPTP model of Parkinson's disease in rats.头孢曲松减轻谷氨酸介导的神经炎症,并恢复大鼠帕金森病MPTP模型中的脑源性神经营养因子。
Pathophysiology. 2017 Jun;24(2):71-79. doi: 10.1016/j.pathophys.2017.02.001. Epub 2017 Feb 10.