Suppr超能文献

脑肌酸缺乏症:一组可治疗的智力发育障碍

Cerebral creatine deficiencies: a group of treatable intellectual developmental disorders.

作者信息

Stockler-Ipsiroglu Sylvia, van Karnebeek Clara D M

机构信息

Division of Biochemical Diseases, Department of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, Canada.

出版信息

Semin Neurol. 2014 Jul;34(3):350-6. doi: 10.1055/s-0034-1386772. Epub 2014 Sep 5.

Abstract

Currently there are 91 treatable inborn errors of metabolism that cause intellectual developmental disorders. Cerebral creatine deficiencies (CDD) comprise three of these: arginine: glycine amidinotransferase [AGAT], guanidinoacetate methyltransferase [GAMT], and X-linked creatine transporter deficiency [SLC6A8]. Intellectual developmental disorder and cerebral creatine deficiency are the hallmarks of CDD. Additional clinical features include prominent speech delay, autism, epilepsy, extrapyramidal movement disorders, and signal changes in the globus pallidus. Patients with GAMT deficiency exhibit the most severe clinical spectrum. Myopathy is a distinct feature in AGAT deficiency. Guanidinoacetate (GAA) is the immediate product in the creatine biosynthetic pathway. Low GAA concentrations in urine, plasma, and cerebrospinal fluid are characteristic diagnostic markers for AGAT deficiency, while high GAA concentrations are characteristic markers for GAMT deficiency. An elevated ratio of urinary creatine /creatinine excretion serves as a diagnostic marker in males with SLC6A8 deficiency. Treatment strategies include oral supplementation of high-dose creatine-monohydrate for all three CDD. Guanidinoacetate-reducing strategies (high-dose ornithine, arginine-restricted diet) are additionally employed in GAMT deficiency. Supplementation of substrates for intracerebral creatine synthesis (arginine, glycine) has been used additionally to treat SLC6A8 deficiency. Early recognition and treatment improves outcomes. Normal outcomes in neonatally ascertained siblings from index families with AGAT and GAMT deficiency suggest a potential benefit of newborn screening for these disorders.

摘要

目前有91种可治疗的导致智力发育障碍的先天性代谢缺陷病。脑肌酸缺乏症(CDD)包括其中三种:精氨酸:甘氨酸脒基转移酶[AGAT]、胍乙酸甲基转移酶[GAMT]和X连锁肌酸转运体缺乏症[SLC6A8]。智力发育障碍和脑肌酸缺乏是CDD的主要特征。其他临床特征包括明显的语言发育迟缓、自闭症、癫痫、锥体外系运动障碍以及苍白球信号改变。GAMT缺乏症患者表现出最严重的临床症状谱。肌病是AGAT缺乏症的一个显著特征。胍乙酸(GAA)是肌酸生物合成途径中的直接产物。尿液、血浆和脑脊液中GAA浓度低是AGAT缺乏症的特征性诊断标志物,而GAA浓度高是GAMT缺乏症的特征性标志物。尿肌酸/肌酐排泄率升高是男性SLC6A8缺乏症的诊断标志物。治疗策略包括对所有三种CDD口服补充高剂量的一水肌酸。对于GAMT缺乏症,还采用降低胍乙酸的策略(高剂量鸟氨酸、限制精氨酸饮食)。此外,还使用补充脑内肌酸合成的底物(精氨酸、甘氨酸)来治疗SLC6A8缺乏症。早期识别和治疗可改善预后。在患有AGAT和GAMT缺乏症的索引家族中,新生儿确诊的同胞预后正常,这表明对这些疾病进行新生儿筛查可能有益。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验