Suppr超能文献

苯丙酮尿症的脑白质病变。

White matter pathology in phenylketonuria.

机构信息

Department of Psychology, The University of Melbourne, Melbourne, Vic. 3010, Australia.

出版信息

Mol Genet Metab. 2010;99 Suppl 1:S3-9. doi: 10.1016/j.ymgme.2009.10.005.

Abstract

Early-treated phenylketonuria (PKU) is associated with a range of neuropsychological impairments. Proposed mechanisms for these impairments include dopamine depletion and white matter pathology. Neuroimaging studies demonstrate high-signal intensity in the periventricular white matter in most PKU patients, which can extend into subcortical and frontal regions in more severe cases. A review of histopathology and neuroimaging studies reveals that diffuse white matter pathology in untreated PKU patients is likely to reflect hypomyelination (lack of myelin formation), while in early-treated patients white matter abnormalities observed on magnetic resonance imaging (MRI) is likely to reflect intramyelinic edema. Research demonstrates that this pathology is associated with metabolic control and may be reversed with adherence to a strict low-phenylalanine (Phe) diet. While the functional significance of white matter pathology in PKU is not certain, there is some evidence that these abnormalities are associated with functional impairments when the pathology extends into subcortical and frontal regions.

摘要

早期治疗的苯丙酮尿症(PKU)与一系列神经心理障碍有关。这些损伤的提出的机制包括多巴胺耗竭和白质病变。神经影像学研究表明,大多数 PKU 患者的脑室周围白质信号强度较高,在更严重的情况下,可延伸至皮质下和额叶区域。对组织病理学和神经影像学研究的回顾表明,未经治疗的 PKU 患者弥漫性白质病变可能反映了少突胶质细胞发育不全(髓鞘形成不足),而在早期治疗的患者中,磁共振成像(MRI)上观察到的白质异常可能反映了髓鞘内水肿。研究表明,这种病变与代谢控制有关,通过坚持严格的低苯丙氨酸(Phe)饮食,可能会逆转。虽然 PKU 中白质病变的功能意义尚不确定,但有一些证据表明,当病变延伸到皮质下和额叶区域时,这些异常与功能障碍有关。

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