Lithium citrate reduces excessive intra-cerebral N-acetyl aspartate in Canavan disease

被引:32
作者
Assadi, Mitra [1 ]
Janson, Christopher [2 ]
Wang, Dah-Jyuu [3 ]
Goldfarb, Olga
Suri, Neeti [3 ]
Bilaniuk, Larissa [3 ]
Leone, Paola [1 ]
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Ctr Cell & Gene Therapy, Camden, NJ 08103 USA
[2] Univ Minnesota, Minneapolis, MN 55455 USA
[3] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
关键词
Canavan disease; NAA; Lithium; HIGH-AFFINITY; IN-VIVO; HEALTHY-INDIVIDUALS; SODIUM VALPROATE; BRAIN; INCREASES; RAT; ACETYLASPARTATE; NEURONS; EXCITOTOXICITY;
D O I
10.1016/j.ejpn.2009.11.006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Our group has previously reported the first clinical application of lithium in a child affected by Canavan disease. In this study, we aimed to assess the effects of lithium on N-acetyl aspartate (NAA) as well as other end points in a larger cohort. Six patients with clinical, laboratory and genetic confirmation of Canavan disease were recruited and underwent treatment with lithium. The battery of safety and efficacy testing performed before and after sixty days of treatment included Gross Motor Function Testing (GMFM), Magnetic Resonance Imaging (MRI) Proton Magnetic Spectroscopy (H-MRS) as well as blood work. The medication was safe without any clinical or laboratory evidence for toxicity. Parental reports indicated improvement in alertness and social interactions. GMFM did not show statistically significant improvement in motor development. H-MRS documented an overall drop in NAA which was statistically significant in the basal ganglia. T1 measurements recorded on MRI studies suggested a mild improvement in myelination in the frontal white matter after treatment. Diffusion Tensor Imaging was available in two patients and suggested micro-structural improvement in the corpus callosum. The results suggest that lithium administration may be beneficial in patients with Canavan disease. (C) 2009 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:354 / 359
页数:6
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